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Year | Number of Results |
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1995 | 1 |
1996 | 2 |
2002 | 2 |
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PubMed (cited) for id: 600971
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Page 1
A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia.
Clin Genet. 2009 Jun;75(6):562-7. doi: 10.1111/j.1399-0004.2009.01183.x. Epub 2009 May 5.
Clin Genet. 2009.
PMID: 19438934
Mutations in a novel gene, TMIE, are associated with hearing loss linked to the DFNB6 locus.
Naz S, Giguere CM, Kohrman DC, Mitchem KL, Riazuddin S, Morell RJ, Ramesh A, Srisailpathy S, Deshmukh D, Riazuddin S, Griffith AJ, Friedman TB, Smith RJ, Wilcox ER.
Naz S, et al.
Am J Hum Genet. 2002 Sep;71(3):632-6. doi: 10.1086/342193. Epub 2002 Jul 24.
Am J Hum Genet. 2002.
PMID: 12145746
Free PMC article.
Item in Clipboard
Mutation of the novel gene Tmie results in sensory cell defects in the inner ear of spinner, a mouse model of human hearing loss DFNB6.
Mitchem KL, Hibbard E, Beyer LA, Bosom K, Dootz GA, Dolan DF, Johnson KR, Raphael Y, Kohrman DC.
Mitchem KL, et al.
Hum Mol Genet. 2002 Aug 1;11(16):1887-98. doi: 10.1093/hmg/11.16.1887.
Hum Mol Genet. 2002.
PMID: 12140191
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Genes responsible for human hereditary deafness: symphony of a thousand.
Petit C.
Petit C.
Nat Genet. 1996 Dec;14(4):385-91. doi: 10.1038/ng1296-385.
Nat Genet. 1996.
PMID: 8944017
Review.
Item in Clipboard
A gene responsible for a sensorineural nonsyndromic recessive deafness maps to chromosome 2p22-23.
Chaïb H, Place C, Salem N, Chardenoux S, Vincent C, Weissenbach J, El-Zir E, Loiselet J, Petit C.
Chaïb H, et al.
Hum Mol Genet. 1996 Jan;5(1):155-8. doi: 10.1093/hmg/5.1.155.
Hum Mol Genet. 1996.
PMID: 8789454
Item in Clipboard
An autosomal recessive nonsyndromic form of sensorineural hearing loss maps to 3p-DFNB6.
Fukushima K, Ramesh A, Srisailapathy CR, Ni L, Wayne S, O'Neill ME, Van Camp G, Coucke P, Jain P, Wilcox ER, Smith SD, Kenyon JB, Zbar RI, Smith RJ.
Fukushima K, et al.
Genome Res. 1995 Oct;5(3):305-8. doi: 10.1101/gr.5.3.305.
Genome Res. 1995.
PMID: 8593615
Free article.
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