Dorothy Warburton

Dorothy Warburton's AcademicInfluence.com Rankings

Dorothy Warburton

Biology

#8289

World Rank

#11341

Historical Rank

Genetics

#852

World Rank

#946

Historical Rank

Molecular Biology

#1116

World Rank

#1141

Historical Rank

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Biology

Dorothy Warburton's Degrees

PhD Genetics University of British Columbia

Why Is Dorothy Warburton Influential?

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According to Wikipedia, Dorothy Pamela Warburton was a Canadian geneticist whose research focused on fetal chromosomal abnormalities and reasons for miscarriage. She died at the age of 80 on 26 April 2016 at her home in Englewood, New Jersey.

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Dorothy Warburton'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

Strong Association of De Novo Copy Number Mutations with Autism (2007) (2746)
De novo mutations in histone modifying genes in congenital heart disease (2013) (740)
De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints. (1991) (682)
Location of ribosomal DNA in the human chromosome complement. (1972) (503)
Mapping, cloning and genetic characterization of the region containing the Wilson disease gene (1993) (464)
Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired (1998) (447)
SPONTANEOUS ABORTION RISKS IN MAN: DATA FROM REPRODUCTIVE HISTORIES COLLECTED IN A MEDICAL GENETICS UNIT. (1964) (427)
Molecular definition of 22q11 deletions in 151 velo-cardio-facial syndrome patients. (1997) (360)
Immunolocalization of CENP-A suggests a distinct nucleosome structure at the inner kinetochore plate of active centromeres (1997) (360)
The genetic architecture of Down syndrome phenotypes revealed by high-resolution analysis of human segmental trisomies (2009) (355)
The distribution of chromosomal genotypes associated with Turner's syndrome: livebirth prevalence rates and evidence for diminished fetal mortality and severity in genotypes associated with structural X abnormalities or mosaicism (2004) (271)
DRINKING DURING PREGNANCY AND SPONTANEOUS ABORTION (1980) (246)
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies (2016) (225)
Increased Frequency of De Novo Copy Number Variants in Congenital Heart Disease by Integrative Analysis of Single Nucleotide Polymorphism Array and Exome Sequence Data (2014) (197)
Catalogue of unbalanced chromosome aberrations in man (2004) (173)
Does the karyotype of a spontaneous abortion predict the karyotype of a subsequent abortion? Evidence from 273 women with two karyotyped spontaneous abortions. (1987) (170)
Identification of a novel member of the TGF-beta superfamily highly expressed in human placenta. (1997) (167)
Smoking: A Risk Factor for Spontaneous Abortion (1977) (165)
Turner syndrome revisited: review of new data supports the hypothesis that all viable 45,X cases are cryptic mosaics with a rescue cell line, implying an origin by mitotic loss (2014) (161)
The 13q- syndrome: the molecular definition of a critical deletion region in band 13q32. (1995) (159)
Trisomy recurrence: a reconsideration based on North American data. (2004) (158)
Preliminary definition of a "critical region" of chromosome 13 in q32: report of 14 cases with 13q deletions and review of the literature. (1993) (155)
Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors. (1997) (155)
Cutaneous T-cell lymphoma: neoplasm of T cells with helper activity. (1979) (140)
Associations between both genetic and environmental biomarkers and lung cancer: evidence of a greater risk of lung cancer in women smokers. (1998) (133)
Chromosomal non-disjunction in human oocytes: is there a mitochondrial connection? (2000) (127)
Proposed guidelines for diagnosis of chromosome mosaicism in amniocytes based on data derived from chromosome mosaicism and pseudomosaicism studies (1992) (126)
Association of stressful life events with chromosomally normal spontaneous abortion. (1996) (119)
The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease (2013) (114)
CYTOGENETIC ABNORMALITIES IN SPONTANEOUS ABORTIONS OF RECOGNIZED CONCEPTIONS (1986) (113)
Trisomic pregnancy and earlier age at menopause. (2000) (111)
Morphology of early fetal deaths and their chromosomal characteristics. (1985) (110)
Increased rate of aneuploid embryos in young women with previous aneuploid conceptions (2004) (109)
The 13q-deletion syndrome. (1969) (108)
Biological aging and the etiology of aneuploidy (2005) (106)
Chromosomal Aberrations in Cord Blood Are Associated with Prenatal Exposure to Carcinogenic Polycyclic Aromatic Hydrocarbons (2005) (104)
Ribosomal DNA Connectives between Human Acrocentric Chromosomes (1973) (102)
Variation in the number of genes for rRNA among human acrocentric chromosomes: correlation with frequency of satellite association. (1976) (97)
Molecular cytogenetic analysis of eight inversion duplications of human chromosome 13q that each contain a neocentromere. (2000) (96)
The effect of maternal age on the frequency of trisomy: change in meiosis or in utero selection? (1989) (96)
Spontaneous abortion as a screening device. The effect of fetal survival on the incidence of birth defects. (1975) (94)
Sequential silver staining and hybridization in situ on nucleolus organizing regions in human cells. (1979) (90)
Cell type-specific over-expression of chromosome 21 genes in fibroblasts and fetal hearts with trisomy 21 (2006) (90)
Effect of maternal age on autosomal trisomies (1980) (87)
Mosaic tetrasomy 12p: four new cases, and confirmation of the chromosomal origin of the supernumerary chromosome in one of the original Pallister-Mosaic syndrome cases. (1987) (85)
The cri du chat syndrome in adolescents and adults: clinical finding in 13 older patients with partial deletion of the short arm of chromosome No. 5(5p-). (1970) (83)
Molecular and genetic damage from environmental tobacco smoke in young children. (1999) (83)
Increased expression of cyclin D1 and the Rb tumor suppressor gene in c-K-ras transformed rat enterocytes. (1996) (82)
Chromosome anomalies and prenatal development : an atlas (1991) (79)
Multiplex interphase FISH as a screen for common aneuploidies in spontaneous abortions. (2002) (78)
A microsatellite genetic linkage map of human chromosome 13. (1993) (77)
Karyotype studies of cutaneous T cell lymphoma: evidence for clonal origin. (1979) (77)
The relationship of maternal age and trisomy among trisomic spontaneous abortions. (1984) (77)
MONOSOMY X: A CHROMOSOMAL ANOMALY ASSOCIATED WITH YOUNG MATERNAL AGE (1980) (77)
Outcome of cases of de novo structural rearrangements diagnosed at amniocentesis (1984) (75)
Chromosome structure as revealed by a combined chemical and immunochemical procedure. (1973) (75)
The significance of cystic hygroma in fetuses. (1984) (74)
Demonstration of the genuine iso-12p character of the standard marker chromosome of testicular germ cell tumors and identification of further chromosome 12 aberrations by competitive in situ hybridization. (1991) (70)
Report of the committee on comparative mapping. (1980) (70)
Mosaic autosomal trisomy in cultures from spontaneous abortions. (1978) (70)
The relationship between maternal age and chromosome size in autosomal trisomy. (1986) (69)
Consistent pattern of binding of anti-adenosine antibodies to human metaphase chromosomes. (1972) (68)
Diagnosis of cutaneous T cell lymphoma by use of monoclonal antibodies reactive with tumor-associated antigens. (1982) (68)
Monochromosomal rodent-human hybrids from microcell fusion of human lymphoblastoid cells containing an inserted dominant selectable marker. (1990) (68)
Cigarette smoking and spontaneous abortion of known karyotype. Precise data but uncertain inferences. (1995) (66)
Fever during pregnancy and spontaneous abortion. (1985) (66)
Neural tube defects in spontaneous abortions. (1986) (66)
Biologic markers in ethylene oxide-exposed workers and controls. (1991) (66)
Male excess among anatomically normal fetuses in spontaneous abortions. (1987) (64)
Translocation heterozygosis: a cause of five cases of the cri du chat syndrome and two cases with a duplication of chromosome number five in three families. (1967) (64)
Biomarkers in styrene-exposed boatbuilders. (1991) (63)
Polycyclic aromatic hydrocarbon-DNA adducts in spontaneously aborted fetal tissue. (1990) (62)
Construction of a yeast artificial chromosome contig spanning the spinal muscular atrophy disease gene region. (1993) (61)
Preferential X-chromosome activity in human female placental tissues. (1986) (59)
Chromosomal differences in susceptibility to meiotic aneuploidy (1996) (59)
A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice. (2008) (58)
A stable human dicentric chromosome, t dic (12;14)(p13;p13) including an intercalary satellite region between centromeres. (1973) (57)
Congenital Cleft Lip and Palate: Risk Figures for Counseling (1961) (57)
Smoking: a risk factor for spontaneous abortion. (1978) (56)
NO ASSOCIATION OF EMOTIONAL STRESS OR VITAMIN SUPPLEMENT DURING PREGNANCY TO CLEFT LIP OR PALATE IN MAN (1964) (55)
DNA adducts and related biomarkers in populations exposed to environmental carcinogens (1992) (54)
Maternal age and spontaneous abortion (1980) (54)
Structural Chromosomal Rearrangements Require Nucleotide-Level Resolution: Lessons from Next-Generation Sequencing in Prenatal Diagnosis. (2016) (54)
Surveillance of spontaneous abortions. Power in environmental monitoring. (1977) (53)
Detection of Chromosomal Aberrations in Clinical Practice: From Karyotype to Genome Sequence. (2015) (52)
Partial deletion of the short arm of chromosome no. 4(4p-): clinical studies in five unrelated patients. (1970) (51)
Maternal smoking and trisomy among spontaneously aborted conceptions. (1983) (51)
Isolation and characterization of a highly malignant variant of the SW480 human colon cancer cell line. (1992) (51)
THE GENETICS OF INCONTINENTIA PIGMENTI. (1965) (50)
A de novo mutation (Gln2Stop) at the 5' end of the SRY gene leads to sex reversal with partial ovarian function. (1998) (49)
Multiple biological markers in germ cell tumor patients treated with platinum-based chemotherapy. (1992) (49)
Chromosome analysis of two related heteroploid mouse cell lines by quinacrine fluorescence. (1973) (47)
Acute myeloid leukemia as the first hematologic manifestation of fanconi anemia (1982) (46)
CAFFEINE AND SPONTANEOUS ABORTION OF KNOWN KARYOTYPE (1991) (46)
Trisomic pregnancy and the oocyte pool. (2004) (46)
ON THE PROBABILITY THAT A WOMAN WHO HAS HAD A SPONTANEOUS ABORTION WILL ABORT IN SUBSEQUENT PREGNANCIES (1961) (45)
Amniotic band syndrome associated with amniocentesis. (1981) (44)
Alternative DNA replication patterns associated with long arm length of chromosomes 4 and 5 in the cri du chat syndrome. (1966) (41)
Preliminary communication: prenatal detection of the Fanconi Anemia gene by cytogenetic methods. (1979) (41)
Cytogenetic methods for the mouse: preparation of chromosomes, karyotyping, and in situ hybridization. (1990) (40)
Position effect on FGF13 associated with X-linked congenital generalized hypertrichosis (2013) (40)
Mutations in the Cholesterol Transporter Gene ABCA5 Are Associated with Excessive Hair Overgrowth (2014) (39)
Caveat to genotype–phenotype correlation in mucopolysaccharidosis type II: Discordant clinical severity of R468W and R468Q mutations of the iduronate‐2‐sulfatase gene (1993) (39)
Uniparental disomy: a rare consequence of the high rate of aneuploidy in human gametes. (1988) (38)
Human female meiosis: new insights into an error-prone process. (1997) (38)
Characteristics of women with recurrent spontaneous abortions and women with favorable reproductive histories. (1986) (37)
Report of the committee on comparative mapping. (1979) (37)
Application of ROMA (representational oligonucleotide microarray analysis) to patients with cytogenetic rearrangements (2005) (36)
Clonal chromosomal abnormalities in cutaneous T-cell lymphoma. (1987) (36)
Dual genotype in cutaneous T cell lymphoma: immunoglobulin gene rearrangement in clonal T cell malignancy. (1988) (35)
A test for Fanconi's anemia. (1987) (35)
Trisomic pregnancy and elevated FSH: implications for the oocyte pool hypothesis. (2011) (34)
Morphological characteristics of monosomy X in spontaneous abortions. (1988) (34)
GENETIC ASPECTS OF ABORTION (1959) (34)
Distinction between chromosome 4 and chromosome 5 by replication pattern and length of long and short arms. (1967) (33)
Partial dystrophin deficiency in monozygous twin carriers of the Duchenne gene discordant for clinical myopathy (1990) (31)
Validation of QF‐PCR for prenatal aneuploidy screening in the United States (2006) (31)
Identification and expression analysis of the human mu-protocadherin gene in fetal and adult kidneys. (2002) (30)
Dystonia in a patient with deletion of 18q (1995) (30)
Localization of rDNA and giemsa-banded chromosome complement of white-handed gibbon, Hylobates lar (2004) (30)
Cigarette smoking and trisomy 21 at amniocentesis (1993) (29)
Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole‐genome sequencing (2015) (29)
Regulation of rRNA gene expression in a human familial 14p+ marker chromosome (1978) (28)
Mosaic variegated aneuploidy with microcephaly: a new human mitotic mutant? (1991) (28)
Dermatoglyphic features of patients with a partial short arm deletion of a B‐group chromosome (1967) (27)
The value of chromosome analysis in cases of neural tube defects: A case of anencephaly associated with fetal DUP(2) (p24→pter) (1987) (27)
The chromosomal location of rDNA in selected lower primates. (1977) (27)
DE NOVO STRUCTURAL REARRANGEMENTS: IMPLICATIONS FOR PRENATAL DIAGNOSIS (1982) (27)
Selection of cDNAs using chromosome-specific genomic clones: application to human chromosome 13. (1994) (27)
Improved methods of direct and cultured chromosome preparations from chorionic villous samples. (1986) (27)
Primary hypogonadism and 13/15 chromosome translocation in Prader-Labhart-Willi syndrome. (1981) (27)
Genetic factors influencing aneuploidy frequency. (1985) (26)
Two reciprocal translocations associated with microcephaly and retardation. (1977) (26)
High-resolution YAC-cosmid-STS map of human chromosome 13. (1998) (26)
Reproductive loss: how much is preventable? (1987) (26)
Cloning of the breakpoints of a de novo inversion of chromosome 8, inv (8)(p11.2q23.1) in a patient with Ambras syndrome (2004) (26)
Complex cytogenetic rearrangement of chromosome 8q in a case of Ambras syndrome. (2001) (26)
Induced abortion and the chromosomal characteristics of subsequent miscarriages (spontaneous abortions). (1986) (25)
A "Philadelphia-like" chromosome derived from the Y in a patient with refractory dysplastic anemia. (1973) (25)
Interstitial translocation in man. (1972) (25)
Paternal age and trisomy among spontaneous abortions (1990) (25)
Renal oncocytomas with rearrangements involving 11q13 contain breakpoints near CCND1. (2004) (24)
Using FISH to increase the yield and accuracy of karyotypes from spontaneous abortion specimens (2011) (24)
Epidemiologic detection of low dose effects on the developing fetus. (1981) (24)
Application of new staining techniques to the study of human chromosomes. (1973) (24)
Clusterine in deleted short-arm length among 25 cases with a Bp-chromosome. (1969) (23)
Giemsa banding of chromosomes. (1972) (22)
Pericentric inversion of the Y chromosome and prenatal diagnosis (1984) (22)
Induced abortion and spontaneous abortion: no connection? (1978) (22)
Skewed X chromosome inactivation and trisomic spontaneous abortion: no association. (2009) (22)
Localization of rDNA in the chromosome complement of the Rhesus (Macaca mulatta) (1974) (22)
Genomic cloning and chromosomal assignment of the E2F dimerization partner TFDP gene family. (1997) (22)
Association of schizophrenia and partial trisomy of chromosome 5p A case report (1992) (20)
Genetic mapping of soluble guanylyl cyclase genes: implications for linkage to blood pressure in the Dahl rat. (1998) (20)
Assignment of GUCIA2, the gene coding for the alpha 2 subunit of soluble guanylyl cyclase, to position 11q21-q22 on human chromosome 11. (1996) (20)
Prenatal PAH exposure is associated with chromosome-specific aberrations in cord blood. (2010) (20)
Lack of association between spermicide use and trisomy. (1987) (20)
Vaginal spermicides and spontaneous abortion of known karyotype. (1986) (20)
Chromosomal distribution of rDNA in Pan paniscus, Gorilla gorilla beringei, and Symphalangus syndactylus: Comparison to related primates (1976) (20)
Recurrent spontaneous abortion: Definition of a syndrome (1980) (19)
Genetic Mapping of Soluble Guanylyl Cyclase Genes Implications for Linkage to Blood Pressure in the Dahl Rat (1998) (19)
In utero selection against fetuses with trisomy. (1983) (19)
Detection of variant Ph-positive chronic myelogenous leukemia involving chromosomes 1, 9, and 22 by fluorescence in situ hybridization. (1993) (19)
Urinary Naphthol Metabolites and Chromosomal Aberrations in 5-Year-Old Children (2012) (19)
Cloning and characterization of DIP1, a novel protein that is related to the Id family of proteins. (2000) (19)
Congenital universal hypertrichosis with deafness and dental anomalies inherited as an X‐linked trait (2003) (18)
Autoradiographic studies on a mother and aborted foetus from a family with four mongoloid children and a presumptive 21/21 translocation (1968) (18)
Location ofRibosomal DNA intheHumanChromosome Complement (1972) (17)
p82H identifies sequences at every human centromere (1987) (17)
TRISOMY CLUSTER IN NEW YORK (1977) (17)
A single gene for human TRAF-3 at chromosome 14q32.3 encodes a variety of mRNA species by alternative polyadenylation, mRNA splicing and transcription initiation. (1998) (17)
A fetus with a chromosome 13 ring and placenta with chromosome 13 rod/ring mosaicism (1983) (17)
Hypoplastic left heart in a female infant with partial trisomy 4q due to de novo 4;21 translocation. (2002) (16)
Spontaneous abortion and the use of sugar substitutes (saccharin). (1978) (16)
Memory in myasthenia gravis (1996) (15)
Maternal employment and the chromosomal characteristics of spontaneously aborted conceptions. (1985) (15)
Kearns‐Sayre syndrome in twins (1988) (15)
Marijuana and spontaneous abortion of known karyotype. (1991) (15)
Spermicide use and pregnancy outcome. (1988) (15)
The proximal chromosome 14q microdeletion syndrome: Delineation of the phenotype using high resolution SNP oligonucleotide microarray analysis (SOMA) and review of the literature (2011) (15)
Intermediate CGG repeat length at the FMR1 locus is not associated with hormonal indicators of ovarian age (2014) (15)
Fingerprint arches in alopecia areata. (1974) (14)
A new allele of Gli3 and a new mutation, circletail (Crc), resulting from a single transgenic experiment (2002) (14)
Detection of minute deletions in human karyotypes. (1969) (14)
A high-resolution annotated physical map of the human chromosome 13q12-13 region containing the breast cancer susceptibility locus BRCA2. (1996) (14)
Fluorescence in situ hybridization is necessary to detect an association between chromosome aberrations and polycyclic aromatic hydrocarbon exposure in utero and reveals nonrandom chromosome involvement (2007) (13)
Localization of rDNA in the chimpanzee (Pan troglodytes) chromosome complement (2004) (13)
Some pathologic findings in spontaneous abortions. (1979) (12)
Assembly of ordered contigs of cosmids selected with YACs of human chromosome 13. (1994) (12)
A 9/11 translocation in a child with Ph1-negative chronic myelogenous leukemia. (1976) (12)
The site of 5S RNA genes in primates (1976) (12)
Retinoblastoma and partial deletion of the long arm of chromosome 13. (1978) (12)
PITFALLS IN TESTS FOR TERATOGENICITY (1962) (11)
Gonadal dysgenesis in association with autosomal chromosome aberration. (1978) (11)
Prenatal diagnosis of sickle hemoglobinopathies: the experience of the Columbia University Comprehensive Center for Sickle Cell Disease. (1987) (11)
A unique case of der(11)t(11;22),‐22 arising from 3:1 segregation of a maternal t(11;22) in a family with co‐segregation of the translocation and breast cancer (2005) (11)
Distal duplication 14q: Report of three cases and further delineation of the syndrome (2004) (10)
Genetic and epidemiologic investigation of spontaneous abortion: relevance to clinical practice. (1979) (10)
Absence of somatic pairing of sex chromatin masses (inactivated X chromosomes) in cultured cells from a human XXXXY male. (1967) (9)
Duplication of the ZIC2 gene is not associated with holoprosencephaly (2012) (9)
Report of the Third International Workshop on Human Chromosome 13 Mapping 1995 (1996) (9)
X-chromosome inactivation and ovarian age during the reproductive years. (2006) (9)
Risk of phenotypic abnormalities in paracentric inversion carriers. (1997) (8)
Mutagenesis assays of human amniotic fluid. (1985) (8)
Homogeneously staining region in anthracycline-resistant HL-60/AR cells not associated with MDR1 amplification. (1992) (8)
Studies of Dermatoglyphics in Psoriasis (1968) (8)
Regional localization of 32 NotI-HindIII fragments from a human chromosome 13 library by a somatic cell hybrid panel and in situ hybridization. (1993) (8)
Assignment of cyclophilin A (PPIA) to human chromosome band 7p13by in situ hybridization. (1996) (8)
Alzheimer's disease in the parents of women with trisomic spontaneous abortions (2000) (7)
Trisomy 7 mosaicism: prognosis after prenatal diagnosis (2002) (7)
Neoplastic human T-cells capable of responding to multiple human alloantigens. (1980) (7)
Preparation and Culture of Products of Conception and Other Solid Tissues for Chromosome Analysis (2009) (7)
Copy Number Changes on the X Chromosome in Women with and without Highly Skewed X-Chromosome Inactivation (2012) (7)
The chromosomal location of rDNA in the Sumatran orangutan, Pongo pygmaeus albei. (1979) (7)
Abstracts of meeting presentations (Part 5 of 11) (1979) (6)
The control of sex chromatin (1968) (6)
The control of sex chromatin. I. The significance of the distribution of sex chromatin counts in individuals with three or more X chromosomes. (1968) (6)
Letter: Ribosomal DNA connectives between human acrocentric chromosomes. (1973) (6)
Genomic changes in glioblastoma cell lines detected by comparative genomic hybridization (2004) (6)
Trisomic pregnancy and intermediate CGG repeat length at the FMR1 locus. (2012) (6)
2006 William Allan Award Address. Having it all. (2007) (6)
The location of RN5S genes on the chromosomes of primates. (1976) (6)
Evidence for smaller probabilities for trisomic mosaicism for acrocentric than for nonacrocentric chromosomes. (1981) (5)
Autoradiographic studies of chromosomes 4 and 5 in the cri du chat syndrome (1965) (5)
Epidemiologic Studies of Enviromental Exposures in Human Reproduction (1981) (5)
Changes in an inherited ring (22) due to meiotic recombination? Implications for genetic counseling (2009) (5)
Abstracts of meeting presentations (Part 2 of 5) (1979) (5)
Trisomy clusters in New York. (1977) (5)
Current techniques in chromosome analysis. (1980) (5)
Prenatal diagnosis of a familial Xq deletion in a female fetus: a case report (2001) (5)
The role of trypsin in the pre-treatment of chromosomes for giemsa banding (1976) (5)
Abstracts of meeting presentations (Part 3 of 11) (1979) (4)
The biarmed Mus poschiavinus chromosome carrying the H-2 locus, T1posKlj, IS T7Bnr. (1972) (4)
Scrambling Eggs in Plastic Bottles (2007) (4)
Identification and characterization of three genes and two pseudogenes on chromosome 13 (1996) (3)
Biological Monitoring of Exposure to Polycyclic Aromatic Hydrocarbons (1991) (3)
Present Status and Future Trends in Prenatal Diagnosis of Chromosomal Disorders (1972) (3)
No maternal age relationship for polyploidy (1994) (3)
Partial uniparental disomy with mosaic deletion 13q in an infant with multiple congenital anomalies (2013) (2)
Workshop on collaborative studies in prenatal diagnosis of chromosome disease. (1982) (2)
Congenital Cleft Lip and Palate (2016) (2)
Heteroploidy in IUD-associated pregnancy. (1979) (2)
Risk of Down's syndrome. (1970) (2)
Computer-assisted analysis of data from hybridization in situ. (1978) (2)
Molecular definition of 22q11 deletions in 151 VCFS patients: integration within a 10kb physical map (1997) (2)
Isolation and Characterization of a Highly Malignant Variant of the SW 480 Human Colon Cancer Cell Line (2007) (2)
Preparation and culture of products of conception and other solid tissues for chromosome analysis. (2001) (2)
In recent years, computer technology has seen advances which have had a major impact on the practice of medicine. (2000) (1)
Screening for Hemoglobinopathies in New York City (1988) (1)
Fishing for new genes in skin biology: impact of cytogenetics on gene discovery (2004) (1)
Genetics of obstetrical variables. A study from the collaborative perinatal project * (1974) (1)
Fetal tissue supply. (1992) (1)
Effects of common environmental exposures on spontaneous abortion of defined karyotype. (1985) (1)
Comparative genomic hybridization: FISH and chips in our future? (1999) (1)
Erratum/correction for Bocskay et al. 2007 Environ Mol Mutagen 48(2):114–123 (2007) (1)
The contribution of de novo and rare inherited copy number changes to congenital heart disease in an unselected sample of children with conotruncal defects or hypoplastic left heart disease (2013) (1)
Molecular and Genetic Damage from Environmental Tobacco Smoke in Young Children 1 (1999) (1)
Duration of vaginal bleeding and trisomy at prenatal diagnosis (1987) (1)
Introductory Speech for F. Clarke Fraser (2001) (1)
Deleted late-replicating chromosomes. (1966) (0)
The genetics of incontinentia pigmenti. (1965) (0)
Catalog of mapped human gene markers. (1980) (0)
UrinaryNaphthol Metabolites andChromosomal Aberrations in 5-Year-Old Children (2012) (0)
alloantigens Neoplastic human T-cells capable of responding to multiple human (2011) (0)
The location of RN5S genes on the chromosomes of primates. (1976) (0)
Subject Index Vol. 25, 1979 (1979) (0)
Editorial help (2004) (0)
Turner syndrome revisited: review of new data supports the hypothesis that all viable 45,X cases are cryptic mosaics with a rescue cell line, implying an origin by mitotic loss (2014) (0)
Chromosome Analysis and Identification (2006) (0)
Subject Index Vol. 16, 1976 (1976) (0)
Dermatoglyphic features of patients with a partial short arm deletion of a B‐group chromosome* (1967) (0)
REGIONAL AND LOCAL SOCIETIES OF PLASTIC AND RECONSTRUCTIVE SURGERY. (1964) (0)
Prenatal exposures and childhood cancer. (2006) (0)
Abstract B32: Levels of metabolites of naphthalene in urine predict translocations in peripheral blood lymphocytes in children (2010) (0)
Book Review Index Vol. 12, 1973 (1973) (0)
Effects of postconception spermicide use. Response from Dr. Strobino et al. [letter] (1988) (0)
DNAAdducts andRelated Biomarkers in Populations Exposed toEnvironmental (1992) (0)
Fetal loss and caffeine intake. (1994) (0)
Electronic karyotype transmission (2000) (0)
Subject Index, Vol. 74, 1996 (1996) (0)
Response from Dr. Strobino, et al (1988) (0)
DeNovoBalanced ChromosomeRearrangements andExtra MarkerChromosomesIdentified atPrenatal Diagnosis: Clinical Significance andDistribution ofBreakpoints (1991) (0)
renatal PAH exposure is associated with chromosome-specific berrations in cord blood anuela (2010) (0)
To the Editor (2000) (0)
Refractory Dysplastic Anemia A "Philadelphia-like" Chromosome Derived From the Y in a Patient With (2011) (0)
Abstract LB-402: Chromosomal aberrations in 5-year olds and urinary PAH metabolites (2010) (0)
Brief A Stable Human Dicentric Chromosome, t dic (12;14)(pl3;pl3) including an Intercalary Satellite Region between Centromeres (2006) (0)
Addendum to Abstracts of the12th European Colloquium on Cytogenetics of Domestic Animals (1996) (0)
Identification by FISH of 21q22 duplication in patient with Down syndrome and apparent 46,XX karyotype (1994) (0)
888 ACUTE MYELOMONOCYTIC LEUKEMIA AS THE FIRST HEMATOLOGIC MANIFESTATION IN A PATIENT WITH FANCONI ANEMIA (1981) (0)
Index of Volume 28 (2007) (2007) (0)
Subject Index Vol. 22, 1978 (1978) (0)
Cri du chat in older patients: Five cases two of which are familial (1965) (0)
Partial deletion o/the short arm of chromosome No 4(4t,-). Clinical ,t,di , i, unrelated patients (1970) (0)
Do numerical polymorphisms exist at the human 5 S locus? (2004) (0)
Urinary NaphtholMetabolites andChromosomal Aberrations in 5-Year-Old Children (2012) (0)

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