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J M Connor

Showing results (171-180 of 181) with videos related to

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Annals of the New York Academy of Sciences|January 1, 1991
Genetic heterogeneity in tuberous sclerosis. Study of a large collaborative datasetJ L Haines, J Amos, J Attwood, et al.
Journal of Hypertension|May 1, 1992
Abnormalities of glucocorticoid metabolism and the renin-angiotensin system: a four-corners approach to the identification of genetic determinants of blood pressureG C Watt, S B Harrap, C J Foy, et al.
American Journal of Human Genetics|April 1, 1987
Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardationM H Hofker, A A Bergen, M I Skraastad, et al.
Human Molecular Genetics|November 1, 1992
A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genesA P Walker, J Chelly, D R Love, et al.
Journal of Medical Genetics|December 1, 1991
Genotype prediction in the fragile X syndromeM C Hirst, Y Nakahori, S J Knight, et al.
The New England Journal of Medicine|May 9, 1996
Dimeric inhibin A as a marker for Down's syndrome in early pregnancyD A Aitken, E M Wallace, J A Crossley, et al.
Journal of Medical Genetics|May 1, 1990
Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probesA Cooke, W G Lanyon, D E Wilcox, et al.
American Journal of Human Genetics|August 1, 1997
Evidence for a familial pregnancy-induced hypertension locus in the eNOS-gene regionR Arngrímsson, C Hayward, S Nadaud, et al.
American Journal of Human Genetics|January 13, 2000
Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31G Feldman, M Li, S Martin, et al.
Clinical Genetics|November 15, 2000
Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP)M Q Xu, G Feldman, M Le Merrer, et al.
Pageof 19

Showing results (171-180 of 181) with videos related to

Sort By:
Pageof 19
Annals of the New York Academy of Sciences|January 1, 1991
Genetic heterogeneity in tuberous sclerosis. Study of a large collaborative datasetJ L Haines, J Amos, J Attwood, et al.
Journal of Hypertension|May 1, 1992
Abnormalities of glucocorticoid metabolism and the renin-angiotensin system: a four-corners approach to the identification of genetic determinants of blood pressureG C Watt, S B Harrap, C J Foy, et al.
American Journal of Human Genetics|April 1, 1987
Efficient isolation of X chromosome-specific single-copy probes from a cosmid library of a human X/hamster hybrid-cell line: mapping of new probes close to the locus for X-linked mental retardationM H Hofker, A A Bergen, M I Skraastad, et al.
Human Molecular Genetics|November 1, 1992
A YAC contig in Xp21 containing the adrenal hypoplasia congenita and glycerol kinase deficiency genesA P Walker, J Chelly, D R Love, et al.
Journal of Medical Genetics|December 1, 1991
Genotype prediction in the fragile X syndromeM C Hirst, Y Nakahori, S J Knight, et al.
The New England Journal of Medicine|May 9, 1996
Dimeric inhibin A as a marker for Down's syndrome in early pregnancyD A Aitken, E M Wallace, J A Crossley, et al.
Journal of Medical Genetics|May 1, 1990
Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probesA Cooke, W G Lanyon, D E Wilcox, et al.
American Journal of Human Genetics|August 1, 1997
Evidence for a familial pregnancy-induced hypertension locus in the eNOS-gene regionR Arngrímsson, C Hayward, S Nadaud, et al.
American Journal of Human Genetics|January 13, 2000
Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31G Feldman, M Li, S Martin, et al.
Clinical Genetics|November 15, 2000
Linkage exclusion and mutational analysis of the noggin gene in patients with fibrodysplasia ossificans progressiva (FOP)M Q Xu, G Feldman, M Le Merrer, et al.
Pageof 19