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Journal of Human Genetics|December 16, 1998
Molecular diagnosis of patients with beta-thalassemia major in central Taiwan by amplified created restriction site analysisC T Peng, J Y Wu, C H Tsai, et al.Journal of Human Genetics|December 16, 1998
Further evidence for a major ancient mutation underlying myotonic dystrophy from linkage disequilibrium studies in the Japanese populationH Yamagata, M Nakagawa, K Johnson, et al.Journal of Human Genetics|December 16, 1998
Isolation and mapping of a novel human kidney- and liver-specific gene homologous to the bacterial acetyltransferasesK Ozaki, T Fujiwara, Y Nakamura, et al.Journal of Human Genetics|December 16, 1998
Novel missense mutation resulting in the substitution of tyrosine by cysteine at codon 597 of the type X collagen gene associated with Schmid metaphyseal chondrodysplasiaH Sawai, A Ida, Y Nakata, et al.Journal of Human Genetics|December 16, 1998
Cloning, expression analysis, and chromosomal localization of HIP1R, an isolog of huntingtin interacting protein (HIP1)N Seki, M Muramatsu, S Sugano, et al.Journal of Human Genetics|December 16, 1998
A HhaI/BstUI polymorphism in a novel gene at human chromosome 11p15.5K Miura, H Masuzaki, T Ishimaru, et al.Journal of Human Genetics|December 16, 1998
Isolation of a polymorphic CA repeat sequence at the human progesterone receptor (PGR) locusK Tsukamoto, I Watanabe, T Shiba, et al.Journal of Human Genetics|February 3, 2006
Molecular insights into the origins of the Shompen, a declining population of the Nicobar archipelagoRajni Trivedi, T Sitalaximi, Jheelam Banerjee, et al.Journal of Human Genetics|February 3, 2006
Biochemical data in ornithine transcarbamylase deficiency (OTCD) carrier risk estimation: logistic discrimination and combination with genetic informationKonrad OexleJournal of Human Genetics|February 8, 2006
A rapid and reliable detection system for the analysis of PMP22 gene dosage by MP/DHPLC assayChia-Yun Lin, Yi-Ning Su, Chien-Nan Lee, et al.Pageof 352