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Journal of Human Genetics|March 25, 2006
COL7A1 mutation G2037E causes epidermal retention of type VII collagenDaisuke Sawamura, Kazuko Sato-Matsumura, Satoko Shibata, et al.Journal of Human Genetics|December 16, 1998
Anticipation in Japanese families with schizophreniaA Imamura, S Honda, Y Nakane, et al.Journal of Human Genetics|December 16, 1998
New dominant syndrome of microcephaly, facial abnormalities, micromelia, and mental retardationM Tsukahara, Y SugioJournal of Human Genetics|December 16, 1998
Mutation analysis of the phenylalanine hydroxylase gene and its clinical implications in two Japanese patients with non-phenylketonuria hyperphenylalaninemiaM Kibayashi, M Nagao, S ChibaJournal of Human Genetics|December 16, 1998
Isolation, tissue expression, and chromosomal assignment of a novel human gene which encodes a protein with RING finger motifN Seki, A Hattori, S Sugano, et al.Journal of Human Genetics|December 16, 1998
Chromosomal assignment of the gene for human DNA-PKcs interacting protein (KIP) on chromosome 15q25.3-q26.1 by somatic hybrid analysis and fluorescence in situ hybridizationN Seki, A Hayashi, M Abe, et al.Journal of Human Genetics|December 16, 1998
A highly polymorphic CA repeat marker at the human tumor necrosis factor alpha (TNFA alpha) locusK Tsukamoto, N Ohta, Y Shirai, et al.Journal of Human Genetics|December 15, 2007
Austronesian genetic signature in East African Madagascar and PolynesiaM Regueiro, S Mirabal, H Lacau, et al.Journal of Human Genetics|May 27, 2008
Does increased nuchal translucency indicate a fetal abnormality? A retrospective study to clarify the clinical significance of nuchal translucency in JapanShigo Yoshida, Kiyonori Miura, Kentaro Yamasaki, et al.Journal of Human Genetics|January 17, 2025
Returning genetic risk information for hereditary cancers to participants in a population-based cohort study in JapanKinuko Ohneda, Yoichi Suzuki, Yohei Hamanaka, et al.Pageof 351