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Journal of Human Genetics|March 18, 2000
A novel missense mutation in the HMG box region of the SRY gene in a Japanese patient with an XY sex reversalK Okuhara, T Tajima, J Nakae, et al.Journal of Human Genetics|August 3, 1999
The ADD1 G460W polymorphism is not associated with variation in blood pressure in Canadian Oji-CreeC P Busch, S B Harris, A J Hanley, et al.Journal of Human Genetics|August 3, 1999
Germline mutations in the EXT1 and EXT2 genes in Korean patients with hereditary multiple exostosesK J Park, K H Shin, J L Ku, et al.Journal of Human Genetics|August 3, 1999
Genetic alterations in the JAG1 gene in Japanese patients with Alagille syndromeY Onouchi, H Kurahashi, H Tajiri, et al.Journal of Human Genetics|August 3, 1999
Identification of a novel single base-pair polymorphism in the glutamate dehydrogenase (GLUD1) geneJ Muroi, A Uematsu, T YorifujiJournal of Human Genetics|August 3, 1999
A new single-nucleotide polymorphism in the seventh component of complement (C7) geneM Nakagawa, I Yuasa, K Umetsu, et al.Journal of Human Genetics|November 26, 1999
Mutational analysis of TSC1 and TSC2 genes in Japanese patients with tuberous sclerosis complexH Zhang, E Nanba, T Yamamoto, et al.Journal of Human Genetics|November 26, 1999
Prader-Willi syndrome in a child with XYYA Honma, R Ishii, A Ito, et al.Journal of Human Genetics|November 26, 1999
A polymorphic CA repeat marker at the human 27-kD calbindin (CALB1) locusK Morishima, S Matsuura, H Tauchi, et al.Journal of Human Genetics|November 26, 1999
A common Ile796Val polymorphism of the human SREBP cleavage-activating protein (SCAP) geneK Iwaki, T Nakajima, N Ota, et al.Pageof 351