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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1995 | 1 |
1996 | 1 |
1997 | 1 |
2002 | 2 |
2024 | 0 |
PubMed (OMIM) for id: 322084
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Beethoven, a mouse model for dominant, progressive hearing loss DFNA36.
Nat Genet. 2002 Mar;30(3):257-8. doi: 10.1038/ng848. Epub 2002 Feb 19.
Nat Genet. 2002.
PMID: 11850623
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Kurima K, Peters LM, Yang Y, Riazuddin S, Ahmed ZM, Naz S, Arnaud D, Drury S, Mo J, Makishima T, Ghosh M, Menon PS, Deshmukh D, Oddoux C, Ostrer H, Khan S, Riazuddin S, Deininger PL, Hampton LL, Sullivan SL, Battey JF Jr, Keats BJ, Wilcox ER, Friedman TB, Griffith AJ.
Kurima K, et al.
Nat Genet. 2002 Mar;30(3):277-84. doi: 10.1038/ng842. Epub 2002 Feb 19.
Nat Genet. 2002.
PMID: 11850618
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Nonsyndromic hearing impairment: unparalleled heterogeneity.
Van Camp G, Willems PJ, Smith RJ.
Van Camp G, et al.
Am J Hum Genet. 1997 Apr;60(4):758-64.
Am J Hum Genet. 1997.
PMID: 9106521
Free PMC article.
Review.
No abstract available.
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An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindreds.
Scott DA, Carmi R, Elbedour K, Yosefsberg S, Stone EM, Sheffield VC.
Scott DA, et al.
Am J Hum Genet. 1996 Aug;59(2):385-91.
Am J Hum Genet. 1996.
PMID: 8755925
Free PMC article.
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A human recessive neurosensory nonsyndromic hearing impairment locus is potential homologue of murine deafness (dn) locus.
Jain PK, Fukushima K, Deshmukh D, Ramesh A, Thomas E, Lalwani AK, Kumar S, Plopis B, Skarka H, Srisailapathy CR, et al.
Jain PK, et al.
Hum Mol Genet. 1995 Dec;4(12):2391-4. doi: 10.1093/hmg/4.12.2391.
Hum Mol Genet. 1995.
PMID: 8634715
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