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Human Genetics|August 1, 1992
Physical fine mapping of genes underlying X-linked deafness and non fra (X)-X-linked mental retardation at Xq21I Bach, D Robinson, N Thomas, et al.Human Genetics|August 1, 1992
Molecular studies of parental origin and mosaicism in 45,X conceptusesT Hassold, D Pettay, A Robinson, et al.Human Genetics|May 6, 2004
Lipoprotein lipase gene is in linkage with blood pressure phenotypes in Chinese pedigreesWenjie Yang, Jianfeng Huang, Dongliang Ge, et al.Human Genetics|March 12, 2004
Extended haplotype analysis in the HLA complex reveals an increased frequency of the HFE-C282Y mutation in individuals with multiple sclerosisJustin P Rubio, Melanie Bahlo, Niall Tubridy, et al.Human Genetics|March 12, 2004
SNURF-SNRPN and UBE3A transcript levels in patients with Angelman syndromeMaren Runte, Peter M Kroisel, Gabriele Gillessen-Kaesbach, et al.Human Genetics|March 23, 2004
Variants of CYP46A1 may interact with age and APOE to influence CSF Abeta42 levels in Alzheimer's diseaseAnnica Johansson, Hagit Katzov, Henrik Zetterberg, et al.Human Genetics|March 23, 2004
Fine mapping of the Schnyder's crystalline corneal dystrophy locusVeena Theendakara, Gerard Tromp, Helena Kuivaniemi, et al.Human Genetics|March 17, 2004
A new locus for autosomal dominant Charcot-Marie-Tooth disease type 2 (CMT2L) maps to chromosome 12q24Bei-Sha Tang, Wei Luo, Kun Xia, et al.Human Genetics|September 29, 2005
Comprehensive genetic evaluation of common E-cadherin sequence variants and prostate cancer risk: strong confirmation of functional promoter SNPSara Lindström, Fredrik Wiklund, Björn-Anders Jonsson, et al.Human Genetics|September 29, 2005
Identification of a locus for nongoitrous congenital hypothyroidism on chromosome 15q25.3-26.1Helmut Grasberger, Martine Vaxillaire, Silvana Pannain, et al.Pageof 957