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Fetal Cystic Hygroma: Cause and Natural History

The New England journal of medicine, 1983-10, Vol.309 (14), p.822-825

1983

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CHROMOSOME ANALYSIS OF HUMAN AMNIOTIC-FLUID CELLS

The Lancet (British edition), 1966-01, Vol.287 (7434), p.383-385

1966

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Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype

Nature genetics, 1994-11, Vol.8 (3), p.243-250

1994

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Regional location of α1-antichymotrypsin and α1-antitrypsin genes on human chromosome 14

Somatic cell and molecular genetics, 1986-03, Vol.12 (2), p.209-214

1986

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Oocyte production in a turner syndrome patient with serologically detectable male antigen

Journal of reproductive immunology, 1984, Vol.6 (1), p.19-24

1984

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Regulation of rRNA gene expression in a human familial 14p+ marker chromosome

Human genetics, 1978-01, Vol.43 (3), p.289-297

1978

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An activity program in alcohol education

Health education (Washington, D.C. 1975), 1985-04, Vol.16 (2), p.32

Breg, W R

1985

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21 Monosomy in a retarded female infant

Journal of medical genetics, 1974-12, Vol.11 (4), p.386-389

1974

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Presence of H-Y Antigen in Patients with Ullrich-Turner Syndrome and X-Chromosome Rearrangements

Obstetrical & gynecological survey, 1982-08, Vol.37 (8), p.537-538

1982

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Craniorachischisis in a Partially Trisomic 11 Fetus in a family with Reproductive Failure and a Reciprocal Translocation, t(6p+;11q−)

Journal of medical genetics, 1974-03, Vol.11 (1), p.69-75

1974

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XY Gonadal Dysgenesis Associated with the Congenital Nephrotic Syndrome

Obstetrics and gynecology (New York. 1953), 1980-03, Vol.55 (3 Suppl), p.66S-69S

1980

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Analysis of Human Y-Chromosome-Specific Reiterated DNA in Chromosome Variants

Proceedings of the National Academy of Sciences - PNAS, 1977-03, Vol.74 (3), p.1245-1249

1977

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A comparison of language characteristics of mentally retarded adults with fragile X syndrome and those with nonspecific mental retardation and autism

Journal of autism and developmental disorders, 1987-12, Vol.17 (4), p.457-468

1987

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FAMILY COUNSELING IN DOWNS SYNDROME

Annals of the New York Academy of Sciences, 1970-09, Vol.171 (2), p.645-654

Breg, W. Roy

1970

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Molecular and cytogenetic characterization of 9p- abnormalities

American journal of medical genetics, 1993-05, Vol.46 (3), p.288-292

1993

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Diagnosis of Angelman syndrome in infants

American journal of medical genetics, 1991-01, Vol.38 (1), p.58-64

1991

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Anthropometric and craniofacial patterns in mentally retarded males with emphasis on the fragile X syndrome

Clinical genetics, 1993-09, Vol.44 (3), p.129-138

1993

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Human c-fos Oncogene Mapped within Chromosomal Region 14q21 → q31

Proceedings of the National Academy of Sciences - PNAS, 1984-09, Vol.81 (18), p.5826-5830

1984

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PRENATAL DETECTION OF TWO DIFFERENT MONOSOMIC CELL LINES BY CHORIONIC VILLUS SAMPLING

Prenatal diagnosis, 1996-02, Vol.16 (2), p.169-172

1996

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Summary of the 1993 ASHG ancillary meeting "recent research on chromosome 4p syndromes and genes"

American journal of medical genetics, 1995-02, Vol.55 (4), p.453-458

1995

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Fetal blood sampling and cytogenetic abnormalities

Prenatal diagnosis, 1993-01, Vol.13 (1), p.1-8

1993

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Familial occurrence of esophageal atresia with and without tracheoesophagel fistula:Report of two unusual kindreds

American journal of medical genetics, 1991-06, Vol.39 (4), p.380-384

1991

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Anthropometric comparison of mentally retarded males with and without the fragile X syndrome

American journal of medical genetics, 1991-02, Vol.38 (2-3), p.260-268

1991

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Evidence for methylation of inactive human rRNA genes in amplified regions

Human genetics, 1981-02, Vol.56 (3), p.315-320

1981

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"Pseudomosaicism" for 4p - in amniotic fluid cell culture proven to be true mosaicism after birth

American journal of medical genetics, 1991-04, Vol.39 (1), p.81-83

1991

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Fetal Cystic Hygroma: Cause and Natural History

CHROMOSOME ANALYSIS OF HUMAN AMNIOTIC-FLUID CELLS

Xq-Yq interchange resulting in supernormal X-linked gene expression in severely retarded males with 46,XYq- karyotype

Regional location of α1-antichymotrypsin and α1-antitrypsin genes on human chromosome 14

Oocyte production in a turner syndrome patient with serologically detectable male antigen

Regulation of rRNA gene expression in a human familial 14p+ marker chromosome

An activity program in alcohol education

21 Monosomy in a retarded female infant

Presence of H-Y Antigen in Patients with Ullrich-Turner Syndrome and X-Chromosome Rearrangements

Craniorachischisis in a Partially Trisomic 11 Fetus in a family with Reproductive Failure and a Reciprocal Translocation, t(6p+;11q−)

XY Gonadal Dysgenesis Associated with the Congenital Nephrotic Syndrome

Analysis of Human Y-Chromosome-Specific Reiterated DNA in Chromosome Variants

A comparison of language characteristics of mentally retarded adults with fragile X syndrome and those with nonspecific mental retardation and autism

FAMILY COUNSELING IN DOWNS SYNDROME

Molecular and cytogenetic characterization of 9p- abnormalities

Diagnosis of Angelman syndrome in infants

Anthropometric and craniofacial patterns in mentally retarded males with emphasis on the fragile X syndrome

Human c-fos Oncogene Mapped within Chromosomal Region 14q21 → q31

PRENATAL DETECTION OF TWO DIFFERENT MONOSOMIC CELL LINES BY CHORIONIC VILLUS SAMPLING

Summary of the 1993 ASHG ancillary meeting "recent research on chromosome 4p syndromes and genes"

Fetal blood sampling and cytogenetic abnormalities

Familial occurrence of esophageal atresia with and without tracheoesophagel fistula:Report of two unusual kindreds

Anthropometric comparison of mentally retarded males with and without the fragile X syndrome

Evidence for methylation of inactive human rRNA genes in amplified regions

"Pseudomosaicism" for 4p - in amniotic fluid cell culture proven to be true mosaicism after birth

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