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Human Genetics|December 1, 1991
Exclusion of COL1A1, COL1A2, and COL3A1 genes as candidate genes for Ehlers-Danlos syndrome type I in one large familyB P Sokolov, A N Prytkov, G Tromp, et al.Human Genetics|July 19, 2006
Confirmation of linkage to chromosome 1q for spine bone mineral density in southern ChineseChing-Lung Cheung, Qing-Yang Huang, Mandy Y M Ng, 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.Human Genetics|March 3, 2007
Candidate SNPs for a universal individual identification panelAndrew J Pakstis, William C Speed, Judith R Kidd, et al.Human Genetics|January 1, 1992
Parental origin and germline mosaicism of deletions and duplications of the dystrophin gene: a European studyA J van Essen, S Abbs, M Baiget, et al.Human Genetics|June 1, 1991
Ehlers-Danlos syndrome type VII: a single base change that causes exon skipping in the type I collagen alpha 2(I) chainA C Nicholls, J Oliver, D V Renouf, et al.Human Genetics|February 20, 2007
Enrichment of longevity phenotype in mtDNA haplogroups D4b2b, D4a, and D5 in the Japanese populationGabriela Alexe, Noriyuki Fuku, Erhan Bilal, et al.Human Genetics|February 9, 2007
Identification of 54 large deletions/duplications in TSC1 and TSC2 using MLPA, and genotype-phenotype correlationsPiotr Kozlowski, Penelope Roberts, Sandra Dabora, et al.Human Genetics|October 27, 2006
The possible role of 10398A and 16189C mtDNA variants in providing susceptibility to T2DM in two North Indian populations: a replicative studyAudesh Bhat, Anil Koul, Swarkar Sharma, et al.Human Genetics|November 1, 2006
A novel locus for maternally inherited human gingival fibromatosis at chromosome 11p15Yufei Zhu, Wenxia Zhang, Zhenghao Huo, et al.Pageof 957