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Comparative genomic hybridization analysis of human oocytes and polar bodies

Human reproduction (Oxford), 2006-09, Vol.21 (9), p.2319-2328

2006

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Sequential FISH analysis of oocytes and polar bodies reveals aneuploidy mechanisms

Prenatal diagnosis, 2003-08, Vol.23 (8), p.663-668

2003

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Increased susceptibility to maternal aneuploidy demonstrated by comparative genomic hybridization analysis of human MII oocytes and first polar bodies

Cytogenetic and genome research, 2006-01, Vol.114 (1), p.30-38

2006

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Mechanisms of maternal aneuploidy : FISH analysis of oocytes and polar bodies in patients undergoing assisted conception

Human genetics, 2000-06, Vol.106 (6), p.620-626

2000

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Ascertainment and severity of Marfan syndrome in a Scottish population

Journal of medical genetics, 1994-01, Vol.31 (1), p.51-54

1994

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Trends in prenatal diagnosis of Down syndrome and other autosomal trisomies in Scotland 1990 to 1994, with associated cytogenetic and epidemiological findings

Genetic epidemiology, 1999, Vol.16 (2), p.179-190

1999

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Persistence of two Y chromosomes through meiotic prophase and metaphase I in an XYY man

Human genetics, 1991-08, Vol.87 (4), p.416-420

1991

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A cytogenetic survey of men being investigated for subfertility

Journal of reproduction & fertility, 1979-05, Vol.56 (1), p.209-216

1979

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Screening for Down's syndrome based on individual risk

BMJ, 1991-09, Vol.303 (6802), p.551-553

1991

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45,X/46,X dic (Y) mosaicism in a phenotypic male

Archives of disease in childhood, 1991-02, Vol.66 (2), p.252-253

1991

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Improved fragile site detection with trimethoprim

Human genetics, 1990-07, Vol.85 (2), p.241-243

1990

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Pericentric inversion of a group C autosome: a study of three families

Annals of human genetics, 1968-01, Vol.31 (3), p.219-230

1968

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Prenatal exclusion testing for Huntington's disease: a problem of too much information

Journal of medical genetics, 1989-02, Vol.26 (2), p.83-85

1989

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INHERITED PERICENTRIC INVERSION OF CHROMOSOME 5: A FAMILY WITH HISTORY OF NEONATAL DEATH AND A CASE OF THE “CRI DU CHAT” SYNDROME

Obstetrical & gynecological survey, 1973-06, Vol.28 (6), p.528

1973

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Features of di George syndrome in a child with 45,XX,-3,-22,+der(3),t(3;22)(p25;q11)

Journal of medical genetics, 1987-04, Vol.24 (4), p.225-227

1987

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Wiedemann-Beckwith syndrome in one of monozygotic twins

Archives of disease in childhood, 1985-12, Vol.60 (12), p.1191-1192

1985

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Nucleolus organiser regions on mitotic and meiotic chromosomes from infertile males investigated using a specific silver stain

Human genetics, 1979-01, Vol.48 (1), p.39-43

1979

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Chromosome abnormality in couples with histories of multiple abortions. The outcome of pregnancies subsequent to ascertainment and a study of familial translocation carriers

Human genetics, 1983-01, Vol.63 (1), p.45-47

1983

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A chromosome survey of a hospital for the mentally subnormal

Clinical genetics, 1979-09, Vol.16 (3), p.191-204

1979

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Sister chromatid exchange and chromosome aberration rates in a group of psoriatics before and after a course of PUVA treatment

British journal of dermatology (1951), 1980-09, Vol.103 (3), p.295-299

1980

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The effect of 8-methoxypsoralen and longwave UV-radiation on growth rates of human epidermal cells in culture

Experientia, 1983-02, Vol.39 (2), p.186-187

1983

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An XYY boy with short stature and a case of Klinefelter's syndrome (XXY) in a family with inversion 9

Clinical genetics, 1978-10, Vol.14 (4), p.241-245

1978

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Sister chromatid exchanges in human lymphocytes exposed to 8-methoxypsoralen and long wave UV radiation prior to incorporation of bromodeoxyuridine

Experientia, 1977-08, Vol.33 (8), p.1091-1093

1977

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Screening for Down's syndrome based on individual risk

British medical journal, 1991-09, Vol.303 (7 Sep 91), p.551-553

1991

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THE FETAL MANIFESTATIONS OF THE 45XO KARYOTYPE

BJOG : an international journal of obstetrics and gynaecology, 1969-03, Vol.76 (3), p.266-272

1969

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Comparative genomic hybridization analysis of human oocytes and polar bodies

Sequential FISH analysis of oocytes and polar bodies reveals aneuploidy mechanisms

Increased susceptibility to maternal aneuploidy demonstrated by comparative genomic hybridization analysis of human MII oocytes and first polar bodies

Mechanisms of maternal aneuploidy : FISH analysis of oocytes and polar bodies in patients undergoing assisted conception

Ascertainment and severity of Marfan syndrome in a Scottish population

Trends in prenatal diagnosis of Down syndrome and other autosomal trisomies in Scotland 1990 to 1994, with associated cytogenetic and epidemiological findings

Persistence of two Y chromosomes through meiotic prophase and metaphase I in an XYY man

A cytogenetic survey of men being investigated for subfertility

Screening for Down's syndrome based on individual risk

45,X/46,X dic (Y) mosaicism in a phenotypic male

Improved fragile site detection with trimethoprim

Pericentric inversion of a group C autosome: a study of three families

Prenatal exclusion testing for Huntington's disease: a problem of too much information

INHERITED PERICENTRIC INVERSION OF CHROMOSOME 5: A FAMILY WITH HISTORY OF NEONATAL DEATH AND A CASE OF THE “CRI DU CHAT” SYNDROME

Features of di George syndrome in a child with 45,XX,-3,-22,+der(3),t(3;22)(p25;q11)

Wiedemann-Beckwith syndrome in one of monozygotic twins

Nucleolus organiser regions on mitotic and meiotic chromosomes from infertile males investigated using a specific silver stain

Chromosome abnormality in couples with histories of multiple abortions. The outcome of pregnancies subsequent to ascertainment and a study of familial translocation carriers

A chromosome survey of a hospital for the mentally subnormal

Sister chromatid exchange and chromosome aberration rates in a group of psoriatics before and after a course of PUVA treatment

The effect of 8-methoxypsoralen and longwave UV-radiation on growth rates of human epidermal cells in culture

An XYY boy with short stature and a case of Klinefelter's syndrome (XXY) in a family with inversion 9

Sister chromatid exchanges in human lymphocytes exposed to 8-methoxypsoralen and long wave UV radiation prior to incorporation of bromodeoxyuridine

Screening for Down's syndrome based on individual risk

THE FETAL MANIFESTATIONS OF THE 45XO KARYOTYPE

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