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Human Mutation|November 26, 1999
Novel mutation in the KCNQ4 gene in a large kindred with dominant progressive hearing lossZ Talebizadeh, P M Kelley, J W Askew, et al.Genomics|December 28, 1999
Human connexin 30 (GJB6), a candidate gene for nonsyndromic hearing loss: molecular cloning, tissue-specific expression, and assignment to chromosome 13q12P M Kelley, S Abe, J W Askew, et al.Plant Physiology|December 1, 1994
Differential induction of mRNAs for the glycolytic and ethanolic fermentative pathways by hypoxia and anoxia in maize seedlingsD L Andrews, D M MacAlpine, J R Johnson, et al.American Journal of Human Genetics|June 13, 1998
Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing lossP M Kelley, D J Harris, B C Comer, et al.Human Mutation|December 29, 1999
Erratum: analysis of DNA elements that modulate myosin VIIa expression in humansD J Orten, M D Weston, P M Kelley, et al.Human Mutation|September 30, 1999
Analysis of DNA elements that modulate myosin VIIA expression in humansD J Orten, M D Weston, P M Kelley, et al.Journal of Medical Genetics|April 4, 2000
Genetic heterogeneity of Usher syndrome type II: localisation to chromosome 5qS Pieke-Dahl, C G Möller, P M Kelley, et al.Journal of Learning Disabilities|October 27, 2004
Reading disability and chromosome 6p21.3: evaluation of MOG as a candidate geneS D Smith, P M Kelley, J W Askew, et al.Genomics|July 1, 1997
Isolation of a novel human homologue of the gene coding for echinoderm microtubule-associated protein (EMAP) from the Usher syndrome type 1a locus at 14q32J D Eudy, M Ma-Edmonds, S F Yao, et al.Genetic Testing|February 24, 2001
The M34T allele variant of connexin 26R A Cucci, S Prasad, P M Kelley, et al.Pageof 5