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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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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

Volltextzugriff (PDF)

Fetal cystic hygroma. Cause and natural history

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

1983

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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

Volltextzugriff (PDF)

Deletion (12)(q15q21.2)

Journal of medical genetics, 1989-05, Vol.26 (5), p.343-344

1989

Volltextzugriff (PDF)

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

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

1996

Volltextzugriff (PDF)

Fetal blood sampling and cytogenetic abnormalities

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

1993

Volltextzugriff (PDF)

CHROMOSOME ANALYSIS OF HUMAN AMNIOTIC-FLUID CELLS

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

1966

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Fragile X in a survey of 75 autistic males

The New England journal of medicine, 1984-05, Vol.310 (22), p.1462

1984

Volltextzugriff (PDF)

NRAS transforming gene maps to region p11----p13 on chromosome 1 by in situ hybridization

Cytogenetics and cell genetics, 1984, Vol.38 (1), p.70

1984

Volltextzugriff (PDF)

Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15

Human genetics, 1977-01, Vol.36 (1), p.1-12

1977

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Homogeneously staining region in a retinoblastoma cell line: relevance to tumor initiation and progression

JNCI : Journal of the National Cancer Institute, 1981-08, Vol.67 (2), p.301-306

1981

Volltextzugriff (PDF)

Maternal metaphases on direct chromosome preparation of first trimester decidua

Human genetics, 1985-01, Vol.69 (4), p.380-380

1985

Volltextzugriff (PDF)

Human Thymidine Kinase Gene Locus: Assignment to Chromosome 17 in a Hybrid of Man and Mouse Cells

Science (American Association for the Advancement of Science), 1971-07, Vol.173 (3993), p.244-245

1971

Volltextzugriff (PDF)

An anonymous single copy X-chromosome clone, DXS79, from Xq26-Xq28, identifies a moderately frequent RFLP [HGM8 provisional no. DXS79]

Nucleic acids research, 1985-04, Vol.13 (8), p.3015-3015

1985

Volltextzugriff (PDF)

Molecular and cytogenetic characterization of 9p- abnormalities

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

1993

Volltextzugriff (PDF)

A method of processing first-trimester chorionic villous biopsies for cytogenetic analysis

American journal of human genetics, 1984-11, Vol.36 (6), p.1386-1393

1984

Volltextzugriff (PDF)

Chromosome 3 duplication q/deletion p syndrome

Pediatrics (Evanston), 1978-04, Vol.61 (4), p.611

1978

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Quinacrine Fluorescence for Identifying Metaphase Chromosomes, with Special Reference to Photomicrography

Biotechnic & histochemistry, 1972-01, Vol.47 (2), p.87-93

Breg, W. R.

1972

Volltextzugriff (PDF)

FISH diagnosis of partial trisomy 13 and tetrasomy 13 in a patient with severe trigonocephaly (C) phenotype

American journal of medical genetics, 1994-08, Vol.52 (1), p.92-96

1994

Volltextzugriff (PDF)

Trisomy 8 mosaicism syndrome

Pediatrics (Evanston), 1975-11, Vol.56 (5), p.762

1975

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Complete and partial trisomy of different segments of chromosome 8: case reports and review

Clinical genetics, 1979-12, Vol.16 (6), p.390-398

1979

Volltextzugriff (PDF)

H-Y antigen negative patients with testicular tissue and 46,XY karyotype

Human genetics, 1981-01, Vol.57 (3), p.265-268

1981

Volltextzugriff (PDF)

Quinacrine Fluorescence Patterns of Human D Group Chromosomes

Nature (London), 1971-07, Vol.232 (5305), p.24-27

1971

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

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

Fetal cystic hygroma. Cause and natural history

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

Deletion (12)(q15q21.2)

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

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

Fetal blood sampling and cytogenetic abnormalities

CHROMOSOME ANALYSIS OF HUMAN AMNIOTIC-FLUID CELLS

Fragile X in a survey of 75 autistic males

NRAS transforming gene maps to region p11----p13 on chromosome 1 by in situ hybridization

Preferential derivation of abnormal human G-group-like chromosomes from chromosome 15

Homogeneously staining region in a retinoblastoma cell line: relevance to tumor initiation and progression

Maternal metaphases on direct chromosome preparation of first trimester decidua

Human Thymidine Kinase Gene Locus: Assignment to Chromosome 17 in a Hybrid of Man and Mouse Cells

An anonymous single copy X-chromosome clone, DXS79, from Xq26-Xq28, identifies a moderately frequent RFLP [HGM8 provisional no. DXS79]

Molecular and cytogenetic characterization of 9p- abnormalities

A method of processing first-trimester chorionic villous biopsies for cytogenetic analysis

Chromosome 3 duplication q/deletion p syndrome

Quinacrine Fluorescence for Identifying Metaphase Chromosomes, with Special Reference to Photomicrography

FISH diagnosis of partial trisomy 13 and tetrasomy 13 in a patient with severe trigonocephaly (C) phenotype

Trisomy 8 mosaicism syndrome

Complete and partial trisomy of different segments of chromosome 8: case reports and review

H-Y antigen negative patients with testicular tissue and 46,XY karyotype

Quinacrine Fluorescence Patterns of Human D Group Chromosomes

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