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Clinical Genetics|March 23, 2004
Cryptic chromosomal rearrangement screening in 30 patients with mental retardation and dysmorphic featuresL Rodriguez-Revenga, C Badenas, A Sánchez, et al.Clinical Genetics|March 23, 2004
Refining the primary open-angle glaucoma GLC1C region on chromosome 3 by haplotype analysisJ R Samples, G Kitsos, E Economou-Petersen, et al.Clinical Genetics|March 1, 1992
A new chromosome 9 variant: an extra band within the 9qh regionJ J HooClinical Genetics|December 25, 2004
Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non-syndromic hearing impairmentR L P Santos, M Wajid, T L Pham, et al.Clinical Genetics|December 25, 2004
Maternal mutation 677C > T in the methylenetetrahydrofolate reductase gene associated with severe brain injury in offspringR Dodelson de Kremer, C GrossoClinical Genetics|October 14, 2004
Exploration of the impact of messages about genes and race on lay attitudesC M Condit, R L Parrott, B R Bates, et al.Clinical Genetics|October 14, 2004
A_16_C haplotype in the FcepsilonRIbeta gene confers a higher risk for atopic asthma in the Indian populationS Sharma, R Nagarkatti, C B-Rao, et al.Clinical Genetics|October 14, 2004
High prevalence of V37I genetic variant in the connexin-26 (GJB2) gene among non-syndromic hearing-impaired and control Thai individualsD Wattanasirichaigoon, C Limwongse, C Jariengprasert, et al.Pageof 718