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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

Volltextzugriff (PDF)

DNA polymorphism and the study of disease associations

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

1988

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Clayton, F J

2016

Volltextzugriff (PDF)

A LIKELIHOOD APPROACH TO HLA SEROLOGY

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

1992

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Interpretation of RFLP linkage data

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

Clayton, J F

1984

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Radioisotope Instruments: International Series of Monographs in Nuclear Energy

2013

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Linkage heterogeneity and fragile X

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

1988

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

A genetic linkage study of choroideremia

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

1986

Volltextzugriff (PDF)

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

British medical journal (Clinical research ed.), 1986-11, Vol.293 (6555), p.1174

1986

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Oestrogens and coronary artery disease in men

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

1983

Volltextzugriff (PDF)

Periodical Literature

Antiquaries journal, 1970-09, Vol.50 (2), p.409-418

Clayton, J. F.

1970

Volltextzugriff (PDF)

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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

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

A LIKELIHOOD APPROACH TO HLA SEROLOGY

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

Radioisotope Instruments: International Series of Monographs in Nuclear Energy

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

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

Oestrogens and coronary artery disease in men

Periodical Literature

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