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Clinical Genetics|August 20, 2010
Desmin-related myopathyK Y van Spaendonck-Zwarts, L van Hessem, J D H Jongbloed, et al.Clinical Genetics|August 20, 2010
Association of polymorphisms in 9p21 region with CAD in North Indian population: replication of SNPs identified through GWASJ Kumar, S Yumnam, T Basu, et al.Clinical Genetics|September 16, 2010
Haplotype analysis of two recurrent genomic rearrangements in the BRCA1 gene suggests they are founder mutations for the Greek populationM Pertesi, I Konstantopoulou, D YannoukakosClinical Genetics|June 20, 2008
Genetic variations in the leptin and leptin receptor genes are associated with type 2 diabetes mellitus and metabolic traits in the Korean female populationH R Han, H-J Ryu, H S Cha, et al.Clinical Genetics|June 21, 2008
RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disordersF Brancati, L Travaglini, D Zablocka, et al.Clinical Genetics|October 8, 2009
Identification and functional analysis of novel mutations of the CLCNKB gene in Chinese patients with classic Bartter syndromeY Yu, C Xu, X Pan, et al.Clinical Genetics|October 8, 2009
The ryanodine receptor type 1 gene variants in African American men with exertional rhabdomyolysis and malignant hyperthermia susceptibilityN Sambuughin, J Capacchione, A Blokhin, et al.Clinical Genetics|February 14, 2009
Clinical and molecular diagnosis of the skeletal dysplasias associated with mutations in the gene encoding Fibroblast Growth Factor Receptor 3 (FGFR3) in PortugalM R Almeida, A B Campos-Xavier, A Medeira, et al.Clinical Genetics|March 1, 1991
Screening for fra(x) mutation and Klinefelter syndrome in mental institutionsV Pecile, G FilippiClinical Genetics|March 1, 1991
Hereditary hemorrhagic telangiectasia: report of 15 affected cases in a Mexican familyB Guillén, J Guízar, J de la Cruz, et al.Pageof 718