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Deletion of chromosome 3q proximal region gives rise to a variable phenotype

Clinical genetics, 1998-03, Vol.53 (3), p.220-222

1998

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FALSE POSITIVE IN PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS

The Lancet (British edition), 1988-06, Vol.331 (8598), p.1333-1334

1988

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A nonsense mutation of the human luteinizing hormone receptor gene in Leydig cell hypoplasia

Human molecular genetics, 1995-08, Vol.4 (8), p.1429-1433

1995

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UROGENITAL MALFORMATIONS AND DISEASE

British medical bulletin, 1986-04, Vol.42 (2), p.181-186

1986

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Inactivation of the Luteinizing Hormone/Chorionic Gonadotropin Receptor by an Insertional Mutation in Leydig Cell Hypoplasia

Molecular endocrinology (Baltimore, Md.), 1998-11, Vol.12 (11), p.1651-1660

1998

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The use of non-metrical variations of the cranium in the study of Scandinavian population movements

American journal of physical anthropology, 1974-05, Vol.40 (3), p.345-358

Berry, A. Caroline

1974

Volltextzugriff (PDF)

The anthropological value of minor variants of the dental crown

American journal of physical anthropology, 1976-09, Vol.45 (2), p.257-267

Berry, A. Caroline

1976

Volltextzugriff (PDF)

Chromosome 15 in floppy infants

Archives of disease in childhood, 1981-11, Vol.56 (11), p.882-885

1981

Volltextzugriff (PDF)

Fraser syndrome: Diagnosed in a 50-year-old museum specimen

American journal of medical genetics, 2000-09, Vol.94 (3), p.262-264

2000

Volltextzugriff (PDF)

Case Report: Partial trisomy of 15q due to inserted inverted duplication

Clinical genetics, 1997-12, Vol.52 (6), p.442-445

1997

Volltextzugriff (PDF)

Ask the expert

Pediatric nephrology (Berlin, West), 1991, Vol.5 (6), p.684-684

Berry, A. Caroline

1991

Volltextzugriff (PDF)

Partial trisomy of 15q due to inserted inverted duplication

Clinical genetics, 1997-12, Vol.52 (6), p.442-445

1997

Volltextzugriff (PDF)

COMPOUND HETEROZYGOUS MUTATIONS OF THE LUTEINIZING HORMONE/CHORIONIC GONADOTROPIN RECEPTOR GENE IN A FAMILY WITH TWO CHILDREN AFFECTED BY LEYDIG CELL HYPOPLASIA (LCH). • 387

Pediatric research, 1997-04, Vol.41, p.67-67

1997

Volltextzugriff (PDF)

Genetical Change in Ancient Egypt

Man (London), 1967-12, Vol.2 (4), p.551-568

1967

Volltextzugriff (PDF)

Screening for Fragile X

Journal of medical screening, 1997, Vol.4 (4), p.247-247

Berry, A Caroline

1997

Volltextzugriff (PDF)

A fetus with an X;1 balanced reciprocal translocation and eye disease

Journal of medical genetics, 1995-07, Vol.32 (7), p.557-560

1995

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Prenatal diagnostic amniocentesis: problems with interpretation of unusual karyotypes

Journal of obstetrics and gynaecology, 1982, Vol.2 (4), p.197-202

Berry, A. Caroline

1982

Volltextzugriff (PDF)

FALSE POSITIVE ACETYLCHOLINESTERASE GEL TEST

The Lancet (British edition), 1981-02, Vol.317 (8217), p.444-444

1981

Volltextzugriff (PDF)

12 - Chromosome Analysis and Buccal Smear

Endocrine Disorders, 1984, p.127-132

Berry, A. Caroline

1984

Volltextzugriff (PDF)

AMNIOTIC-FLUID ALPHA-FETOPROTEIN AND FETAL RENAL AGENESIS

The Lancet (British edition), 1978-03, Vol.311 (8065), p.660-660

1978

Volltextzugriff (PDF)

Molecular genetics for the clinicianD.J.H. Brock cambridge University Press, 1993 £35.00 hbk/£15.95 pbk (289 pages) ISBN 0 521 41179 3

Trends in Genetics, 1993, Vol.9 (7), p.256-257

Caroline Berry, A.

1993

Volltextzugriff (PDF)

Molecular genetics for the clinician: D.J.H. Brock cambridge University Press, 1993 £35.00 hbk/£15.95 pbk (289 pages) ISBN 0 521 41179 3

Trends in Genetics, 1993, Vol.9 (7), p.256-257

Caroline Berry, A.

1993

Volltextzugriff (PDF)

GENETIC COUNSELLING FOR THE BLIND

The Lancet (British edition), 1982-07, Vol.320 (8289), p.106-107

1982

Volltextzugriff (PDF)

Case Report: Partial trisomy of 15q due to inserted inverted duplication

Clinical Genetics, 1997, Vol.52 (6), p.442-445

1997

Volltextzugriff (PDF)

Secrets in the Genes

Journal of Medical Genetics, 1995, Vol.32 (12), p.999-999

Berry, A Caroline

1995

Volltextzugriff (PDF)

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Deletion of chromosome 3q proximal region gives rise to a variable phenotype

FALSE POSITIVE IN PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS

A nonsense mutation of the human luteinizing hormone receptor gene in Leydig cell hypoplasia

UROGENITAL MALFORMATIONS AND DISEASE

Inactivation of the Luteinizing Hormone/Chorionic Gonadotropin Receptor by an Insertional Mutation in Leydig Cell Hypoplasia

The use of non-metrical variations of the cranium in the study of Scandinavian population movements

The anthropological value of minor variants of the dental crown

Chromosome 15 in floppy infants

Fraser syndrome: Diagnosed in a 50-year-old museum specimen

Case Report: Partial trisomy of 15q due to inserted inverted duplication

Ask the expert

Partial trisomy of 15q due to inserted inverted duplication

COMPOUND HETEROZYGOUS MUTATIONS OF THE LUTEINIZING HORMONE/CHORIONIC GONADOTROPIN RECEPTOR GENE IN A FAMILY WITH TWO CHILDREN AFFECTED BY LEYDIG CELL HYPOPLASIA (LCH). • 387

Genetical Change in Ancient Egypt

Screening for Fragile X

A fetus with an X;1 balanced reciprocal translocation and eye disease

Prenatal diagnostic amniocentesis: problems with interpretation of unusual karyotypes

FALSE POSITIVE ACETYLCHOLINESTERASE GEL TEST

12 - Chromosome Analysis and Buccal Smear

AMNIOTIC-FLUID ALPHA-FETOPROTEIN AND FETAL RENAL AGENESIS

Molecular genetics for the clinicianD.J.H. Brock cambridge University Press, 1993 £35.00 hbk/£15.95 pbk (289 pages) ISBN 0 521 41179 3

Molecular genetics for the clinician: D.J.H. Brock cambridge University Press, 1993 £35.00 hbk/£15.95 pbk (289 pages) ISBN 0 521 41179 3

GENETIC COUNSELLING FOR THE BLIND

Case Report: Partial trisomy of 15q due to inserted inverted duplication

Secrets in the Genes

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