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Mutation in codon 713 of the β amyloid precursor protein gene presenting with schizophrenia

Nature genetics, 1992-07, Vol.1 (4), p.306-309

1992

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Psychological impact of population-based carrier testing for cystic fibrosis: 3-year follow-up

The Lancet (British edition), 1996-05, Vol.347 (9013), p.1443-1446

1996

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Prenatal screening for cystic fibrosis: 5 years' experience reviewed

The Lancet (British edition), 1996-01, Vol.347 (8995), p.148-150

Brock, D.J.H

1996

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A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomes

Molecular and cellular probes, 1993-06, Vol.7 (3), p.235-239

1993

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Prenatal screening for cystic fibrosis

The Lancet (British edition), 1992-07, Vol.340 (8813), p.214-216

1992

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Heterogeneity analysis in 40 X-linked retinitis pigmentosa families

American journal of human genetics, 1994-07, Vol.55 (1), p.105-111

1994

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35. Antenatal screening for cystic fibrosis: The Edinburgh experience

Netherlands journal of medicine, 1999-06, Vol.54, p.S32

GILFILLAN, A

1999

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Non-paternity and prenatal genetic screening

The Lancet (British edition), 1991-11, Vol.338 (8775), p.1151-1151

1991

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Screening for cystic fibrosis carriers

The Lancet (British edition), 1992-10, Vol.340 (8825), p.984-984

Brock, D.J.H.

1992

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Genetic hetergoeneity in X-linked hydrocephalus: Linkage to markers within Xq27. 3

American journal of human genetics, 1994-02, Vol.54:2

1994

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MORPHOLOGY OF RAPIDLY ADHERING AMNIOTIC-FLUID CELLS AS AN AID TO THE DIAGNOSIS OF NEURAL-TUBE DEFECTS

The Lancet (British edition), 1977-04, Vol.309 (8018), p.919-922

1977

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Superoxide dismutase and amyotrophic lateral sclerosis

The Lancet (British edition), 1995-02, Vol.345 (8946), p.391-391

1995

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Smal and Hha l polymorphisms in the 5′ region of the human von Willebrand factor gene (F8VWF)

Nucleic acids research, 1991, Vol.19 (14), p.4017-4017

1991

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ALPHA-FETOPROTEIN IN THE ANTENATAL DIAGNOSIS OF ANENCEPHALY AND SPINA BIFIDA

The Lancet (British edition), 1972-07, Vol.300 (7770), p.197-199

1972

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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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Fertility of older women

The Lancet (British edition), 1990-06, Vol.335 (8703), p.1470-1470, Article 1470

1990

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PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS

The Lancet (British edition), 1985-07, Vol.326 (8445), p.47-48

1985

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RAPID METHOD FOR THE EXCLUSION OF FETAL NEURAL-TUBE DEFECTS

The Lancet (British edition), 1981-08, Vol.318 (8244), p.468-468

Brock, D.J.H.

1981

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Detection of the Z antitrypsin ( 1AT) genotype in chronic liver disease by analysis of amplified DNA sequences

Journal of hepatology, 1989-07, Vol.9 (1), p.P10-P10

1989

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MECHANISMS BY WHICH AMNIOTIC-FLUID ALPHA-FETOPROTEIN MAY BE INCREASED IN FETAL ABNORMALITIES

The Lancet (British edition), 1976-08, Vol.308 (7981), p.345-346

Brock, D.J.H.

1976

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Cystic fibrosis screening policies

The Lancet (British edition), 1996-04, Vol.347 (9006), p.969-969

1996

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A Simple Method for Ranking the Affinities of Monoclonal Antibodies

Journal of immunological methods, 1983-01, Vol.62 (2), p.147-153

1983

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Gene/energy interaction in cystic fibrosis

The Lancet (British edition), 1990-03, Vol.335 (8688), p.552-553

1990

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Use of stable dye-DNA intercalating complexes to detect cystic fibrosis mutations

Molecular and cellular probes, 1994-06, Vol.8 (3), p.245-250

1994

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SmaI and HhaI polymorphisms in the 5' region of the human von Willebrand factor gene (F8VWF)

Nucleic acids research, 1991-07, Vol.19 (14), p.4017-4017

1991

Volltextzugriff (PDF)

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Mutation in codon 713 of the β amyloid precursor protein gene presenting with schizophrenia

Psychological impact of population-based carrier testing for cystic fibrosis: 3-year follow-up

Prenatal screening for cystic fibrosis: 5 years' experience reviewed

A new polymerase chain reaction (PCR) assay for the trinucleotide repeat that is unstable and expanded on Huntington's disease chromosomes

Prenatal screening for cystic fibrosis

Heterogeneity analysis in 40 X-linked retinitis pigmentosa families

35. Antenatal screening for cystic fibrosis: The Edinburgh experience

Non-paternity and prenatal genetic screening

Screening for cystic fibrosis carriers

Genetic hetergoeneity in X-linked hydrocephalus: Linkage to markers within Xq27. 3

MORPHOLOGY OF RAPIDLY ADHERING AMNIOTIC-FLUID CELLS AS AN AID TO THE DIAGNOSIS OF NEURAL-TUBE DEFECTS

Superoxide dismutase and amyotrophic lateral sclerosis

Smal and Hha l polymorphisms in the 5′ region of the human von Willebrand factor gene (F8VWF)

ALPHA-FETOPROTEIN IN THE ANTENATAL DIAGNOSIS OF ANENCEPHALY AND SPINA BIFIDA

Huntington's disease in a Sudanese family from Khartoum

Fertility of older women

PRENATAL DIAGNOSIS OF CYSTIC FIBROSIS

RAPID METHOD FOR THE EXCLUSION OF FETAL NEURAL-TUBE DEFECTS

Detection of the Z antitrypsin ( 1AT) genotype in chronic liver disease by analysis of amplified DNA sequences

MECHANISMS BY WHICH AMNIOTIC-FLUID ALPHA-FETOPROTEIN MAY BE INCREASED IN FETAL ABNORMALITIES

Cystic fibrosis screening policies

A Simple Method for Ranking the Affinities of Monoclonal Antibodies

Gene/energy interaction in cystic fibrosis

Use of stable dye-DNA intercalating complexes to detect cystic fibrosis mutations

SmaI and HhaI polymorphisms in the 5' region of the human von Willebrand factor gene (F8VWF)

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