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Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

Nature (London), 1984-05, Vol.309 (5965), p.253-255

1984

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DNA polymorphism and the study of disease associations

Human genetics, 1988-04, Vol.78 (4), p.299-312

1988

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Mortality ratios, life expectancy, and causes of death in patients with Turner's syndrome

Journal of epidemiology and community health (1979), 1986-06, Vol.40 (2), p.97-102

1986

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Causes of death in X chromatin positive males (Klinefelter's syndrome)

Journal of epidemiology and community health (1979), 1985-12, Vol.39 (4), p.330-336

1985

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A computer programme to calculate risk in X linked disorders using multiple marker loci

Journal of medical genetics, 1986-02, Vol.23 (1), p.35-39

Clayton, J F

1986

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A LIKELIHOOD APPROACH TO HLA SEROLOGY

European journal of immunogenetics, 1992-10, Vol.19 (5), p.311-322

1992

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Automatic integration of letters and speech-sounds in typical reading development and dyslexia

Clayton, F J

2016

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A study into possible deviation from the Hardy-Weinberg equilibrium by the alleles of the hypervariable sequence in the region of the human insulin gene

Clinical genetics, 1986-10, Vol.30 (4), p.293-297

1986

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Interpretation of RFLP linkage data

Journal of medical genetics, 1984-04, Vol.21 (2), p.157-158

Clayton, J F

1984

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Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 {L1.28}: further linkage data, heterogeneity testing, and risk estimation

Human genetics, 1986-10, Vol.74 (2), p.168-171

1986

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Studies of genetic linkage between adult polycystic kidney disease and three markers on chromosome 16

Journal of medical genetics, 1987-08, Vol.24 (8), p.457-461

1987

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A genetic linkage study of a kindred with X-linked retinitis pigmentosa

British journal of ophthalmology, 1985-05, Vol.69 (5), p.340-347

1985

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Linkage heterogeneity and fragile X

Human genetics, 1988-04, Vol.78 (4), p.338-342

1988

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Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

Nature (London), 1984-01, Vol.309 (5965), p.253-255

1984

Volltextzugriff (PDF)

Mortality and causes of death in females with extra X chromosomes and males with extra Y chromosomes

Journal of epidemiology and community health (1979), 1987-03, Vol.41 (1), p.1-4

1987

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Mortality ratios and life expectancy in X chromatin positive males

Journal of epidemiology and community health (1979), 1985-03, Vol.39 (1), p.33-38

1985

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A genetic linkage study of choroideremia

Ophthalmic genetics, 1986, Vol.7 (3), p.201-204

1986

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Prenatal diagnosis of Turner's syndrome: what to tell parents

BMJ, 1986-11, Vol.293 (6555), p.1174-1174

1986

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Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14

American journal of human genetics, 1987-10, Vol.41 (4), p.635-644

1987

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Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal Xq

Human genetics, 1987-06, Vol.76 (2), p.165-172

1987

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Multipoint linkage analysis of steroid sulfatase (X-linked ichthyosis) and distal Xp markers

Genomics (San Diego, Calif.), 1987-09, Vol.1 (1), p.52-59

1987

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ABSTRACT: Regional Trends and Exploration Potential for Coal Bed Methane in Louisiana

AAPG bulletin, 2002, Vol.86

F. Clayton Breland1, Chacko J. John

2002

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A computer programme to calculate risk in X linked disorders using multiple marker loci

Journal of medical genetics, 1986-01, Vol.23 (1), p.38-39

Clayton, J F

1986

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Oestrogens and coronary artery disease in men

The Lancet (British edition), 1983-10, Vol.2 (8354), p.860-861

1983

Volltextzugriff (PDF)

List of Accessions

Antiquaries journal, 1970-09, Vol.50 (2), p.400-408

Clayton, J. F.

1970

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Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

DNA polymorphism and the study of disease associations

Mortality ratios, life expectancy, and causes of death in patients with Turner's syndrome

Causes of death in X chromatin positive males (Klinefelter's syndrome)

A computer programme to calculate risk in X linked disorders using multiple marker loci

A LIKELIHOOD APPROACH TO HLA SEROLOGY

Automatic integration of letters and speech-sounds in typical reading development and dyslexia

A study into possible deviation from the Hardy-Weinberg equilibrium by the alleles of the hypervariable sequence in the region of the human insulin gene

Interpretation of RFLP linkage data

Genetic linkage between X-linked retinitis pigmentosa and DNA probe DXS7 {L1.28}: further linkage data, heterogeneity testing, and risk estimation

Studies of genetic linkage between adult polycystic kidney disease and three markers on chromosome 16

A genetic linkage study of a kindred with X-linked retinitis pigmentosa

Linkage heterogeneity and fragile X

Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

Mortality and causes of death in females with extra X chromosomes and males with extra Y chromosomes

Mortality ratios and life expectancy in X chromatin positive males

A genetic linkage study of choroideremia

Prenatal diagnosis of Turner's syndrome: what to tell parents

Linkage relationships between X-linked retinitis pigmentosa and nine short-arm markers: exclusion of the disease locus from Xp21 and localization to between DXS7 and DXS14

Ten families with fragile X syndrome: linkage relationships with four DNA probes from distal Xq

Multipoint linkage analysis of steroid sulfatase (X-linked ichthyosis) and distal Xp markers

ABSTRACT: Regional Trends and Exploration Potential for Coal Bed Methane in Louisiana

A computer programme to calculate risk in X linked disorders using multiple marker loci

Oestrogens and coronary artery disease in men

List of Accessions

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