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E R Wilcox

Showing results (21-30 of 28) with videos related to

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Nature Genetics|December 2, 2000
Dominant modifier DFNM1 suppresses recessive deafness DFNB26S Riazuddin, C M Castelein, Z M Ahmed, et al.
Genome Research|October 1, 1995
An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6K Fukushima, A Ramesh, C R Srisailapathy, et al.
Human Genetics|December 6, 2001
Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndromeN Liburd, M Ghosh, S Riazuddin, et al.
Cell|February 13, 2001
Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29E R Wilcox, Q L Burton, S Naz, et al.
Journal of Medical Genetics|April 5, 2003
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafnessH-J Park, S Shaukat, X-Z Liu, et al.
Human Genetics|July 8, 1998
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutationsA L DeStefano, L A Cupples, K S Arnos, et al.
American Journal of Human Genetics|June 13, 1998
Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2Y Liang, A Wang, F J Probst, et al.
American Journal of Human Genetics|November 25, 2000
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23J M Bork, L M Peters, S Riazuddin, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
Nature Genetics|December 2, 2000
Dominant modifier DFNM1 suppresses recessive deafness DFNB26S Riazuddin, C M Castelein, Z M Ahmed, et al.
Genome Research|October 1, 1995
An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6K Fukushima, A Ramesh, C R Srisailapathy, et al.
Human Genetics|December 6, 2001
Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndromeN Liburd, M Ghosh, S Riazuddin, et al.
Cell|February 13, 2001
Mutations in the gene encoding tight junction claudin-14 cause autosomal recessive deafness DFNB29E R Wilcox, Q L Burton, S Naz, et al.
Journal of Medical Genetics|April 5, 2003
Origins and frequencies of SLC26A4 (PDS) mutations in east and south Asians: global implications for the epidemiology of deafnessH-J Park, S Shaukat, X-Z Liu, et al.
Human Genetics|July 8, 1998
Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutationsA L DeStefano, L A Cupples, K S Arnos, et al.
American Journal of Human Genetics|June 13, 1998
Genetic mapping refines DFNB3 to 17p11.2, suggests multiple alleles of DFNB3, and supports homology to the mouse model shaker-2Y Liang, A Wang, F J Probst, et al.
American Journal of Human Genetics|November 25, 2000
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23J M Bork, L M Peters, S Riazuddin, et al.
Pageof 3