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Human Genetics|November 3, 1998
Variant in sulfonylurea receptor-1 gene is associated with high insulin concentrations in non-diabetic Mexican Americans: SUR-1 gene variant and hyperinsulinemiaD L Goksel, K Fischbach, R Duggirala, et al.Human Genetics|November 3, 1998
New mechanism of BRCA-1 mutation by deletion/insertion at the same nucleotide position in three unrelated French breast/ovarian cancer familiesN Presneau, V Laplace-Marieze, V Sylvain, et al.Human Genetics|December 7, 2007
Comments on the entropy-based transmission/disequilibrium testWarren Ewens, Mingyao LiHuman Genetics|January 4, 2008
Blue eye color in humans may be caused by a perfectly associated founder mutation in a regulatory element located within the HERC2 gene inhibiting OCA2 expressionHans Eiberg, Jesper Troelsen, Mette Nielsen, et al.Human Genetics|January 4, 2008
Nonsense-mediated messenger RNA decay of survival motor neuron 1 causes spinal muscular atrophyLars Brichta, Lutz Garbes, Maria Jedrzejowska, et al.Human Genetics|January 4, 2008
Genetic variation in CYP17 and endometrial cancer riskMia M Gaudet, James V Lacey, Jolanta Lissowska, et al.Human Genetics|October 14, 1977
The frequency and distribution of sister chromatid exchanges in human chromosomesW F Morgan, P E CrossenHuman Genetics|October 14, 1977
Intellectual level (IQ) in heterozygotes for phenylketonuria (PKU). Is the PKU gene also acting by means other than phenylalanine-blood level elevation?O Thalhammer, L Havelec, E Knoll, et al.Human Genetics|October 14, 1977
LBA technique in the detection of chromosome variants. II. Chromosomes except for those with Q variantsY Nakagome, S Oka, E MatsunagaHuman Genetics|May 1, 1997
Possible association of the allele status of the CS.7/HhaI polymorphism 5' of the CFTR gene with postnatal female survivalM Macek, M Macek, A Krebsová, et al.Pageof 957