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Journal of Medical Genetics|May 1, 1995
Oguchi disease: suggestion of linkage to markers on chromosome 2qM A Maw, S John, S Jablonka, et al.Journal of Medical Genetics|June 3, 1999
Connexin26 deafness in several interconnected familiesS A Wilcox, A H Osborn, D R Allen-Powell, et al.American Journal of Medical Genetics|February 5, 1998
Mitochondrial A7445G mutation in two pedigrees with palmoplantar keratoderma and deafnessK B Sevior, A Hatamochi, I A Stewart, et al.Molecular and Cellular Biology|September 19, 1998
The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expressionM X Guan, J A Enriquez, N Fischel-Ghodsian, et al.Nature|April 22, 1993
Relaxation of insulin-like growth factor II gene imprinting implicated in Wilms' tumourO Ogawa, M R Eccles, J Szeto, et al.American Journal of Human Genetics|September 1, 1995
The contribution of the DFNB1 locus to neurosensory deafness in a Caucasian populationM A Maw, D R Allen-Powell, R J Goodey, et al.Nature Genetics|November 5, 1997
Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosaM A Maw, B Kennedy, A Knight, et al.Cancer Research|June 1, 1992
A third Wilms' tumor locus on chromosome 16qM A Maw, P E Grundy, L J Millow, et al.Human Molecular Genetics|December 10, 1999
A frameshift mutation in prominin (mouse)-like 1 causes human retinal degenerationM A Maw, D Corbeil, J Koch, et al.Human Molecular Genetics|October 23, 1997
Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 geneF Denoyelle, D Weil, M A Maw, et al.Pageof 1