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J Feingold

Showing results (251-260 of 307) with videos related to

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Human Genetics|January 1, 1996
Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: implications for mapping the hemochromatosis gene (HFE)G Gandon, A M Jouanolle, B Chauvel, et al.
Annales De Genetique|January 9, 1999
Prevalence of the C282Y mutation in Brittany: penetrance of genetic hemochromatosis?A M Jouanolle, P Fergelot, M L Raoul, et al.
Human Genetics|February 1, 1991
Spectrum of phenylketonuria mutations in western Europe and north Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locusM Berthelon, C Caillaud, F Rey, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|November 1, 1993
Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysisC Dodé, A Dürr, C Pêcheux, et al.
Psychiatry Research|October 1, 1990
Subtyping familial schizophrenia: reliability, concordance, and stabilityM Leboyer, M Jay, T D'Amato, et al.
Nature|November 24, 1988
Unusual segregation of cystic fibrosis allelesA Kitzis, J C Chomel, A Haliassos, et al.
Therapie|January 1, 1993
[Collection of familial data in pharmacogenetics. Methodological problems]N Poisson, Y Bechtel, P De La Selle, et al.
American Journal of Hematology|November 3, 1998
Hemoglobins in Togolese newborns: Hb S, Hb C, Hb Bart's, and alpha-globin gene statusA Y Segbena, C Prehu, H Wajcman, et al.
Journal of Medical Genetics|September 1, 1996
A duplication of distal Xp associated with hypogonadotrophic hypogonadism, hypoplastic external genitalia, mental retardation, and multiple congenital abnormalitiesL Telvi, A Ion, J C Carel, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 11, 1991
A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkageJ S Beckmann, I Richard, D Hillaire, et al.
Pageof 31

Showing results (251-260 of 307) with videos related to

Sort By:
Pageof 31
Human Genetics|January 1, 1996
Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region: implications for mapping the hemochromatosis gene (HFE)G Gandon, A M Jouanolle, B Chauvel, et al.
Annales De Genetique|January 9, 1999
Prevalence of the C282Y mutation in Brittany: penetrance of genetic hemochromatosis?A M Jouanolle, P Fergelot, M L Raoul, et al.
Human Genetics|February 1, 1991
Spectrum of phenylketonuria mutations in western Europe and north Africa, and their relation to polymorphic DNA haplotypes at the phenylalanine hydroxylase locusM Berthelon, C Caillaud, F Rey, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|November 1, 1993
Huntington's disease in French families: CAG repeat expansion and linkage disequilibrium analysisC Dodé, A Dürr, C Pêcheux, et al.
Psychiatry Research|October 1, 1990
Subtyping familial schizophrenia: reliability, concordance, and stabilityM Leboyer, M Jay, T D'Amato, et al.
Nature|November 24, 1988
Unusual segregation of cystic fibrosis allelesA Kitzis, J C Chomel, A Haliassos, et al.
Therapie|January 1, 1993
[Collection of familial data in pharmacogenetics. Methodological problems]N Poisson, Y Bechtel, P De La Selle, et al.
American Journal of Hematology|November 3, 1998
Hemoglobins in Togolese newborns: Hb S, Hb C, Hb Bart's, and alpha-globin gene statusA Y Segbena, C Prehu, H Wajcman, et al.
Journal of Medical Genetics|September 1, 1996
A duplication of distal Xp associated with hypogonadotrophic hypogonadism, hypoplastic external genitalia, mental retardation, and multiple congenital abnormalitiesL Telvi, A Ion, J C Carel, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|January 11, 1991
A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkageJ S Beckmann, I Richard, D Hillaire, et al.
Pageof 31