Yury Verlinsky
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Russian geneticist
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Yury Verlinskybiology Degrees
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Biology
Yury Verlinsky's Degrees
- PhD Genetics Moscow State University
Why Is Yury Verlinsky Influential?
(Suggest an Edit or Addition)According to Wikipedia, Yury Verlinsky was a Russian-American medical researcher specializing in embryonic and cellular genetics . He is best known as a pioneer in prenatal diagnosis for detecting genetic and chromosomal disorders six weeks earlier than standard amniocentesis. The founding father of pre-implantation genetic diagnosis and embryo analysis prior to in-vitro fertilization , Verlinsky used his polar body biopsy technique to detect potential birth defects in offspring. It is now accepted worldwide as the standard for the most efficient and effective means of analyzing the chromosomal status of an embryo.
Yury Verlinsky's Published Works
Number of citations in a given year to any of this author's works
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
- Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage (2011) (489)
- Preimplantation diagnosis for Fanconi anemia combined with HLA matching. (2001) (389)
- Analysis of the first polar body: preconception genetic diagnosis. (1990) (349)
- Cytogenetic results from the U.S. collaborative study on CVS (1992) (311)
- Chromosomal abnormalities in a series of 6,733 human oocytes in preimplantation diagnosis for age-related aneuploidies. (2003) (246)
- Human embryonic stem cell lines with genetic disorders. (2008) (233)
- Morula-derived human embryonic stem cells. (2004) (216)
- Over a decade of experience with preimplantation genetic diagnosis: a multicenter report. (2004) (202)
- Mosaicism in the inner cell mass of human blastocysts. (1998) (180)
- Preimplantation HLA testing. (2004) (162)
- Preimplantation testing for chromosomal disorders improves reproductive outcome of poor-prognosis patients. (2005) (156)
- Frequency and distribution of chromosome abnormalities in human oocytes (2005) (153)
- Diagnosing and preventing inherited disease: Pregnancies following pre-conception diagnosis of common aneuploidies by fluorescent in-situ hybridization (1995) (143)
- Preimplantation genetic diagnosis for cancer predisposition. (2002) (127)
- Birth of healthy children after preimplantation diagnosis of common aneuploidies by polar body fluorescent in situ hybridization analysis. Preimplantation Genetics Group. (1996) (120)
- Preimplantation diagnosis for early-onset Alzheimer disease caused by V717L mutation. (2002) (117)
- Meiotic and mitotic nondisjunction: lessons from preimplantation genetic diagnosis. (2004) (113)
- Allele Dropout in Polar Bodies and Blastomeres (1998) (108)
- Preimplantation Diagnosis of Common Aneuploidies by the First- and Second-Polar Body FISH Analysis (1998) (108)
- Substandard application of preimplantation genetic screening may interfere with its clinical success. (2007) (105)
- Preconception and preimplantation diagnosis for cystic fibrosis (1992) (105)
- Cytogenetic results of chorionic villus sampling: high success rate and diagnostic accuracy in the United States collaborative study. (1990) (104)
- Pregnancies following pre-conception diagnosis of common aneuploidies by fluorescent in-situ hybridization. (1995) (95)
- Prevention of Age-Related Aneuploidies by Polar Body Testing of Oocytes (1999) (94)
- Preimplantation genetic diagnosis with HLA matching. (2004) (93)
- Preimplantation Diagnosis of Thalassemias (1998) (91)
- Preimplantation diagnosis and HLA typing for haemoglobin disorders. (2005) (88)
- Three-dimensional partial zona dissection for preimplantation genetic diagnosis and assisted hatching. (1999) (80)
- Human embryonic stem cell models of Huntington disease. (2009) (79)
- Preimplantation diagnosis for p53 tumour suppressor gene mutations. (2001) (78)
- Preimplantation diagnosis of single gene disorders by two-step oocyte genetic analysis using first and second polar body. (1997) (76)
- Neonatal Outcome of Preimplantation Genetic Diagnosis by Polar Body Removal: The First 109 Infants (2000) (73)
- Preconception genetic diagnosis of cystic fibrosis (1990) (70)
- Accuracy of Preimplantation Diagnosis of Single-Gene Disorders by Polar Body Analysis of Oocytes (1999) (70)
- Preimplantation diagnosis of common aneuploidies in infertile couples of advanced maternal age. (1996) (68)
- Practical Preimplantation Genetic Diagnosis (2005) (67)
- 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)
- Term birth after midtrimester hysterotomy and selective delivery of an acardiac twin. (1992) (64)
- Over a decade of experience with preimplantation genetic diagnosis. (2004) (63)
- Current features of preimplantation genetic diagnosis. (2002) (62)
- Nuclear transfer for full karyotyping and preimplantation diagnosis for translocations. (2002) (62)
- Is there any predictive value of first polar body morphology for embryo genotype or developmental potential? (2003) (61)
- Karyotyping of human oocytes by chromosomal analysis of the second polar bodies. (1999) (60)
- Analyses of 95 first-trimester spontaneous abortions by chorionic villus sampling and karyotype (1992) (60)
- Reliability of preimplantation diagnosis for single gene disorders (2001) (59)
- Association of red cell spherocytosis with deletion of the short arm of chromosome 8. (1987) (58)
- Reprogramming of human somatic cells by embryonic stem cell cytoplast. (2006) (57)
- Multiple micromanipulations for preimplantation genetic diagnosis do not affect embryo development to the blastocyst stage. (2006) (56)
- Thirteen years' experience of preimplantation diagnosis: report of the Fifth International Symposium on Preimplantation Genetics. (2004) (55)
- Birth of Healthy Children After Preimplantation Diagnosis of Thalassemias (1999) (55)
- Preimplantation Genetics: Improving Access to Stem Cell Therapy (2005) (55)
- Place of preimplantation diagnosis in genetic practice (2005) (55)
- Chromosomal abnormalities in the first and second polar body (2001) (54)
- A simplified and efficient method for obtaining metaphase chromosomes from individual human blastomeres. (1999) (53)
- Influence of maternal age on the outcome of PGD for aneuploidy screening in patients with recurrent implantation failure. (2005) (53)
- PRENATAL TAY-SACHS DIAGNOSIS BY CHORIONIC VILLI SAMPLING (1983) (49)
- Ultrasonographic detection of the second-trimester fetus with trisomy 18 and trisomy 21. (1990) (49)
- Polar body diagnosis of common aneuploidies by FISH (1996) (49)
- Effect of chromosomal translocations on the development of preimplantation human embryos in vitro. (2000) (49)
- Okadaic acid induces premature chromosome condensation reflecting the cell cycle progression in one‐cell stage mouse embryos (1993) (48)
- Polar body-based preimplantation diagnosis for X-linked disorders. (2002) (46)
- Preimplantation diagnosis for neurofibromatosis. (2002) (45)
- Risk evaluation of CVS (1993) (45)
- Preimplantation HLA typing with aneuploidy testing. (2006) (44)
- Impact of preimplantation genetic diagnosis for chromosomal disorders on reproductive outcome. (2008) (43)
- Three births after preimplantation genetic diagnosis for cystic fibrosis with sequential first and second polar body analysis. (1998) (41)
- Designer babies - are they a reality yet? Case report: simultaneous preimplantation genetic diagnosis for Fanconi anaemia and HLA typing for cord blood transplantation. (2000) (40)
- Prepregnancy genetic testing for age-related aneuploidies by polar body analysis. (1997) (40)
- Preimplantation Diagnosis of Genetic Diseases: A New Technique in Assisted Reproduction (1993) (40)
- Prepregnancy testing for single-gene disorders by polar body analysis. (1999) (39)
- PGD for all cystic fibrosis carrier couples: novel strategy for preventive medicine and cost analysis. (2010) (38)
- Current status of preimplantation diagnosis for single gene disorders. (2003) (37)
- Detection of aneuploidy in human oocytes and corresponding first polar bodies by fluorescent in situ hybridization (2005) (37)
- Cross‐hybridization of the chromosome 13/21 alpha satellite DNA probe to chromosome 22 in the prenatal screening of common chromosomal aneuploidies by fish (1995) (36)
- Obstetric outcomes in 102 pregnancies after preimplantation genetic diagnosis. (2000) (36)
- Preimplantation genetic diagnosis: technological advances to improve accuracy and range of applications. (2008) (35)
- Preimplantation HLA typing and stem cell transplantation: report of International Meeting, Cyprus, 27-8 March, 2004. (2004) (34)
- Preimplantation diagnosis for immunodeficiencies. (2007) (33)
- Pre-embryonic diagnosis for Sandhoff disease. (2006) (30)
- Preimplantation diagnosis of genetic and chromosomal disorders (1994) (30)
- Preimplantation genetic diagnosis (1996) (30)
- Preimplantation genetic diagnosis for familial dysautonomia. (2003) (29)
- Preimplantation diagnosis for sonic hedgehog mutation causing familial holoprosencephaly. (2003) (29)
- The role of preimplantation genetic diagnosis in women of advanced reproductive age (2003) (29)
- Allele dropout in sequential PCR and FISH analysis of single cells (cell recycling) (1996) (28)
- Fusion as the Etiology of Chimerism in Monochorionic Dizygotic Twins (2004) (28)
- Parthenogenetic activation of human oocytes by puromycin (1992) (27)
- Preimplantation polar body diagnosis. (1996) (27)
- Genetic testing of embryos: a critical need for data. (2005) (25)
- Homeobox gene expression in human oocytes and preembryos (1995) (24)
- Preimplantation diagnosis: a realistic option for assisted reproduction and genetic practice (2005) (24)
- Repository of human embryonic stem cell lines and development of individual specific lines using stembrid technology. (2006) (24)
- Preimplantation testing for phenylketonuria. (2001) (24)
- Preimplantation diagnosis for homeobox gene HLXB9 mutation causing Currarino syndrome (2005) (21)
- Current status of preimplantation diagnosis (1997) (21)
- Preimplantation genetic diagnosis for polycystic kidney disease. (2004) (21)
- Conversion and non-conversion approach to preimplantation diagnosis for chromosomal rearrangements in 475 cycles. (2010) (21)
- Viability of embryos following second polar body removal in a mouse model (1995) (20)
- Preimplantation Genetics (1991) (20)
- A microsurgical technique for enucleation of multipronuclear human zygotes. (2000) (20)
- Birth of a healthy girl after preimplantation gender determination using a combination of polymerase chain reaction and fluorescent in situ hybridization analysis. Preimplantation Genetics Group. (1996) (20)
- Obtaining metaphase spreads from single blastomeres for PGD of chromosomal rearrangements. (2007) (19)
- Duplication of the sperm genome by human androgenetic embryo production: towards testing the paternal genome prior to fertilization. (2007) (19)
- Micromanipulation and biopsy of polar bodies and blastomeres (2004) (18)
- The preimplantation genetic diagnosis of genetic diseases (1990) (18)
- Reliability of gender determination using the polymerase chain reaction (PCR) for single cells (1991) (18)
- Detection of translocations involving the Y‐chromosome in prospective prenatal screening of common chromosomal aneuploidies by FISH (1998) (17)
- Embryonic stem cells from morula. (2006) (17)
- Preimplantation diagnosis of autosomal dominant retinitis pigmentosum using two simultaneous single cell assays for a point mutation in the rhodopsin gene. (1998) (17)
- Preimplantation genetic diagnosis for the Kell genotype. (2003) (17)
- Visualization of Chromosomes in Single Human Blastomeres (1999) (16)
- Preembryonic diagnosis for sickle cell disease (2001) (16)
- Preimplantation diagnosis for aneuploidies in assisted reproduction. (2004) (16)
- Non-informative results and monosomies in PGD: the importance of a third round of re-hybridization. (2009) (15)
- Visualization and cytogenetic analysis of second polar body chromosomes following its fusion with a one-cell mouse embryo (1994) (15)
- Cytogenetic analysis of human somatic cell haploidization. (2005) (15)
- Clastogen-induced chromosomal breakage as a marker for first trimester prenatal diagnosis of Fanconi anemia (1986) (15)
- Preimplantation HLA typing (2008) (14)
- Editorial: Preimplantation Genetics (1998) (14)
- Isolation of cDNA libraries from individual human preimplantation embryos. (1998) (14)
- Prenatal diagnosis of 46,XX male fetuses. (1999) (14)
- Experience with Single Cell PCR in Preimplantation Genetic Diagnosis: How to Avoid Pitfalls (2001) (13)
- Preimplantation diagnosis for ornithine transcarbamylase deficiency. (2000) (12)
- Visualization of second polar body chromosomes in fertilized and artificially activated mouse oocytes treated with okadaic acid (1992) (12)
- Preimplantation diagnosis for aneuploidies using fluorescence in situ hybridization or comparative genomic hybridization. (2003) (12)
- Genetic Analysis of Human Embryos Prior to Implantation: Future Applications of In Vitro Fertilization in the Treatment and Prevention of Human Genetic Diseases (1987) (12)
- Designing babies: what the future holds. (2005) (12)
- Current progress in preimplantation genetic diagnosis (1993) (12)
- Expression of homeobox-containing genes in human preimplantation development and in embryos with chromosomal aneuploidies (1996) (12)
- Impact of meiotic and mitotic non-disjunction on generation of human embryonic stem cell lines. (2009) (11)
- Prenatal paternity testing with deoxyribonucleic acid techniques. (1996) (11)
- Preimplantation genetic diagnosis for Pelizaeus-Merzbacher disease with testing for age-related aneuploidies. (2006) (11)
- Micromanipulation of gametes and embryos in preimplantation genetic diagnosis and assisted fertilization. (1992) (11)
- Correlation between preimplantation genetic diagnosis for chromosomal aneuploidies and the efficiency of establishing human ES cell lines. (2009) (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)
- Human preimplantation diagnosis: needs, efficiency and efficacy of genetic and chromosomal analysis. (1994) (10)
- Preimplantation genetic diagnosis in assisted reproduction (2005) (10)
- Assessment of the Safety and Accuracy of Chorionic Villi Sampling in First Trimester Fetal Diagnosis (1985) (9)
- Preimplantation diagnosis for diseases with genetic predisposition and nondisease testing (2002) (9)
- Reliability of polymerase chain reaction (PCR) analysis of single cells for preimplantation genetic diagnosis (1994) (9)
- O-4. Nuclear abnormalities in a series of 6733 human oocytes (2002) (9)
- PGD impact on stem cell transplantation (2009) (9)
- Construction and Sequence Analysis of Subtraction Complementary DNA Libraries from Human Preimplantation Embryos (1999) (9)
- Preimplantation cytogenetic analysis (1992) (9)
- Progress in Preimplantation Genetics (2004) (8)
- An Atlas of Preimplantation Genetic Diagnosis: An Illustrated Textbook & Reference for Clinicians, Second Edition (2004) (8)
- Management of a triplet gestation complicated by uterus didelphys. (1997) (8)
- Clinical Outcome of PGD (2005) (7)
- Preimplantation genetic diagnosis for early-onset torsion dystonia. (2004) (7)
- To PGD or not to PGD: is there a magic number of oocytes to start with? (2007) (7)
- P-10. Optimization of high-resolution single cell comparative genomic hybridization to fit into a PGD framework (2002) (7)
- High Frequency of Meiosis II Aneuploidies in IVF Patients of Advanced Maternal Age (2000) (6)
- Sequence Analysis of Libraries from Individual Human Blastocysts (1998) (6)
- Histomorphological Aspects of Chorionic Villi in First Trimester Fetal Diagnosis (1985) (6)
- Preimplantation Diagnosis: An Alternative to Prenatal Diagnosis of Genetic and Chromosomal Disorders (1999) (6)
- Cytoplasmic cell fusion (2006) (5)
- Evolutionary Classification of Homeodomains (1998) (5)
- Preimplantation diagnosis for long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency. (2001) (5)
- O-139: Preimplantation genetic diagnosis (PGD) for all cystic fibrosis (CF) carrier couples: Strategy and cost analysis (2006) (5)
- Preimplantation HLA (human lymphocyte antigen) testing (2004) (4)
- Isolation of Human Embryonic Stem Cells from Various Stages of the Human Embryo (2009) (4)
- Preimplantation diagnosis of single disorders. (1998) (4)
- Preimplantation FISH diagnosis of aneuploidies. (2002) (4)
- Biopsy of Human Gametes (1991) (4)
- Technical Aspects of Chorionic Villi Sampling in First Trimester Fetal Diagnosis (1985) (4)
- Crown–rump lengths in missed miscarriages and trisomy 21 (2001) (4)
- Accuracy and Outcomes of 3631 Preimplantation Genetic Diagnosis (PGD) Cycles Performed in One Center (2005) (3)
- Polar body preimplantation diagnosis in aging IVF patients (2000) (3)
- P-20. Haploidization of somatic cell nuclei by cytoplasm of human oocytes (2002) (3)
- Techniques for Micromanipulation and Biopsy of Human Gametes and Preembryos (1991) (3)
- Sperm DNA genotyping for preimplantation genetic diagnosis (PGD) (2004) (3)
- O▪57 PGD for aneuploidy or for chromosomal translocation significantly improves assisted reproduction and pregnancy outcome (2005) (2)
- P▪15 Polar body and blastomere analysis for fragile X syndrome with inside gene and flanking VNTR and SNP (2005) (2)
- The future of preimplantation genetic diagnosis (2006) (2)
- O▪53 Developmental potential of embryos after one to three biopsy procedures for PGD (2005) (2)
- LETTERS TO THE EDITOR. AUTHORS REPLY BY Y. VERLINSKY AND C.M. STROM (1996) (2)
- O▪50 No increased birth defects in 576 live born babies after PGD (2005) (2)
- Preimplantation genetic diagnosis and its role in assisted reproduction technology (2005) (2)
- Clinical application of polar body biopsy (2008) (2)
- Ethics of preimplantation genetic diagnosis (2018) (2)
- Preconception diagnosis of single gene and chromosomal disorders. (1994) (2)
- Decreasing risk of pregnancy loss following chorionic villus sampling. Elimination of transabdominal chorionic villus sampling during the ninth week of pregnancy. (1992) (2)
- Successful Selection of Normal Embryos Using PGD in a Woman with Spinocerebellar Ataxia Type 3 (2005) (2)
- Single gene mutations in early embryonic loss (1992) (2)
- Review: Borders, patterns, and distinctive families of homeodomains (1994) (2)
- Elevated maternal serum α-fetoprotein associated with placenta accreta (1992) (1)
- O▪72 Preimplantation diagnosis for β-thalassaemia in Cyprus (2005) (1)
- O-32. Preimplantation non-disease testing (2002) (1)
- Preimplantation genetic diagnosis as a source of human embryonic stem cell lines (2008) (1)
- Clinical outcome of preimplantation genetic diagnosis for chromosome translocations (2004) (1)
- Preimplantation genetic diagnosis for cancer (2002) (1)
- O-14. Preimplantation diagnosis for β-globin gene mutations (2002) (1)
- Developmental potential of embryos after 1 to 3 biopsy procedures for preimplantation genetic diagnosis (PGD) (2004) (1)
- O-47. Clinical outcome following PGD in one large centre (2002) (1)
- The fate of frozen/thawed embryos derived from cycles with preimplantation genetic diagnosis (2004) (1)
- Does ovarian stimulation protocol for IVF and number of oocytes retrieved affect embryos' aneuploidy rate? (2008) (1)
- Reply to Letter to the Editor – Why PGD for aneuploidy should benefit reproductive outcome in poor prognosis IVF patients (2008) (1)
- Investigation of genetic disease-specific human ESC lines: human ESC model of Huntington disease (2009) (0)
- Preembryonic Diagnosis for Genetic Disorders (2000) (0)
- COMMENT ON: CROSS-HYBRIDIZATION OF THE CHROMOSOME 13/21 ALPHA SATELLITE DNA PROBE TO CHROMOSOME 22 IN THE PRENATAL SCREENING OF COMMON ANEUPLOIDIES BY FISH. AUTHORS' REPLY (1996) (0)
- Preimplantation diagnosis for genetic disorders (2010) (0)
- O▪11 PGD with HLA and aneuploidy testing (2005) (0)
- O▪18 Testing for meiosis errors (2005) (0)
- Should preimplantation genetic diagnosis be offered universally (2007) (0)
- Preimplantation Diagnosis for Mendelian Disorders (2009) (0)
- O-30. Nuclear transfer for full karyotyping and PGD for chromosomal translocations (2002) (0)
- Should IVF centers offer preimplantation genetic diagnosis? Yes. (2003) (0)
- Preimplantation Genetic Diagnosis Illustrated (2004) (0)
- Conversion and non-conversion approach to PGD for 474 cases of translocations (2009) (0)
- P-2. Preimplantation diagnosis for early onset Alzheimer disease (2002) (0)
- Cell engineering and genetic approaches to development of human embryonic stem cell models for genetic disorders (2010) (0)
- PGD for familial hemiplegic migraine on polar bodies and blastomeres (2009) (0)
- Review of Current Methods and Experience in Preimplantation Genetic Diagnosis (2004) (0)
- 6 and Future Perspectives of Fetal Genetic Diagnosis (1990) (0)
- P▪13 PGD for Pelizaeus▪Merzbacher disease combined with polymerase chain reaction-based aneuploidy testing for chromosomes 13, 16, 18, 21, 22, X and Y (2005) (0)
- Preimplantation Genetic Diagnosis: Approaches and Current Status (1990) (0)
- Analyses of 95 First-Trimester Chorionic Villus Sampling and Spontaneous Karyotype Abortions by (0)
- P-187. Preimplantation diagnosis using novel techniques (1999) (0)
- 7.002 Preimplantation genetic diagnosis for hypophosphatasia (2008) (0)
- Contents Vol. 111, 2005 (2005) (0)
- Polymerase Chain Reaction と Fluorescent In Situ Hybridization の結合法による着床前性別診断 (1996) (0)
- Scientific program (2007) (0)
- The world's first and largest repository of human ESC lines with genetic and chromosomal disorders (2009) (0)
- Preimplantation cytogenetic analysis. In 'Preimplantation diagnosis of genetic diseases' (1992) (0)
- The Benefits of Preimplantation Genetic Diagnosis for Chromosomal Aneuploidy (2009) (0)
- Potential Impact of PCR-based Aneuploidy Testing on Accuracy and Outcomes of Preimplantation Genetic Diagnosis (PGD) for Mendelian Disorders and HLA Typing (2005) (0)
- Oocyte-like structures arising from cells of follicular fluid are not captured in aspirates. (2009) (0)
- P▪55 Development of preconception testing for paternally derived mutations by sperm duplication (2005) (0)
- Correlation between preimplantation genetic diagnosis results and soluble HLA G concentrations in embryo culture media (2007) (0)
- O▪85 Meiotic outcome based on PGD for 234 cases of translocations (2005) (0)
- O▪7 Expanding indications for PGD (2005) (0)
- Cooperation between the International Working Group on Preimplantation Genetics and Reproductive BioMedicine Online (2002) (0)
- Anglo-Saxon attitudes – an obstacle for development of preimplantation genetic diagnosis in the UK (2002) (0)
- O-3. Present status and impact of PGD: experience in one large centre (2002) (0)
- O-136:Preimplantation genetic diagnosis of chromosome rearrangements by analysis of metaphase spreads obtained after selective embryo biopsy on day 3 (2006) (0)
- Preimplantation genetic diagnosis (PGD) for aneuploidy significantly improves ART and pregnancies outcome (2004) (0)
- Preimplantation genetic diagnosis and therapy (2008) (0)
- O-142. Pregnancy rate following preimplantation testing of polar body aneuploidy in IVF patients of advanced maternal age (1997) (0)
- O▪91 Embryoid body differentiation of human embryonic stem cells maintained in serum-free and feeder-free conditions (2005) (0)
- P▪11 PGD for spinocerebellar ataxia type 2, 3, 6, and 7 (2005) (0)
- Genetic Diagnosis of Metaphase II Oocytes (2004) (0)
- P▪54 Development of conventional blastomere metaphase chromosome analysis for PGD (2005) (0)
- Polar body chromosome abnormalities and their consequences for human embryo development (2007) (0)
- Cytogenetic discrepancies in CVS: genetic counseling issues and dilemmas. (1990) (0)
- O-007 Preimplantation testing for common chromosomal aneuploidies in IVF patients of advanced maternal age (1997) (0)
- Accuracy of preimplantation genetic diagnosis (PGD) of single gene and chromosomal disorders (1994) (0)
- Why PGD for aneuploidy should benefit reproductive outcome in poor prognosis IVF patients (2008) (0)
- DYSMORPHIC SYNDROME, SPHEROCYTOSIS AND PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME 8 (1984) (0)
- O▪56 Obstetrical outcome after preimplantation genetics (2005) (0)
- Preimplantation HLA typing with aneuploidy (2006) (0)
- Does IVF with PGD and blastocyst transfer affect offspring's sex-ratio? (2007) (0)
- Elevated maternal serum alpha-fetoprotein associated with placenta accreta. (1992) (0)
- Application of genetic technology: a genuine step towards improving IVF standards (2008) (0)
- Discussion (day 1 session 2): Designer babies. (2005) (0)
- O▪89 Repository of human embryonic stem cell lines (2005) (0)
- Current and Future Perspectives of Fetal Genetic Diagnosis (1990) (0)
- P▪12 PGD for oculocutaneous albinism type II (2005) (0)
- Nuclear transfer techniques for preimplantation diagnosis and prospect for artificial gamete formation (2004) (0)
- Preimplantation genetic diagnosis for Zellweger syndrome (2008) (0)
- O▪90 Reprogramming of human adult cells by cytoplast of human embryo stem cells (2005) (0)
- The first oocyte donor bank and "Oocyte Donorship" program realization (2000) (0)
- Dizygotic Twins in a Monochorionic Placenta (2001) (0)
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