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Year | Number of Results |
---|---|
2002 | 1 |
2004 | 1 |
2008 | 1 |
2010 | 2 |
2024 | 0 |
PubMed for id: 237587
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Homozygosity mapping reveals mutations of GRXCR1 as a cause of autosomal-recessive nonsyndromic hearing impairment.
Am J Hum Genet. 2010 Feb 12;86(2):138-47. doi: 10.1016/j.ajhg.2009.12.017. Epub 2010 Feb 4.
Am J Hum Genet. 2010.
PMID: 20137778
Free PMC article.
Mutations in Grxcr1 are the basis for inner ear dysfunction in the pirouette mouse.
Odeh H, Hunker KL, Belyantseva IA, Azaiez H, Avenarius MR, Zheng L, Peters LM, Gagnon LH, Hagiwara N, Skynner MJ, Brilliant MH, Allen ND, Riazuddin S, Johnson KR, Raphael Y, Najmabadi H, Friedman TB, Bartles JR, Smith RJ, Kohrman DC.
Odeh H, et al.
Am J Hum Genet. 2010 Feb 12;86(2):148-60. doi: 10.1016/j.ajhg.2010.01.016. Epub 2010 Feb 4.
Am J Hum Genet. 2010.
PMID: 20137774
Free PMC article.
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An integrated genetic and functional analysis of the role of type II transmembrane serine proteases (TMPRSSs) in hearing loss.
Guipponi M, Toh MY, Tan J, Park D, Hanson K, Ballana E, Kwong D, Cannon PZ, Wu Q, Gout A, Delorenzi M, Speed TP, Smith RJ, Dahl HH, Petersen M, Teasdale RD, Estivill X, Park WJ, Scott HS.
Guipponi M, et al.
Hum Mutat. 2008 Jan;29(1):130-41. doi: 10.1002/humu.20617.
Hum Mutat. 2008.
PMID: 17918732
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Characterization of two transgene insertional mutations at pirouette, a mouse deafness locus.
Odeh H, Hagiwara N, Skynner M, Mitchem KL, Beyer LA, Allen ND, Brilliant MH, Lebart MC, Dolan DF, Raphael Y, Kohrman DC.
Odeh H, et al.
Audiol Neurootol. 2004 Sep-Oct;9(5):303-14. doi: 10.1159/000080701. Epub 2004 Sep 3.
Audiol Neurootol. 2004.
PMID: 15347914
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Chromosome location and characterization of the human nicotinic acetylcholine receptor subunit alpha (alpha) 9 (CHRNA9) gene.
Lustig LR, Peng H.
Lustig LR, et al.
Cytogenet Genome Res. 2002;98(2-3):154-9. doi: 10.1159/000069804.
Cytogenet Genome Res. 2002.
PMID: 12697997
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