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A J Griffith

Showing results (31-40 of 41) with videos related to

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Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 1, 1996
Location of the 9257 and ataxia mutations on mouse chromosome 18A J Griffith, G L Radice, D L Burgess, et al.
Journal of Medical Genetics|July 7, 2009
Segregation of enlarged vestibular aqueducts in families with non-diagnostic SLC26A4 genotypesB Y Choi, A C Madeo, K A King, et al.
Journal of Medical Genetics|February 4, 2005
SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entitiesS P Pryor, A C Madeo, J C Reynolds, et al.
Journal of Medical Genetics|October 22, 2003
Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type IIIS L Ness, T Ben-Yosef, A Bar-Lev, et al.
Nature Genetics|December 2, 2000
Dominant modifier DFNM1 suppresses recessive deafness DFNB26S Riazuddin, C M Castelein, Z M Ahmed, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 15, 2001
Auditory dysfunction in Stickler syndromeY M Szymko-Bennett, M A Mastroianni, L I Shotland, 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.
Clinical Genetics|February 1, 2005
Genetic basis of hearing loss associated with enlarged vestibular aqueducts in KoreansH-J Park, S-J Lee, H-S Jin, 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.
Nature Genetics|December 2, 1999
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)W T McGuirt, S D Prasad, A J Griffith, et al.
Pageof 5

Showing results (31-40 of 41) with videos related to

Sort By:
Pageof 5
Mammalian Genome : Official Journal of the International Mammalian Genome Society|June 1, 1996
Location of the 9257 and ataxia mutations on mouse chromosome 18A J Griffith, G L Radice, D L Burgess, et al.
Journal of Medical Genetics|July 7, 2009
Segregation of enlarged vestibular aqueducts in families with non-diagnostic SLC26A4 genotypesB Y Choi, A C Madeo, K A King, et al.
Journal of Medical Genetics|February 4, 2005
SLC26A4/PDS genotype-phenotype correlation in hearing loss with enlargement of the vestibular aqueduct (EVA): evidence that Pendred syndrome and non-syndromic EVA are distinct clinical and genetic entitiesS P Pryor, A C Madeo, J C Reynolds, et al.
Journal of Medical Genetics|October 22, 2003
Genetic homogeneity and phenotypic variability among Ashkenazi Jews with Usher syndrome type IIIS L Ness, T Ben-Yosef, A Bar-Lev, et al.
Nature Genetics|December 2, 2000
Dominant modifier DFNM1 suppresses recessive deafness DFNB26S Riazuddin, C M Castelein, Z M Ahmed, et al.
Archives of Otolaryngology--Head & Neck Surgery|September 15, 2001
Auditory dysfunction in Stickler syndromeY M Szymko-Bennett, M A Mastroianni, L I Shotland, 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.
Clinical Genetics|February 1, 2005
Genetic basis of hearing loss associated with enlarged vestibular aqueducts in KoreansH-J Park, S-J Lee, H-S Jin, 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.
Nature Genetics|December 2, 1999
Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13)W T McGuirt, S D Prasad, A J Griffith, et al.
Pageof 5