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Clinical Genetics|June 25, 2010
Haplotype sharing test maps genes for familial cardiomyopathiesP A van der Zwaag, J P van Tintelen, F Gerbens, et al.Clinical Genetics|July 6, 2010
Testing for CHEK2 in the cancer genetics clinic: ready for prime time?S A NarodClinical Genetics|June 24, 2010
Identification of two novel mutations in Shh long-range regulator associated with familial pre-axial polydactylyJ Albuisson, B Isidor, M Giraud, et al.Clinical Genetics|May 22, 2010
High-resolution molecular karyotyping in patients with developmental delay and/or multiple congenital anomalies in a clinical settingJ Wincent, B-M Anderlid, M Lagerberg, et al.Clinical Genetics|April 1, 1991
Progressive encephalopathy with edema, hypsarrhythmia, and optic atrophy (PEHO syndrome)R Salonen, M Somer, M Haltia, et al.Clinical Genetics|April 1, 1991
Transcobalamins in the etiology of neural tube defectsP Magnus, E M Magnus, K BergClinical Genetics|August 5, 2010
Pseudoautosomal inheritance of Léri-Weill syndrome: what does it mean?C Evers, P H Heidemann, D Dunstheimer, et al.Clinical Genetics|August 5, 2010
Hippocampus development and function: role of epigenetic factors and implications for cognitive diseaseP S Lagali, C P Corcoran, D J PickettsClinical Genetics|August 20, 2010
Mutation screening of spastin, atlastin, and REEP1 in hereditary spastic paraplegiaD S McCorquodale, U Ozomaro, J Huang, et al.Pageof 718