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Molecular genetic analysis of the APEX nuclease gene in amyotrophic lateral sclerosis

Neurology, 1999-06, Vol.52 (9), p.1899-1899

1999

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Evidence for a Familial Pregnancy-Induced Hypertension Locus in the eNOS-Gene Region

American journal of human genetics, 1997-08, Vol.61 (2), p.354-362

1997

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Increased energy expenditure in cystic fibrosis is associated with specific mutations

Clinical science (1979), 1992-01, Vol.82 (1), p.71-76

1992

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Carrier screening in the community

Journal of inherited metabolic disease, 1995-07, Vol.18 (4), p.525-532

Brock, D. J. H.

1995

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Homozygosity for Asn86Ser mutation in the CuZn-superoxide dismutase gene produces a severe clinical phenotype in a juvenile onset case of familial amyotrophic lateral sclerosis

Journal of medical genetics, 1998-02, Vol.35 (2), p.174-174

1998

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Prenatal cystic fibrosis carrier screening: Factors in a woman's decision to decline testing

Prenatal diagnosis, 1993-09, Vol.13 (9), p.807-814

1993

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Three novel mutations in the cystic fibrosis gene detected by chemical cleavage: analysis of variant splicing and a nonsense mutation

Human molecular genetics, 1992-04, Vol.1 (1), p.11-17

1992

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A study of the Huntington's disease associated trinucleotide repeat in the Scottish population

Journal of medical genetics, 1993-12, Vol.30 (12), p.1003-1007

1993

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P67L: a cystic fibrosis allele with mild effects found at high frequency in the Scottish population

Journal of medical genetics, 1998-02, Vol.35 (2), p.122-125

1998

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Prenatal screening for cystic fibrosis: psychological effects on carriers and their partners

Journal of medical genetics, 1993-07, Vol.30 (7), p.543-548

1993

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Presymptomatic testing for Huntington's disease: a case complicated by recombination within the D4S10 locus

Human genetics, 1989, Vol.81 (2), p.188-190

1989

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Two novel mutations and a neutral polymorphism in EGF-like domains of the fibrillin gene (FBN1): SSCP screening of exons 15–21 in Marfan syndrome patients

Human molecular genetics, 1994-02, Vol.3 (2), p.373-375

1994

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Pregabalin for treatment of generalized anxiety disorder: a 4-week, multicenter, double-blind, placebo-controlled trial of pregabalin and alprazolam

Archives of general psychiatry, 2005-09, Vol.62 (9), p.1022

2005

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Huntington's disease in a Sudanese family from Khartoum

Human genetics, 1995-11, Vol.96 (5), p.624-625

1995

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First-trimester prenatal diagnosis of cystic fibrosis using fibroblasts from a deceased index child to establish haplotypes

Prenatal diagnosis, 1988-10, Vol.8 (8), p.625-628

1988

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Heterozygote Screening for Cystic Fibrosis

Journal of medical screening, 1994-04, Vol.1 (2), p.130-134

Brock, D J H

1994

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Presymptomatic testing for autosomal dominant spinocerebellar ataxia type 1

Journal of medical genetics, 1993-07, Vol.30 (7), p.616-617

1993

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Changes in maternal age distribution and their possible impact on demand for prenatal diagnostic services

BMJ, 1988-04, Vol.296 (6627), p.978-981

1988

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Friedreich's ataxia, with retained lower limb tendon reflexes, in a Saudi Arabian family

Clinical neurology and neurosurgery, 1996-02, Vol.98 (1), p.8-11

1996

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Prenatal exclusion testing for Huntington disease using the polymerase chain reaction

American journal of medical genetics, 1989-02, Vol.32 (2), p.274-276

1989

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Screening Alzheimer's disease patients for mutations in the amyloid precursor protein gene

Molecular and cellular probes, 1993-04, Vol.7 (2), p.161-165

1993

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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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A monoclonal antibody-based immunoassay for human lactoferrin

Journal of immunological methods, 1985-11, Vol.84 (1), p.135-141

1985

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Prenatal diagnosis and screening: present and future

Progress in clinical and biological research, 1985, Vol.163A, p.107

Brock, D J

1985

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Population screening for cystic fibrosis

Current opinion in pediatrics, 1996-12, Vol.8 (6), p.635-638

Brock, D J

1996

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Molecular genetic analysis of the APEX nuclease gene in amyotrophic lateral sclerosis

Evidence for a Familial Pregnancy-Induced Hypertension Locus in the eNOS-Gene Region

Increased energy expenditure in cystic fibrosis is associated with specific mutations

Carrier screening in the community

Homozygosity for Asn86Ser mutation in the CuZn-superoxide dismutase gene produces a severe clinical phenotype in a juvenile onset case of familial amyotrophic lateral sclerosis

Prenatal cystic fibrosis carrier screening: Factors in a woman's decision to decline testing

Three novel mutations in the cystic fibrosis gene detected by chemical cleavage: analysis of variant splicing and a nonsense mutation

A study of the Huntington's disease associated trinucleotide repeat in the Scottish population

P67L: a cystic fibrosis allele with mild effects found at high frequency in the Scottish population

Prenatal screening for cystic fibrosis: psychological effects on carriers and their partners

Presymptomatic testing for Huntington's disease: a case complicated by recombination within the D4S10 locus

Two novel mutations and a neutral polymorphism in EGF-like domains of the fibrillin gene (FBN1): SSCP screening of exons 15–21 in Marfan syndrome patients

Pregabalin for treatment of generalized anxiety disorder: a 4-week, multicenter, double-blind, placebo-controlled trial of pregabalin and alprazolam

Huntington's disease in a Sudanese family from Khartoum

First-trimester prenatal diagnosis of cystic fibrosis using fibroblasts from a deceased index child to establish haplotypes

Heterozygote Screening for Cystic Fibrosis

Presymptomatic testing for autosomal dominant spinocerebellar ataxia type 1

Changes in maternal age distribution and their possible impact on demand for prenatal diagnostic services

Friedreich's ataxia, with retained lower limb tendon reflexes, in a Saudi Arabian family

Prenatal exclusion testing for Huntington disease using the polymerase chain reaction

Screening Alzheimer's disease patients for mutations in the amyloid precursor protein gene

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

A monoclonal antibody-based immunoassay for human lactoferrin

Prenatal diagnosis and screening: present and future

Population screening for cystic fibrosis

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