Joe Leigh Simpson
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Biology
Joe Leigh Simpson's Degrees
- Doctorate Medicine Stanford University
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(Suggest an Edit or Addition)Joe Leigh Simpson's Published Works
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Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- Chromosomal microarray versus karyotyping for prenatal diagnosis. (2012) (989)
- Obstetrics: Normal and Problem Pregnancies (1986) (981)
- The International Glossary on Infertility and Fertility Care, 2017. (2017) (794)
- Preventing preterm births: analysis of trends and potential reductions with interventions in 39 countries with very high human development index (2012) (505)
- The International Glossary on Infertility and Fertility Care, 2017†‡§ (2017) (453)
- Heritable aspects of endometriosis. I. Genetic studies. (1980) (435)
- Lack of relation of increased malformation rates in infants of diabetic mothers to glycemic control during organogenesis (1988) (367)
- The FMR1 premutation and reproduction. (2007) (357)
- First-trimester screening for trisomies 21 and 18 (2003) (353)
- Abnormal sexual differentiation and neoplasia. (1987) (349)
- Incidence of spontaneous abortion among normal women and insulin-dependent diabetic women whose pregnancies were identified within 21 days of conception. (1988) (346)
- Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data (2002) (337)
- Genetics of primary ovarian insufficiency: new developments and opportunities (2015) (334)
- Cytogenetic results from the U.S. collaborative study on CVS (1992) (311)
- Metabolic Control and Progression of Retinopathy: The Diabetes in Early Pregnancy Study (1995) (301)
- Are obese women at higher risk for producing malformed offspring? (1994) (298)
- Association of extreme first-trimester free human chorionic gonadotropin-beta, pregnancy-associated plasma protein A, and nuchal translucency with intrauterine growth restriction and other adverse pregnancy outcomes. (2004) (243)
- Ovarian differentiation and gonadal failure. (1999) (241)
- The absence of a relation between the periconceptional use of vitamins and neural-tube defects. National Institute of Child Health and Human Development Neural Tube Defects Study Group. (1989) (230)
- Preimplantation genetic diagnosis reduces pregnancy loss in women aged 35 years and older with a history of recurrent miscarriages. (2005) (227)
- NOBOX homeobox mutation causes premature ovarian failure. (2007) (221)
- Research agenda for preterm birth: recommendations from the March of Dimes. (2005) (215)
- Heritability and molecular genetic studies of endometriosis. (2000) (211)
- First-trimester screening for trisomies 21 and 18. (2004) (208)
- Over a decade of experience with preimplantation genetic diagnosis: a multicenter report. (2004) (202)
- A randomized comparison of transcervical and transabdominal chorionic-villus sampling. The U.S. National Institute of Child Health and Human Development Chorionic-Villus Sampling and Amniocentesis Study Group. (1992) (200)
- Isolating fetal cells from maternal blood. Advances in prenatal diagnosis through molecular technology. (1993) (178)
- Klinefelter syndrome: Expanding the phenotype and identifying new research directions (2003) (177)
- Transcription factor FIGLA is mutated in patients with premature ovarian failure. (2008) (177)
- Cell-free fetal DNA in maternal blood: kinetics, source and structure. (2005) (167)
- Forty years of IVF. (2018) (165)
- Physiological reduction in fasting plasma glucose concentration in the first trimester of normal pregnancy: the diabetes in early pregnancy study. (1998) (161)
- Frequency of diabetes mellitus in mothers of probands with gestational diabetes: possible maternal influence on the predisposition to gestational diabetes. (1985) (161)
- Maternal Serum Screening for Fetal Down Syndrome in Women Less Than 35 Years of Age Using Alpha-Fetoprotein, hCG, and Unconjugated Estriol: A Prospective 2-Year Study (1992) (154)
- Moderate caffeine use and the risk of spontaneous abortion and intrauterine growth retardation (1993) (137)
- Cross-Country Individual Participant Analysis of 4.1 Million Singleton Births in 5 Countries with Very High Human Development Index Confirms Known Associations but Provides No Biologic Explanation for 2/3 of All Preterm Births (2016) (136)
- Growth differentiating factor-9 mutations may be associated with premature ovarian failure. (2007) (132)
- First trimester prenatal diagnosis of trisomy 21 in fetal cells from maternal blood (1992) (129)
- Circulating cell-free DNA: A novel biomarker for response to therapy in ovarian carcinoma (2006) (128)
- Heritable aspects of endometriosis (1980) (121)
- Genetics of the female reproductive ducts. (2000) (119)
- Heritage aspects of endometriosis. II. Clinical characteristics of familial endometriosis. (1980) (118)
- Micronutrients and women of reproductive potential: required dietary intake and consequences of dietary deficiency or excess. Part I – Folate, Vitamin B12, Vitamin B6 (2010) (115)
- Interlaboratory comparison of fetal male DNA detection from common maternal plasma samples by real-time PCR. (2004) (114)
- Elevated pregnancy losses at high and low extremes of maternal glucose in early normal and diabetic pregnancy: evidence for a protective adaptation in diabetes. (2005) (110)
- Substandard application of preimplantation genetic screening may interfere with its clinical success. (2007) (105)
- The Diabetes in Early Pregnancy Study: beta-hydroxybutyrate levels in type 1 diabetic pregnancy compared with normal pregnancy. NICHD-Diabetes in Early Pregnancy Study Group (DIEP). National Institute of Child Health and Development. (1998) (105)
- Low fetal loss rates after ultrasound-proved viability in early pregnancy. (1987) (105)
- A previously unrecognized X-linked syndrome of dysmorphia. (1975) (105)
- Causes of fetal wastage. (2007) (100)
- Evidence of skewed X-chromosome inactivation in 47,XXY and 48,XXYY Klinefelter patients. (2001) (98)
- Genetics in obstetrics and gynecology (1982) (98)
- Late First-Trimester Invasive Prenatal Diagnosis: Results of an International Randomized Trial (2004) (96)
- Genes, chromosomes, and reproductive failure. (1980) (96)
- Transformations and losses of urea nitrogen after application to flooded rice (1984) (94)
- Cytogenetic analysis of 531 Chinese women with premature ovarian failure. (2012) (93)
- Parental decision following prenatal diagnosis of fetal chromosome abnormality. (1988) (92)
- Declining insulin requirement in the late first trimester of diabetic pregnancy. (2001) (91)
- Disorders of sexual differentiation: Etiology and clinical delineation (1976) (91)
- Noninvasive Determination of Fetal RhD Status Using Fetal DNA in Maternal Serum and PCR (1999) (90)
- Somatic DNA alterations in endometriosis: high frequency of chromosome 17 and p53 loss in late-stage endometriosis. (2002) (88)
- PGDIS Position Statement on the Transfer of Mosaic Embryos 2019. (2019) (85)
- Shared HLA antigens and reproductive performance among Hutterites. (1983) (84)
- Sequential Pathways of Testing After First-Trimester Screening for Trisomy 21 (2004) (83)
- Micronutrients and women of reproductive potential: required dietary intake and consequences of dietary deficienty or excess. Part II - Vitamin D, Vitamin A, Iron, Zinc, Iodine, Essential Fatty Acids (2011) (82)
- Circulating trophoblastic cells provide genetic diagnosis in 63 fetuses at risk for cystic fibrosis or spinal muscular atrophy. (2012) (82)
- Analyses of GDF9 mutation in 100 Chinese women with premature ovarian failure. (2007) (78)
- Pregnancy-Associated Plasma Protein A, Free β-hCG, Nuchal Translucency, and Risk of Pregnancy Loss (2004) (78)
- Predictive value, sensitivity, and specificity of ultrasonic targeted imaging for fetal anomalies in gravid women at high risk for birth defects. (1985) (77)
- Rare event selection of fetal nucleated erythrocytes in maternal blood by flow cytometry. (1996) (76)
- Diabetes in pregnancy, Northwestern University series (1977-1981). I. Prospective study of anomalies in offspring of mothers with diabetes mellitus. (1983) (76)
- Endometrial adenocarcinoma: genetic analysis suggesting heritable site-specific uterine cancer. (1992) (74)
- Cell-free fetal DNA and intact fetal cells in maternal blood circulation: implications for first and second trimester non-invasive prenatal diagnosis. (2002) (74)
- Genetically determined sex-reversal in 46,XY humans (1978) (74)
- Gonadal dysgenesis in individuals with apparently normal chromosomal complements: tabulation of cases and compilation of genetic data. (1971) (73)
- Isolated fetal choroid plexus cysts and trisomy 18: a review and meta-analysis. (1995) (73)
- Genetic and Phenotypic Heterogeneity in Ovarian Failure (2008) (72)
- Increased heterogeneity of chromosome 17 aneuploidy in endometriosis. (1999) (71)
- Fetal Cells in the Maternal Circulation: Isolation by Multiparameter Flow Cytometry and Confirmation by Polymerase Chain Reaction (1991) (70)
- CSB-PGBD3 Mutations Cause Premature Ovarian Failure (2015) (68)
- The genetics of polycystic ovary syndrome. (2004) (68)
- Chorionic villus sampling safety. Report of World Health Organization/EURO meeting in association with the Seventh International Conference on Early Prenatal Diagnosis of Genetic Diseases, Tel-Aviv, Israel, May 21, 1994. (1996) (66)
- Genetic amniocentesis in twin gestations. (1980) (66)
- Chorionic mosaicism: Association with fetal loss but not with adverse perinatal outcome (1992) (66)
- Genetics of endometriosis: heritability and candidate genes. (2004) (65)
- Vitamin A and birth defects. (1997) (65)
- Over a decade of experience with preimplantation genetic diagnosis. (2004) (63)
- Adverse outcomes of planned and unplanned pregnancies among users of natural family planning: a prospective study. (1997) (62)
- Integration of microarray technology into prenatal diagnosis: counselling issues generated during the NICHD clinical trial (2012) (60)
- Evaluating Progestogens for Preventing Preterm birth International Collaborative (EPPPIC): meta-analysis of individual participant data from randomised controlled trials (2021) (58)
- Gonadal dysgenesis and abnormalities of the human sex chromosomes: current status of phenotypic-karyotypic correlations. (1975) (58)
- Heritable aspects of uterine anomalies. II. Genetic analysis of Müllerian aplasia. (1983) (57)
- Gender verification of female athletes (2000) (57)
- Pseudovaginal perineoscrotal hypospadias (1972) (56)
- Detection of chromosomal aneuploidy in endometriosis by multi-color fluorescence in situ hybridization (FISH) (1997) (56)
- Mutation analysis of NOBOX homeodomain in Chinese women with premature ovarian failure. (2009) (56)
- Gender verification in the Olympics. (2000) (56)
- Prenatal diagnosis with use of fetal cells isolated from maternal blood: five-color fluorescent in situ hybridization analysis on flow-sorted cells for chromosomes X, Y, 13, 18, and 21. (1998) (55)
- Birth defects and assisted reproductive technologies. (2014) (54)
- Invasive procedures for prenatal diagnosis: any future left? (2012) (53)
- Quantity versus quality: Optimal methods for cell-free DNA isolation from plasma of pregnant women (2006) (52)
- FALSE-NEGATIVE FINDING ON CHORIONIC VILLUS SAMPLING (1986) (51)
- Sex ratio associated with timing of insemination and length of the follicular phase in planned and unplanned pregnancies during use of natural family planning. (1998) (51)
- Adverse effects of human leukocyte antigen-DR sharing on fertility: a cohort study in a human isolate. (1985) (51)
- What next for preimplantation genetic screening? Randomized clinical trial in assessing PGS: necessary but not sufficient. (2008) (50)
- First birth following spindle transfer for mitochondrial replacement therapy: hope and trepidation. (2017) (50)
- Abnormalities of human sex chromosomes (1974) (50)
- Prenatal diagnosis by use of fetal cells isolated from maternal blood. (1995) (50)
- Preimplantation genetic diagnosis (PGD) for heritable neoplasia. (2005) (49)
- A solution pathway for preterm birth: accelerating a priority research agenda (2013) (47)
- Late First-Trimester Placental Disruption and Subsequent Gestational Hypertension/Preeclampsia (2005) (46)
- Gestational diabetes mellitus: a syndrome with phenotypic and genotypic heterogeneity. (1986) (46)
- Risk evaluation of CVS (1993) (45)
- HLA associations in endometriosis. (1984) (45)
- Novel variants in the SOHLH2 gene are implicated in human premature ovarian failure. (2014) (45)
- Choosing the best prenatal screening protocol. (2005) (44)
- Fetal cells in maternal blood: NIFTY clinical trial interim analysis (1999) (44)
- ULTRASOUND MARKERS FOR FETAL CHROMOSOMAL DEFECTS (1996) (43)
- Gender Verification in Competitive Sports (1993) (42)
- Heritable aspects of uterine anomalies. I. Three familial aggregates with Müllerian fusion anomalies. (1983) (42)
- Genetic Basis of Endometriosis (2004) (42)
- Sol-gel preparation of transparent silica glass (1984) (42)
- Risk of neural tube defects in relation to maternal fertility and fertility drug use (1990) (41)
- Medical examination for health of all athletes replacing the need for gender verification in international sports. The International Amateur Athletic Federation Plan. (1992) (41)
- Timing of conception and the risk of spontaneous abortion among pregnancies occurring during the use of natural family planning. (1995) (40)
- Translocations are infrequent among couples having repeated spontaneous abortions but no other abnormal pregnancies. (1989) (40)
- Genetics of endometriosis. (2003) (40)
- Intact fetal cells in maternal plasma: are they really there? (2003) (39)
- Chromosomal microarray versus karyotyping for prenatal diagnosis (2013) (39)
- Fetal surgery for myelomeningocele: promise, progress, and problems. (1999) (38)
- Cancers of the breast and female genital system: search for recessive genetic factors through analysis of human isolate. (1981) (38)
- Gonadal dysgenesis as an autosomal recessive condition. (1969) (38)
- Fetus-placenta-newborn☆ (1995) (37)
- Gonadal and statural determinants on the X chromosome and their relationship to in vitro studies showing prolonged cell cycles in 45,X; 46,X,del(X)(p11); 46,X,del(X)(q13); and 46,X,del(X)(q22) fibroblasts. (1981) (37)
- Spermicides, hormonal contraception and congenital malformations (1990) (37)
- Chromosome analysis of ectopic human conceptuses. (1981) (36)
- Moral attitudes and beliefs among couples pursuing PGD for sex selection. (2010) (36)
- Heritability and Molecular Genetic Studies of Endometriosis (2002) (35)
- Gonadal (ovarian) dysgenesis in 46,XX individuals: frequency of the autosomal recessive form. (1996) (34)
- Lack of association between antiphospholipid antibodies and first-trimester spontaneous abortion: prospective study of pregnancies detected within 21 days of conception. (1998) (33)
- Analysis of LHX8 mutation in premature ovarian failure. (2008) (33)
- Children born after preimplantation genetic diagnosis show no increase in congenital anomalies. (2010) (32)
- Developing a national collaborative study system for rare genetic diseases (2008) (31)
- Parental chromosomal rearrangements associated with repetitive spontaneous abortions. (1981) (30)
- Chorionic villus sampling for first-trimester prenatal diagnosis: Northwestern University program. (1985) (30)
- Preimplantation diagnosis of genetic and chromosomal disorders (1994) (30)
- Chorionic villus sampling in continuing pregnancies. II. Cytogenetic reliability. (1986) (29)
- Genetically Determined Sex‐Reversal in 46, XY Humans (1979) (29)
- Maternal serum alpha-fetoprotein screening: low and high values for detection of genetic abnormalities. (1986) (29)
- Celebrating preimplantation genetic diagnosis of p53 mutations in Li-Fraumeni syndrome. (2001) (29)
- Genetics Studies in Incomplete Müllerian Fusion (1984) (28)
- Genetic heterogeneity in neural tube defects. (1991) (27)
- Novel NR5A1 Missense Mutation in Premature Ovarian Failure: Detection in Han Chinese Indicates Causation in Different Ethnic Groups (2013) (27)
- Association of 8q22.3 locus in Chinese Han with idiopathic premature ovarian failure (POF). (2012) (27)
- Severity of abnormality influences decision to terminate pregnancies affected with fetal neural tube defects. (1994) (27)
- Prenatal effects of maternal-fetal HLA compatibility. (1987) (27)
- The reproductive option of sex selection. (1999) (26)
- Heritability and candidate genes for endometriosis. (2003) (26)
- Good clinical practice advice: Prediction of preterm labor and preterm premature rupture of membranes (2019) (26)
- Transcription factor SOHLH1 potentially associated with primary ovarian insufficiency. (2015) (26)
- Genetic testing of embryos: a critical need for data. (2005) (25)
- Mutation analysis of NANOS3 in 80 Chinese and 88 Caucasian women with premature ovarian failure. (2007) (25)
- Preimplantation genetic diagnosis to improve pregnancy outcomes in subfertility. (2012) (25)
- Abnormal sexual differentiation in humans. (1982) (25)
- FMR1 Premutation Is an Uncommon Explanation for Premature Ovarian Failure in Han Chinese (2014) (24)
- Good clinical practice advice: Antenatal corticosteroids for fetal lung maturation (2019) (24)
- Paternal gonadal mosaicism detected in a couple with recurrent abortions undergoing PGD: FISH analysis of sperm nuclei proves valuable. (2004) (24)
- Developing a core outcome set for future infertility research: an international consensus development study (2020) (24)
- Associations between adverse perinatal outcome and serially obtained second- and third-trimester maternal serum alpha-fetoprotein measurements. (1995) (24)
- American Academy of Pediatrics Committee on Genetics: New issues in newborn screening for phenylketonuria and congenital hypothyroidism. (1982) (23)
- Protein expression profiling of endometriosis: validation of 2-mm tissue microarrays. (2004) (23)
- Cell-free fetal DNA and maternal serum analytes for monitoring embryonic and fetal status. (2013) (23)
- Chronic renal disease, myotonic dystrophy, and gonadoblastoma in XY gonadal dysgenesis (1982) (23)
- XY gonadal dysgenesis: Genetic heterogeneity based upon clinical observations, H-Y antigen status and segregation analysis (2004) (23)
- Oocyte-specific G-protein-coupled receptor 3 (GPR3): no perturbations found in 82 women with premature ovarian failure (first report). (2008) (23)
- Changing indications for preimplantation genetic diagnosis (PGD) (2001) (23)
- Syndromes of camptodactyly, multiple ankylosis, facial anomalies, and pulmonary hypoplasia. (1978) (22)
- Familial urinary tract anomalies. (1970) (22)
- Unintended pregnancies in women delivering at 18 South American hospitals. NFP-ECLAMC Group. Latin American Collaborative Study of Congenital Malformations. (1998) (22)
- First‐trimester biochemical and molecular diagnoses using chorionic villi: High accuracy in the U.S. collaborative study (1992) (22)
- Fetal surgery for myelomeningocele? (2002) (21)
- Impact of an Academic–Community Partnership in Medical Education on Community Health: Evaluation of a Novel Student-Based Home Visitation Program (2014) (21)
- Current status of preimplantation diagnosis (1997) (21)
- XX Sex Reversal in the Human (1994) (20)
- Chorionic villus sampling in continuing pregnancies. I. Low fetal loss rates in initial 109 cases. (1986) (20)
- Good clinical practice advice: Management of twin pregnancy (2019) (20)
- Unclassified sex cord-stromal tumors of the ovary: a report of eight cases. (1998) (20)
- Infectious processes: an infrequent cause of first trimester spontaneous abortions. (1996) (20)
- Hypostatic ulcers in 47,XXY Klinefelter's syndrome (1983) (20)
- Chromosomal mosaicism. (1972) (20)
- Fetomaternal transfusion depends on amount of chorionic villi aspirated but not on method of chorionic villus sampling. (1990) (19)
- Nuclear chromosomal localization in human preimplantation embryos: correlation with aneuploidy and embryo morphology. (2004) (19)
- Triploidy (69,XXY) in a liveborn infant. (1972) (19)
- Preimplantation genetic diagnosis. (1992) (19)
- Isolating fetal cells in the maternal circulation. (1995) (19)
- Good clinical practice advice: Iron deficiency anemia in pregnancy (2019) (18)
- Abnormalities of the Müllerian and Wolffian duct systems. (1978) (18)
- Overview of Preimplantation Genetic Diagnosis (PGD): Historical Perspective and Future Direction. (2018) (18)
- Inability to detect fetal metaphases in flow-sorted lymphocyte cultures based on maternal-fetal HLA differences. (1993) (18)
- Nonsense mutation of EMX2 is potential causative for uterus didelphysis: first molecular explanation for isolated incomplete müllerian fusion. (2015) (18)
- Growth disadvantage of 45,X and 46,X,del (X) (p11) fibroblasts (1988) (18)
- Genetic counseling in translocations. (2002) (17)
- Pregnancy and the timing of intercourse. (1995) (17)
- Low maternal serum α-fetoprotein and perinatal outcome (1987) (17)
- Genetic and Nongenetic Causes of Pregnancy Loss (2009) (17)
- Relationship between Y-chromosome length and first-trimester spontaneous abortions. (1983) (17)
- Mutations in the conserved domain of SRY are uncommon in XY gonadal dysgenesis (1992) (17)
- Carrier screening for cystic fibrosis: implications for obstetric and gynecologic practice. (1991) (17)
- Genetic Programming in Ovarian Development and Oogenesis (2007) (17)
- Gender testing in the Olympics. (1986) (16)
- Pseudovaginal perineoscrotal hypospadias (PPSH) in sibs. (1971) (16)
- Sister chromatid exchange frequency in directly prepared cytotrophoblasts: demonstration of in vivo deoxyribonucleic acid damage in pregnant women who smoke cigarettes. (1991) (16)
- Cell-free fetal DNA in maternal blood: evolving clinical applications. (2004) (16)
- Prenatal genetic testing and treatment for congenital adrenal hyperplasia. (2019) (16)
- Comparison of serum placental protein hormone levels in diabetic and normal pregnancy. (1989) (16)
- Preimplantation diagnosis and other modern methods for prenatal diagnosis (2017) (16)
- Rapid chromosome analysis with the use of spontaneously dividing cells derived from umbilical cord blood (fetal and neonatal). (1989) (16)
- Assessing congenital anomalies after preimplantation genetic diagnosis (1996) (15)
- Lack of heritability in ovarian germ cell malignancies. (1994) (15)
- The Olympic Games and Athletic Sex Assignment. (2016) (15)
- Evaluation of a Culture System for Enrichment of CD34+ Hematopoietic Progenitor Cells Present in Maternal Blood (2002) (15)
- Detecting fetal DNA from dried maternal blood spots: another step towards broad scale non-invasive prenatal genetic screening and feasible testing. (2003) (15)
- Ultrasonic induction of sister chromatid exchanges in human lymphocytes (1981) (14)
- Professional self-regulation for preimplantation genetic diagnosis: experience of the American Society for Reproductive Medicine and other professional societies. (2006) (14)
- Prenatal diagnosis of congenital muscular dystrophy producing arthrogryposis. (1985) (14)
- Transabdominal chorionic villus sampling for first-trimester prenatal diagnosis. (1989) (14)
- Role of Preimplantation Genetic Diagnosis (PGD) in Current Infertility Practice (2010) (14)
- Genetic screening for cystic fibrosis. (2002) (14)
- Good clinical practice advice: First trimester screening and prevention of pre‐eclampsia in singleton pregnancy (2019) (13)
- Teratology and Drugs in Pregnancy (2009) (13)
- Abnormalities of human sex chromosomes. I. A ring Y without mosaiciam. (1973) (13)
- Public objections to designer babies and cloning in USA: not quite what was expected. (2003) (13)
- INCREASED MALE-TO-FEMALE SEX RATIO AMONG HLA-DR COMPATIBLE PREGNANCIES (1985) (13)
- Endocervical fetal trophoblast for prenatal genetic diagnosis (2006) (13)
- Verification of Early Pregnancy Tests in a Multicenter Trial (1987) (12)
- Male pseudohermaphroditism: Genetics and Clinical delineation (1978) (12)
- Periconceptional use of multivitamins and the prevalence of neural-tube defects. (1990) (12)
- Current progress in preimplantation genetic diagnosis (1993) (12)
- Relationship between congenital anomalies and contraception (1985) (12)
- Vitamins, folic acid and neural tube defects: Comments on investigations in the United States (1991) (12)
- Genes and chromosomes that cause female infertility. (1985) (12)
- Fetal Cells in Maternal Blood: Prospects for Noninvasive Prenatal Diagnosis. Proceedings of a conference. Arlington, Virginia, September 27-29, 1993. (1994) (12)
- Spatial Positioning of All 24 Chromosomes in the Lymphocytes of Six Subjects: Evidence of Reproducible Positioning and Spatial Repositioning following DNA Damage with Hydrogen Peroxide and Ultraviolet B (2015) (12)
- Characterization of an unbalanced de novo rearrangement by microsatellite polymorphism typing and by fluorescent in situ hybridization. (1995) (12)
- Bilateral anorchia: discordance in monozygotic twins. (1971) (12)
- 9 Screening for fetal and genetic abnormalities (1991) (12)
- Best Practice & Research Clinical Obstetrics and Gynaecology (2012) (12)
- Why are we still talking about chromosomal heteromorphisms? (2017) (11)
- Down syndrome is not increased in offspring of natural family planning users (case control analysis) (1995) (11)
- Elevated levels of total (maternal and fetal) beta-globin DNA in maternal blood from first trimester pregnancies with trisomy 21. (2007) (11)
- Chorionic villus sampling (CVS): World health organization european regional office (WHO/EURO) meeting statement on the use of CVS in prenatal diagnosis (1992) (11)
- Genetic Aspects of Gynecologic Disorders Occurring in 46,XX Individuals (1972) (11)
- Vitamins During Pregnancy and Neural Tube Defects (1990) (11)
- Risky Business: Meeting the Structural Needs of Transdisciplinary Science. (2017) (11)
- Genetic counseling and genetic services in obstetrics and gynecology: implications for educational goals and clinical practice. (1981) (11)
- Is cell-free fetal DNA from maternal blood finally ready for prime time? (2012) (11)
- Drug ingestion during pregnancy: infrequent exposure in a contemporary United States sample. National Institute of Child Health and Human Development Diabetes in Early Pregnancy Study Group. (1989) (10)
- Chromosome territory repositioning induced by PHA-activation of lymphocytes: A 2D and 3D appraisal (2015) (10)
- Drugs and Environmental Agents in Pregnancy and Lactation: Embryology, Teratology, Epidemiology (2007) (10)
- Hormonal and genetic basis of sexual differentiation disorders and hot topics in endocrinology : proceedings of the 2nd world conference (2013) (10)
- Unexplained elevated maternal serum alpha-fetoprotein is not predictive of adverse perinatal outcome in an indigent urban population. (1992) (10)
- Disorders of the Gonads, Genital Tract, and Genitalia (2013) (10)
- Timing of intercourse. (1995) (10)
- Next-generation sequencing for preimplantation genetic diagnosis. (2013) (10)
- Genetics of diabetes mellitus (DM) and anomalies in offspring of diabetic mothers. (1978) (10)
- Can the Oxytocin Challenge Test Serve as the Primary Method for Managing High‐Risk Pregnancies? (1975) (10)
- Failure to detect polycystic kidneys in utero by second trimester ultrasonography (1982) (10)
- NAT2 and GSTM1 DNA polymorphisms: increased GSTM1 (active) genotypes in endometriosis (2002) (10)
- Phenotypic-Karyotypic Correlations of Gonadal Determinants: Current Status and Relationship to Molecular Studies (1987) (10)
- Further evidence that infection is an infrequent cause of first trimester spontaneous abortion. (1996) (10)
- Genetic Forms of Gonadal Dysgenesis in 46,XX and 46,XY Individuals (1983) (9)
- Xq;autosome translocation in POF: Xq27.2 deletion resulting in haploinsufficiency for SPANX (2011) (9)
- Medicine: Blastomeres and stem cells (2006) (9)
- Recovery and amplification of placental RNA from dried maternal blood spots: utility for non-invasive prenatal diagnosis. (2006) (9)
- Cancer mortality in a human isolate. (1980) (9)
- Methodological Problems in Determining Fetal Loss Rates: Relevance to Chorionic Villi Sampling (1985) (9)
- Good clinical practice advice: Thyroid and pregnancy (2019) (9)
- Ethnic specificity of variants of the ESR1, HK3, BRSK1 genes and the 8q22.3 locus: no association with premature ovarian failure (POF) in Serbian women. (2014) (9)
- Molecular approach to common causes of female infertility. (2002) (9)
- Knowledge of likely time of ovulation and contraceptive use in unintended pregnancies (1999) (9)
- The Prenatal Diagnosis of Genetic Disorders (1982) (9)
- A general approach to genetic counseling. (2002) (8)
- Aetiology of Pregnancy Failure (1992) (8)
- Preterm births in countries with a very high human development index – Authors' reply (2013) (8)
- Before the beginning: the genetic risk of a couple aiming to conceive. (2019) (8)
- Testicular feminisation and inguinal hernia. (1973) (8)
- Genetic screening for donors in artificial insemination. (1981) (8)
- Interstitial deletion 46,XY,del(1)(q23q25) (1982) (8)
- Low fetal loss rates after ultrasound-proved viability in early pregnancy (1988) (8)
- Cell-free DNA versus intact fetal cells for prenatal genetic diagnostics: what does the future hold? (2015) (8)
- Fetal cells in maternal blood. Overview and historical perspective. (1994) (8)
- Toward scientific discussion of human reproductive cloning. (2003) (8)
- Workshop report: evaluation of genetic and epigenetic risks associated with assisted reproductive technologies and infertility. (2007) (8)
- Genetics of female infertility due to anomalies of the ovary and mullerian ducts. (2014) (8)
- Maternal serum alpha-fetoprotein screening in 1987. (1987) (8)
- Preimplantation genetic testing to reduce preterm births in assisted reproductive technology (2020) (7)
- Prenatal diagnosis and 47,XXY (2013) (7)
- Evaluation and Development of a System for Automated Preparation of Blood Specimens for Cytogenetic Analysis (1989) (7)
- Low maternal serum alpha-fetoprotein and perinatal outcome. (1987) (7)
- Prenatal genetic diagnosis. (1971) (7)
- Trisomy 21 and maternal age of menopause: does reproductive age rather than chronological age influence risk of nondisjunction? (2004) (7)
- Verification of early pregnancy tests in a multicenter trial. (1987) (7)
- Florida International University Herbert Wertheim College of Medicine. (2010) (7)
- Enabling precision medicine in neonatology, an integrated repository for preterm birth research (2018) (7)
- Metastatic rhabdomyosarcoma presenting as an isolated lateral rectus restriction. (1999) (7)
- Necessity of Formal Genetic Screening in Artificial Insemination by Donor (1983) (7)
- Association of N-Acetyltransferase 2 (NAT2) genetic polymorphism resulting in decreased capacity to detoxify aromatic amines in women with endometriosis (1998) (7)
- Genetic Causes of Premature Ovarian Failure (POF). (2012) (7)
- Intrauterine growth retardation in osteogenesis imperfecta. (1978) (6)
- ANTENATAL DIAGNOSIS OF CYTOGENETIC ABNORMALITIES (1980) (6)
- The Effect of the Elapsed Time Between Blood Draw and Processing on the Recovery of Fetal Cells From Maternal Blood (2004) (6)
- Diagnosis of trisomy 18 using spontaneously dividing cells from fetal umbilical cord blood: a novel approach for rapid late second and third trimester prenatal diagnosis. (1990) (6)
- Developing a core outcome set for future infertility research: an international consensus development study. (2020) (6)
- Good clinical practice advice: Micronutrients in the periconceptional period and pregnancy (2019) (6)
- Pericentric X chromosome ascertained during antenatal diagnosis (1980) (6)
- Hypermodal cells in amniotic fluid cultures: frequency, interpretation, and clinical significance. (1982) (6)
- Olympic row over sex testing (1992) (6)
- Genetic Causes of Spontaneous Abortion (1993) (6)
- The prenatal diagnosis of genetic disorders. (1982) (6)
- Quantitative DNA perturbations of p53 in endometriosis: analysis of American and Icelandic cases. (2005) (6)
- Hereditary factors in obstetrics and gynecology. (1969) (6)
- Screening for down syndrome (2002) (6)
- Elevated alpha-fetoprotein and acetylcholinesterase associated with hydrocele. (1984) (6)
- Could cloning become permissible (2007) (5)
- Progressive idiopathic clitoral hypertrophy in a child: a previously undescribed type of female pseudohermaphroditism. (1971) (5)
- Genetics of Spontaneous Abortions (2014) (5)
- Segregation analysis and genetic counseling when both parents carry balanced chromosomal translocations. (1991) (5)
- CHAPTER 5 – Genetic Programming in Ovarian Development and Oogenesis (2000) (5)
- Current Controversies in Prenatal Diagnosis 3: Gene editing should replace embryo selection following PGD (2019) (5)
- Genetics of Premature Ovarian Failure: New Developments in Etiology (2017) (5)
- Pocket Companion to Accompany Obstetrics: Normal and Problem Pregnancies (2002) (5)
- Transvaginal chorionic villus sampling using transabdominal ultrasound guidance: a new technique for first-trimester prenatal diagnosis. (1993) (5)
- Abnormalities of human sex chromosomes. II. Turner's syndrome associated with the mosaicism 45,X-46, XX-p. (1971) (5)
- Pocket Companion to Obstetrics: Normal & Problem Pregnancies (1999) (5)
- Anaphase lag as the most likely mechanism for monosomy X in direct cytotrophoblasts but not in mesenchymal core cells from the same villi. (1990) (5)
- Antenatal detection of genetic disorders. (1976) (5)
- Re: Update on MSAFP Policy Statement from the ASHG. (1990) (5)
- Maternal serum screening for fetal down syndrome using alpha-fetoprotein, human chorionic gonadotrophin, and unconjugated estriol in adolescents (1993) (5)
- Analysis for possible linkage between the loci for the Waardenburg syndrome and various blood groups and serological traits (1974) (5)
- Developmental anomaly resembling the trisomy 18 syndrome. (1969) (5)
- Preterm birth: A clinical enigma and a worldwide public health concern (2020) (5)
- Cytogenetic analysis of a case of "13q- syndrome" (46,XX,del 13) using banding techniques. (1980) (5)
- Generalized dysmorphia of a similar type in two unrelated babies. (1975) (4)
- Isolation and genetic analysis of fetal nucleated red blood cells from maternal blood: the Baylor College of Medicine experience. (1996) (4)
- Clinical implications of chromosomal inversions. A pericentric inversion in No. 18 segregating in a family ascertained through an abnormal proband. (1983) (4)
- Transvaginal chorionic villus sampling using transabdominal ultrasound guidance (1992) (4)
- Smith’s Recognizable Patterns of Human Malformation, 6th ed., Kenneth Lyons Jones (Ed.). Elsevier Saunders, Philadelphia, Pennsylvania (2005), 1, Price: $93.00 (2007) (4)
- Novel NR 5 A 1 Missense Mutation in Premature Ovarian Failure : Detection in Han Chinese Indicates Causation in Different Ethnic Groups (2016) (4)
- Ovarian Dysgenesis and Premature Ovarian Failure Caused by X Chromosomal Abnormalities (2009) (4)
- Where Are the Genes That Cause Endometriosis? (2005) (4)
- Prenatal Diagnosis for Pediatricians (1980) (4)
- A patient with the Larsen syndrome. (1975) (4)
- Do contraceptive methods pose fetal risks? (1985) (4)
- Stability of sex chromosome mosaicism. (1980) (4)
- Genetic Counseling and Genetic Screening (2007) (4)
- Good clinical practice advice: Role of ultrasound in the management of twin pregnancy (2019) (4)
- Novel non-synonymous mutation in the transforming growth factor beta binding protein-like (TB) domain of the fibrillin-1 (FBN1) gene in a Han Chinese family with Marfan syndrome (MFS). (2007) (4)
- Clinical Implications of Chromosomal Inversions (2008) (4)
- Analysis for amniotic fluid crystallization in second-trimester amniocentesis. (1979) (4)
- 289 Sex and Gender in Sport: Fallacy of the “Level Playing Field” (2010) (4)
- Telomere length and aneuploidy: clinical and biological insights into human preimplantation embryos. (2014) (4)
- PRENATAL DIAGNOSIS OF CYTOGENETIC DISORDERS (1976) (4)
- Closing the folate gap in reproductive-age women (2010) (4)
- Diabetes Mellitus: Preventing Anomalies Through Maternal Metabolic Intervention (1986) (4)
- Risk of recurrent spontaneous abortion for pregnancies discovered in the fifth week of gestation (1994) (4)
- Gender Verification and the Next Olympic Games-Reply (1993) (3)
- Abnormalities of human sex chromosomes. 3. Duplication in the long arm of the Y chromosome (45,X-46,XYg+) in Y-gonadal dysgenesis. (1971) (3)
- Genetic Control of Sex Determination (1987) (3)
- Novel non-invasive prenatal diagnosis as related to congenital adrenal hyperplasia. (2011) (3)
- Yury Verlinsky (01/09/1943–16/07/2009): pioneer in CVS, PGD and hESC (2009) (3)
- Gender Testing in the Olympics (1987) (3)
- Genetics of Oocyte Depletion (1997) (3)
- Fertilisation involving ageing gametes, major birth defects, and Down's syndrome (2002) (3)
- Comprar Obstetrics. Normal And Problem Pregnancies (Online And Print) 7th Ed. | Steven G. Gabbe | 9780323321082 | Elsevier Internacional (2016) (3)
- Male Pseudohermaphroditism Due to Androgen Insensitivity or 5α-Reductase Deficiency (2009) (3)
- XX Gonadal Dysgenesis and Premature Ovarian Failure in 46,XX Individuals (2009) (3)
- Chorionic villus sampling: First trimester prenatal diagnosis (1986) (3)
- Mutations in mitochondrial histidyl tRNA synthetase (HARS2) is not associated with premature ovarian failure in a cohort of 69 patients (2012) (3)
- Contraception and Congenital Malformations (2009) (3)
- Repeated suboptimal pregnancy outcome. (1981) (3)
- Anencephaly in Three Siblings (1969) (3)
- Multifetal Reduction in High-Order Gestations: A Nonelective Procedure? (1996) (3)
- Practical Preimplantation Genetic Testing (2020) (3)
- Florida International University: Development and Accreditation of Miami’s Public College of Medicine (2009) (3)
- FIGO good practice recommendations for reducing preterm birth and improving child outcomes (2021) (3)
- Timing of conception and the risk of spontaneous abortion among pregnancies during use of natural family planning. (1994) (2)
- Prenatal cytogenetic screening (1995) (2)
- Assessing Loss Rates in the Preimplantation Stages of Gestation (1991) (2)
- Absence of Close Linkage Between the Locus for Xg and the Locus for Anhidrotic Ectodermal Dysplasia 1 (1969) (2)
- Diagnosis and management of the infant with genital ambiguity. (1977) (2)
- Two male sibs with a previously unrecognized syndrome: facial dysmorphia, hyperextensibility of joints, clinodactyly, growth retardation and mental retardation. (1975) (2)
- Lower nephron nephrosis in pregnancy. (1952) (2)
- The frequency and spectrum of congenital anomalies in natural family planning users in South America: No increase in a case-control study (1997) (2)
- Can Pregnancies Be Achieved in Premature Ovarian Insufficiency? (2019) (2)
- Gonadal Dysgenesis in 46,XY Females (XY Gender-Reversal) (2009) (2)
- Detection of genomic imbalances by comparative genomic hybridization in Chinese fetuses with malformations. (2007) (2)
- Screening for fetal and genetic abnormalities. (1991) (2)
- Risk factors associated with transcervical CVS losses (1992) (2)
- Further comments on amniocentesis in twin gestations. (1983) (2)
- Polygenic/Multifactorial Inheritance (2009) (2)
- Does unexplained second‐trimester (15 to 20 weeks' gestation) maternal serum α‐fetoprotein elevation presage adverse perinatal outcome? Pitfalls and preliminary studies with late second‐ and third‐trimester maternal serum α‐fetoprotein (1992) (2)
- Hypermodal cells, hypomodal cells, and repetitive abortions. (1986) (2)
- Clinical Genetics: A Source Book for Physicians (1980) (2)
- In vitro fertilization with preimplantation genetic screening. (2007) (2)
- Sister chromatid exchanges after exposure to ultrasound and mitomycin C. (1984) (2)
- Response from the Editors: First birth following spindle transfer. (2017) (2)
- 9.2 Advantages and Disadvantages of Competing in International Markets (2020) (2)
- Sister chromatid exchange (SCE) frequencies differ between directly prepared cytotrophoblasts and cultured mesenchymal core cells (1991) (2)
- Improving assisted reproductive technology pregnancy rates: excluding aneuploid and interrogating euploid embryos. (2015) (2)
- Localization of the nucleolar organizer by computer-aided analysis of a variant no. 21 in a human isolate (1979) (2)
- Antenatal diagnosis of chromosomal disorders. (1980) (2)
- Genetic factors in stillbirths (2011) (2)
- Genetic diseases in pregnancy : maternal effects and fetal outcome (1981) (2)
- Delayed fertilization and Down's syndrome. (1977) (2)
- Prospects for prevention of neural tube defects by vitamin supplementation. (1993) (2)
- Genetics of common disorders causing female infertility: part I (2001) (2)
- Preface: Genetic screening and counseling. (2010) (2)
- Abnormalities of human sex chromosomes. VI. Monozygotic twins with the complement 48,XXXY. (1974) (2)
- Three different, non-mosaic sex chromosome abnormalities (direct cytotrophoblasts, mesenchymal core cultures, and abortus skin fibroblasts): implications for elucidating chorionic villi mosaicism. (1989) (2)
- Letter: Bilateral teratoma of testis in 2 brothers with 47,XXY Klinefelter's syndrome. (1976) (2)
- I1 Clinical challenges in application of prenatal technologies (2013) (2)
- Invasive Prenatal Genetic Techniques (2009) (2)
- Antenatal diagnosis of cytogenetic abnormalities. (1981) (2)
- Direct analysis of uncultured cytotrophoblastic cells from second- and third-trimester placentas: An accurate and rapid method for detection of fetal chromosome abnormalities (1990) (2)
- Commentary re: Causes and estimated incidences of sex-chromosome misdiagnosis in preimplantation genetic diagnosis of aneuploidy. (2016) (2)
- IMPACT OF EXPANDED CARRIER SCREENING (ECS) ON UPTAKE OF PREIMPLANTATION GENETIC TESTING FOR MONOGENIC DISORDERS (PGT-M) (2019) (2)
- Reproductive medicine in a shrinking world. (1996) (1)
- GENDER VERIFICATION AND THE NEXT OLYMPIC GAMES. AUTHOR'S REPLIES (1993) (1)
- FDA approves 23andMe gene carrier test (2015) (1)
- Disorders of gonadal development in humans. (1989) (1)
- Down syndrome and natural family planning (1996) (1)
- [Late first-trimester invasive prenatal diagnosis--secondary publication. An international randomized trial]. (2005) (1)
- Section 4: Fetoscopy and fetal tissue sampling (1981) (1)
- Methods of Culture (2014) (1)
- Book ReviewMajor Sex-Determining Genes (1980) (1)
- Ovarian Dysgenesis and Related Genetic Disorders (1987) (1)
- Genetic screening and counseling (2002) (1)
- Strategies and Indications for Preimplantation Genetic Testing for Monogenic Disorders (PGT-M) (2020) (1)
- Seattle Metropolitan Chapter (SMC) (1999) (1)
- Clarification of ECLAMC/NFP case control study (1996) (1)
- Preimplantation genetic diagnosis (PGD) for a balanced reciprocal translocation reveals a high proportion (85%) of abnormal embryos. (2001) (1)
- GENETICS FOR THE OBSTETRICIAN‐GYNECOLOGIST: QUESTIONS AND ANSWERS (1976) (1)
- A prospective study of adverse pregnancy outcomes among planned and unplanned pregnancies in natural family planning users. (1996) (1)
- Mammalian Sex Determination (2008) (1)
- Noninvasive screening for prenatal genetic diagnosis. (1995) (1)
- Abnormalities of human autosomes. I. Ambigous genitalia associated with a translocation 46,XY, t(Cq+;Cq-). (1971) (1)
- Caffeine Use During Pregnancy: How Much Is Safe?-Reply (1993) (1)
- Comprar Obstetrics: Normal and Problem Pregnancies | Mark Landon | 9780443069307 | Churchill Livingstone (2007) (1)
- Noninvasive fetal diagnosis (2012) (1)
- Letter: Cytogenetic confirmation of failure of polar-body extrusion. (1973) (1)
- Jumping 22q11.21 Translocation: Clinical Consequences and Counseling in an Oligospermic but Otherwise Healthy Adult Male (2005) (1)
- PGD : a model to evaluate efficacy? Authors' reply (2006) (1)
- Preimplantation Genetic Testing in the Future (2020) (1)
- Are we ready for universal genetic screening? (2010) (1)
- Increased sister chromatid exchanges in human cell lines characterized by monosomy X or structural abnormalities of the X chromosome (2004) (1)
- Preimplantation genetic diagnosis: Its time is now (2016) (1)
- Outcome of pregnancy in users of natural family planning. (1989) (1)
- Prenatal diagnosis of chromosomal abnormalities using maternal blood. (2002) (1)
- Author Correction: Enabling precision medicine in neonatology, an integrated repository for preterm birth research (2018) (1)
- More than we ever wanted to know about sex--should we be afraid to ask? (1979) (1)
- Fetoscopy, fetal-tissue sampling and the ESHRE guidelines on prenatal diagnosis. (1996) (1)
- Genital Duct Anomalies (2009) (1)
- FIGO good practice recommendations on the importance of registry data for monitoring rates and health systems performance in prevention and management of preterm birth (2021) (1)
- Diabetic control and fetal malformations. (1988) (1)
- Cover Story: Noninvasive screening for aneuploidy: who, when, and why? (2000) (1)
- GENETIC: GENETIC CAUSES OF PREMATURE OVARIAN FAILURE (POF) AND EARLY MENOPAUSE (2011) (1)
- Clinical Outcome of Preimplantation Genetic Testing (2020) (1)
- Anatomy of the Pelvis (1996) (1)
- Presidents' Page (1999) (1)
- Storms of Silence (1996) (1)
- Copyright and License Information (2020) (1)
- Germ Cell Failure and Ovarian Resistance: Human Genes and Disorders (2019) (1)
- True Method of Education (2014) (0)
- Abstracts From Invited Speakers (2007) (0)
- Hypogonadotropic and Hypergonadotropic Hypogonadism in Females: Disorders of Reproductive Ducts (2022) (0)
- Cultivation of Taste (2014) (0)
- Founder of the Normal School (2014) (0)
- Early amniocentesis had similar fetal loss/very preterm delivery rate, compared to late CVS, but more foot defects (2005) (0)
- Prevenire il deficit di acido folico nelle donne in età fertile (2011) (0)
- 7.2 Entrepreneurial Orientation (2020) (0)
- 8.5 Strategies for Getting Smaller (2020) (0)
- David L. Healy, M.D., Ph.D., 1948-2012. (2012) (0)
- 1.5 Contemporary Critique of Strategic Management (2020) (0)
- 11.2 Doing Well by Doing Good (2020) (0)
- First trimester prenatal treatment and molecular genetic diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) (1990) (0)
- Preimplantation genetic diagnosis: Which patients to test and other controversies (2009) (0)
- Preimplantation Genetic Testing (PGT) for Human Leukocyte Antigens (HLA) (PGT-HLA) (2020) (0)
- Fetal Wastage: Genetic Evaluation (2009) (0)
- REPETITIVE SPONTANEOUS ABORTION (1986) (0)
- Genetics of male pseudohermaphroditism and true hermaphroditism (1996) (0)
- The Journal ofln Vitro Fertilization and Embryo Transfer would like to thank all reviewers for their contri- butions to the Journal by listing their names in alphabetic order. (1986) (0)
- HBOC and Lynch syndrome testing: All in a day’s work (2018) (0)
- Call for Papers (2004) (0)
- 3.4 Evaluating the Industry (2020) (0)
- 9.5 Drivers of Success and Failure When Competing in International Markets (2020) (0)
- Single-cell genetic diagnosis: molecular methods and pitfalls (1994) (0)
- Major Components of Preimplantation Genetic Testing: Adjustment of Available Genetic Technology to PGT Practice (2020) (0)
- 3.1 Introduction (2020) (0)
- Chapter 3: Evaluating the External Environment (2020) (0)
- Chapter 6: Selecting Business-Level Strategies (2020) (0)
- P103S Missense Mutation in a Highly Conserved Region of Growth Differentiating Factor - 9 (GDF-9): Single Abnormality Among 62 Women With Premature Ovarian Failure (2005) (0)
- Maternal serum alpha-fetoprotein screening: promise not yet fulfilled. (1979) (0)
- 2.2 Vision, Mission, and Goals (2020) (0)
- Chapter 1: Mastering Strategy: Art and Science (2020) (0)
- Reviewer Acknowledgment (2013) (0)
- 8.1 Introduction (2020) (0)
- Chapter 33. Klinefelter Syndrome (2010) (0)
- 8.4 Implementing Corporate Strategy (2020) (0)
- 9.4 Types of International Strategies (2020) (0)
- 4.6 Conclusion (2020) (0)
- ACOG Clinical Guidelines at a Glance: Prenatal diagnostic testing for genetic disorder (2017) (0)
- 9.3 CAGE Framework (2020) (0)
- 11.3 Corporate Governance (2020) (0)
- Call for papers (1993) (0)
- 3.5 Mapping Strategic Groups (2020) (0)
- O-45. PGD of a cryptic translocation: implications for segregation products (2002) (0)
- The Genetics of Spontaneous Abortions (2020) (0)
- The President’s Page (1974) (0)
- 95018358 Trisomy 21 and maternal age of menopause: Does reproductive age rather than chronological age influence risk of nondisjunction? (1995) (0)
- Marker chromosomes in gonadal dysgenesis : avoiding unnecessary surgery (1992) (0)
- P-688: Oocyte specific G-protein coupled receptor-3 (GPR3) gene perturbations are not commonly involved in premature ovarian failure (2006) (0)
- Nuclear localization of chromosomes in blastomeres from human preimplantation embryos (2003) (0)
- Heritable Factors In Gynecologic Cancer (2009) (0)
- Vitamin a & birth defects (1998) (0)
- 4.1 Introduction (2020) (0)
- Medical Examination for Health of All Athletes Replacing the Need for Gender Verification in International Sports: The International Amateur Athletic Federation Plan (1992) (0)
- Sign Out: Chasing Cassandra (2005) (0)
- Medical Genetics: Principles and Practice (1982) (0)
- 2.5 Conclusion (2020) (0)
- Comprar Hormonal and Genetic Basis of Sexual Differentiation Disorders and Hot Topics in Endocrinology: Proceedings of the 2nd World Conference | New, Maria I. | 9781441980014 | Springer (2011) (0)
- P-921: Prevention of rhesus alloimmunization: Determination of paternal rhesus D zygosity by plasma DNA analysis prior to preimplantation genetic diagnosis (PGD) (2006) (0)
- Incomplete testicular feminization (1974) (0)
- 1937: Fluorescence In-Situ Hybridization of Sperm Consistent with Gonadal Mosaicism in a Male with Normal Karyotype: Transmission by ICSI Resulting in Recurrent Pregnancy Loss (2007) (0)
- Authors' reply (1992) (0)
- [Detection of fetal cells in maternal blood: towards a noninvasive prenatal diagnosis]. (1995) (0)
- Touch the void with Congress speaker: An introduction to Joe Simpson’s talk at Congress 2010 (2009) (0)
- Genética del síndrome de ovarios poliquísticos (2006) (0)
- 9.7 Conclusion (2020) (0)
- Epidermoid carcinoma of the cervix; a statistical study. (1951) (0)
- Mass Scale Biosensor Threat Diagnostic for In-Theater Defense Utilization (2012) (0)
- Prenatal Diagnosis and Treatment of Genetic Steroid Disorders (2019) (0)
- X International Congress of The Society for the Advancement of Contraception Manila, Philippines, 5–9 November 1998 Abstracts (in alphabetical order of author) (1998) (0)
- Invasive Diagnostic Procedures for Prenatal Genetic Diagnosis (2000) (0)
- Chapter 10: Executing Strategy through Organizational Design (2020) (0)
- SOMATIC DNA ALTERATIONS IN ENDOMETRIOSIS: HIGH FREQUENCY OF CHRO-CYP1A1, GSTM1, ENDOMETRIOSIS, SOUTH INDIAN WOMEN MOSOME 17 AND P53 LOSS IN LATE-STAGE ENDOMETRIOSIS (2002) (0)
- Occupational and Environmental Perspectives of Birth Defects (2002) (0)
- The Educator: THE MEANS OF ELEVATING THE PROFEESSION OF THE EDUCATOR IN PUBLIC ESTIMATION (2014) (0)
- Chapter 4: Evaluating the Internal Environment (2020) (0)
- True Character of the Educator (2014) (0)
- 6.2 Understanding Business-Level Strategy through “Generic Strategies” (2020) (0)
- 10.2 Why Organizational Design (2020) (0)
- C39 PGD and ethics: What limits should be assigned to the indications? (2010) (0)
- Hahn S., Holzgreve W. Fetal cells and fetal DNA in maternal blood: New developments for a new millennium. Basel: Karger, 2001:1–137. $85.25. (2002) (0)
- Genetic source of femininity. (1991) (0)
- Transabdominal chorionic villus sampling in a patient with a bicornuate uterus. (1989) (0)
- 3.6 Conclusion (2020) (0)
- The Subfertility Handbook: Early pregnancy loss (2010) (0)
- Study Guide for Obstetrics: Normal and Problem Pregnancies (1992) (0)
- 4.2 Managing Firm Resources (2020) (0)
- 11.4 Corporate Ethics and Social Responsibility (2020) (0)
- 1.6 Understanding the Strategic Management Process (2020) (0)
- Chapter 11: Leading an Ethical Organization: Corporate Governance, Corporate Ethics, and Social Responsibility (2020) (0)
- Novel Therapies for Treating Short Stature withCongenital Adrenal Hyperplasia (2011) (0)
- 7.7 Conclusion (2020) (0)
- 6.7 Stuck in the Middle (2020) (0)
- Chapter 9: Competing in International Markets (2020) (0)
- 1.4 The History of Strategic Management (2020) (0)
- 10.6 Legal Forms of Business (2020) (0)
- CV: Joe Leigh Simpson, M.D. (2011) (0)
- Maternal serum AFP screening: promise not yet fulfilled. (1979) (0)
- 2.1 Introduction (2020) (0)
- Editorial help (2004) (0)
- 8.6 Portfolio Planning and Corporate-Level Strategy (2020) (0)
- Chapter 2: Assessing Organizational Performance (2020) (0)
- The Educator: Connexion of Education with the Character and Position of the Educator (2014) (0)
- 4.5 Value Chain (2020) (0)
- LIST OF Contributors (2022) (0)
- CHAPTER 32 – Germ Cell Failure and Ovarian Resistance: Human Genes and Disorders (2003) (0)
- Female Sex Anomalies, by Cary M. Dougherty, M.D., and Rowena Spencer, M.D. New York/Evanston/San Francisco/London: Harper & Row, Publishers, 1972, 273 pp., $12.75 (1973) (0)
- 1.7 Conclusion (2020) (0)
- DNA microarrays: A promising new option for prenatal diagnosis (2007) (0)
- Noninvasive screening forprenatal genetic diagnosis (1995) (0)
- Genetics: Androgen insensitivity (2001) (0)
- 10.1 Introduction (2020) (0)
- 5.3 Strategic Issue Identification (2020) (0)
- 11.5 Contemporary Questions of Corporate Ethics (2020) (0)
- The Educator: Prize Essays on the Expediency and Means of Elevating the Profession of the Educator in Society (2008) (0)
- 6.5 Focused Cost Leadership and Focused Differentation (2020) (0)
- DTC genetic testing: What do you tell patients? (2009) (0)
- 4.3 Resource-Based View (2020) (0)
- Place of Preimplantation Genetic Testing (PGT) Among Available Options for Prevention of Genetic Disorders (2020) (0)
- 10.3 The Basic Building Blocks of Organizational Structure (2020) (0)
- The Educator: Education.—Moral Developement as the ground of Knowledge (2014) (0)
- 4.4 Intellectual Property & Isolating Mechanisms (2020) (0)
- Plan of a Normal School (2014) (0)
- Genetics In Obstetrics & Gynecology (1992) (0)
- Fetal movements and chromosome anomalies (1983) (0)
- 8.7 Conclusion (2020) (0)
- Genetic causes are responsible for most first trimester pregnancy losses (2000) (0)
- Selected papers from the 26th Annual Scientific Meeting of the (2008) (0)
- Number of Number of Median (range) Number of cells male female cells recovered and identified as cases cases analysed by FISHmale by FISH Centre (2003) (0)
- 5.2 SWOT Framework (2020) (0)
- Sign Out: Prenatal screening isn't perfect (2007) (0)
- Criblage du syndrome de down (2007) (0)
- 6.6 Best-Cost Strategy (2020) (0)
- Non-synonymous single nucleotide polymorphism in MCM8 decreased in a cohort of premature ovarian failure patients (2012) (0)
- Reply: PGD—a model to evaluate efficacy? (2006) (0)
- Reproducing Genetics (2015) (0)
- Comprar Obstetrics: Normal and Problem Pregnancies, 6th Edition | Deborah Driscoll | 9781437719352 | Saunders (2012) (0)
- Rapid noninvasive detection of fetal RhD in maternal serum of sensitized RhD-negative women by PCR (1998) (0)
- The Educator: The Educator a Foster Parent (2014) (0)
- Evaluation of chromosome 17 aneuploidy and p53 loss in endometriosis by fluorescence in situ hybridization (FISH). (2001) (0)
- Origin of Aneuploidy and Strategies Underlying Clinical Application of Preimplantation Genetic Testing for Chromosomal Disorders (PGT-A and PGT-SR) (2020) (0)
- 8.2 Corporate-Level Strategy Defined (2020) (0)
- Chapter 7: Innovation Strategies (2020) (0)
- Hypostatic ulcers in47,XXYKlinefelter's syndrome (1983) (0)
- Author Correction: Enabling precision medicine in neonatology, an integrated repository for preterm birth research (2018) (0)
- Major Components of Preimplantation Genetic Testing (2020) (0)
- Chapter-16 Intact Fetal Cells and Cell-free DNA in Maternal Blood: Definitive Nonivasive Prenatal Diagnosis (2006) (0)
- Making sense of the CF screening guidelines (2004) (0)
- 10.4 Creating an Organizational Structure (2020) (0)
- Court sides with Sandoz over Neupogen biosimilar (2015) (0)
- LETTERS TO THE EDITORTo the Editor (1979) (0)
- 7.3 Why Innovate (2020) (0)
- Robert G Edwards: visionary for preimplantantion genetic diagnosis (PGD) (2011) (0)
- Testicular feminization syndrome. (1969) (0)
- Autoradiographic studies of human chromosomes. 3. - The arm ratio of the late-replicating X. (1974) (0)
- Editorial and Production Teams (2020) (0)
- 6.3 Cost Leadership (2020) (0)
- Congenital adrenal hyperplasia (2021) (0)
- Principles of Human Genetics: Chromosomal and Single‐Gene Disorders (2008) (0)
- 6.1 Introduction (2020) (0)
- ANTENATAL DIAGNOSIS OF GENETIC DISORDERS (1981) (0)
- Chapter 13C – Preimplantation Diagnosis and Other Modern Methods for Prenatal Diagnosis (2014) (0)
- 6.8 Conclusion (2020) (0)
- LETTERS TO THE EDITORLetters to the editor (1979) (0)
- GENETIC: DO BIRTH DEFECTS INCREASE WITH ASSISTED REPRODUCTIVE TECHNOLOGIES? (2011) (0)
- Cytogenetic nomenclature. (1977) (0)
- Mutations in Man (1985) (0)
- 8.3 Diversification (2020) (0)
- 11.1 Introduction (2020) (0)
- The Sound of Gravity (2011) (0)
- Letter: Incomplete testicular feminization. (1974) (0)
- 5.1 Introduction (2020) (0)
- Developing a minimum data set, known as a core outcome set, for future infertility research (2020) (0)
- 3.3 Evaluating the General Environment (2020) (0)
- 1.2 What is Strategic Management (2020) (0)
- 10.5 Creating Organizational Control Systems (2020) (0)
- P53 perturbations in endometriosis detected by quantitative real-time PCR: further evidence of late somatic DNA alterations (2003) (0)
- Molecular profiling of endometriosis using tissue microarrays: Disease correlation with increased expression of estrogen receptor-α (ER-α) and decreased expression of progesterone receptor (PR) (2003) (0)
- Nature and Value of Education (2014) (0)
- Preface - Vol. 52 (2018) (0)
- Highlights of the XVIII FIGO World Congress (XML) (2006) (0)
- A quantitative and qualitative examination of couples wishing to pursue IVF with PGD for non-medical sex selection (2009) (0)
- The Educator: Expediency of rightly appreciating Education and its Professors (2014) (0)
- Abstract presented for the Twenty-third Annual Meeting of the Society of Gynecologic Oncologists March 15–18, 1992Endometrial adenocarcinoma: Genetic analysis indicating heritable site-specific uterine cancer (1992) (0)
- Genetics in Medicine (1987) (0)
- 10.7 Conclusion (2020) (0)
- Autoradiographic studies of human chromosomes. 3. Segregation of the no. 13 chromosomes in one family. (1969) (0)
- 6.4 Differentiation (2020) (0)
- Session 10 natural family planning (1995) (0)
- Frequency and clinical management of numerical and segmental mosaicism in embryo biopsies obtained for preimplantation genetic testing (PGT) (2020) (0)
- 7.1 Introduction (2020) (0)
- Maternal serum alpha-fetoprotein screening in adolescents (1991) (0)
- Reviewer Acknowledgment (2008) (0)
- Chapter 8: Selecting Corporate-Level Strategies (2020) (0)
- Turner's syndrome (1980) (0)
- 7.5 Implementing Innovation (2020) (0)
- 3.2 The Relationship between an Organization and its Environment (2020) (0)
- Cytogenetic, Teratogenic, and Miscellaneous Other Disorders Causing Male Pseudohermaphroditism or Germ-Cell Failure in Males (46,XY) and Females (46,XX) (2009) (0)
- Chapter 5: Synthesis of Strategic Issues and Analysis (2020) (0)
- Preimplantation Genetic Screening and Diagnostic Testing (2015) (0)
- Genetic History Taking and Counseling (2009) (0)
- 9.6 Options for Competing in International Markets (2020) (0)
- 2.3 Assessing Organizational Performance (2020) (0)
- 2.4 Competitive Advantage (2020) (0)
- Genetic Disorders of Human Sexual Development, by Leonard Pinsky, Robert P. Erickson, and R. Neil Schimke (2001) (0)
- The Influence of Maternal Hormones on the Fetus and Newborn Pediatric and Adolescent Endocrinology (2008) (0)
- 9.1 Introduction (2020) (0)
- Implementing Prenatal Carrier Screening for Cystic Fibrosis (2002) (0)
- Accessibility (HTML version) (2020) (0)
- Antenatal monitoring of genetic disorders. (1979) (0)
- Erroneous and unjust Conduct of Individuals and the Public concerning Education and its Professors (2014) (0)
- 7.4 Types of Innovation (2020) (0)
- ART and offspring anomalies: How concerned should we be? (2005) (0)
- 1.3 Intended, Emergent, and Realized Strategies (2020) (0)
- Verlinsky Y, Kuliev A. An Atlas of Preimplantation Genetic Diagnosis. New York: The Parthenon Publishing Group, 2000:1–174. (2001) (0)
- How frequent are chromosomal abnormalities in spontaneous abortuses? reassessment on the basis of chorionic villus vs. embryonic cultures (1985) (0)
- Safety of frozen semen. (1979) (0)
- R--short-limbed dwarfism. (1974) (0)
- 7.6 Responding to Innovation in the Market (2020) (0)
- Expanding Indications for Preimplantation Genetic Testing (PGT) – Impact on ART Practices (2020) (0)
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