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Human Mutation|October 29, 2002
Molecular analysis in Japanese patients with Charcot-Marie-Tooth disease: DGGE analysis for PMP22, MPZ, and Cx32/GJB1 mutationsChikahiko Numakura, Changqing Lin, Tohru Ikegami, et al.Human Mutation|October 29, 2002
Clustering of variations and haplotype analysis in the highly variable region of exon 11 of BRCA1 in Chinese women with sporadic breast cancerYunqing Li, Sizhong Zhang, Cuiying Xiao, et al.Human Mutation|October 29, 2002
The LDL receptor-related protein (LRP1/A2MR) and coronary atherosclerosis--novel genomic variants and functional consequencesSusanne Schulz, Undraga Schagdarsurengin, Petra Greiser, et al.Human Mutation|November 21, 2002
SLC26A3 mutations in congenital chloride diarrheaSiru Mäkelä, Juha Kere, Christer Holmberg, et al.Human Mutation|November 21, 2002
Proposal for an allele nomenclature system based on the evolutionary divergence of haplotypesDaniel W NebertHuman Mutation|November 21, 2002
Novel mutations in the MYOC/GLC1A gene in a large group of glaucoma patientsKarin Michels-Rautenstrauss, Christian Mardin, Nina Wakili, et al.Human Mutation|November 21, 2002
Missense mutations in the extracellular domain of the human neural cell adhesion molecule L1 reduce neurite outgrowth of murine cerebellar neuronsPiret Michelson, Christine Hartwig, Melitta Schachner, et al.Human Mutation|July 19, 2002
RYR1 mutations causing central core disease are associated with more severe malignant hyperthermia in vitro contracture test phenotypesRachel L Robinson, Collin Brooks, Sarah L Brown, et al.Human Mutation|July 19, 2002
Identification of five novel WASP mutations in Chinese families with Wiskott-Aldrich syndromeKoon-Wing Chan, Tsz-Leung Lee, Brian Hon-Yin Chung, et al.Human Mutation|July 19, 2002
Mutations in the human ATP-binding cassette transporters ABCG5 and ABCG8 in sitosterolemiaSusanne Heimerl, Thomas Langmann, Christoph Moehle, et al.Pageof 577