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Journal of Medical Genetics|November 7, 2006
Molecular and clinical characterisation of three Spanish families with maternally inherited non-syndromic hearing loss caused by the 1494C->T mutation in the mitochondrial 12S rRNA geneM Rodríguez-Ballesteros, M Olarte, L A Aguirre, et al.The Journal of Parasitology|July 24, 2004
Host gender in parasitic infections of mammals: an evaluation of the female host supremacy paradigmJ Morales-Montor, A Chavarria, M A De León, et al.Nature Genetics|November 1, 2001
Mutations in a new gene encoding a protein of the hair bundle cause non-syndromic deafness at the DFNB16 locusE Verpy, S Masmoudi, I Zwaenepoel, et al.American Journal of Human Genetics|October 16, 1999
The A1555G mutation in the 12S rRNA gene of human mtDNA: recurrent origins and founder events in families affected by sensorineural deafnessA Torroni, F Cruciani, C Rengo, et al.Journal of Medical Genetics|February 27, 2004
A genotype-phenotype correlation for GJB2 (connexin 26) deafnessK Cryns, E Orzan, A Murgia, et al.Clinical Genetics|March 19, 2010
A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expressionE Wilch, H Azaiez, R A Fisher, et al.Pageof 4