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| | 1 - 10 of 117 journal articles in the PubMed database | Email to a friend | | |
| Bramhall NF, Kallman JC, Verrall AM, et al.
A novel WFS1 mutation in a family with dominant low frequency sensorineural hearing loss with normal VEMP and EcochG findings. [JOURNAL ARTICLE]
BMC Med Genet 2008 Jun 2; 9(1):48.
Abstract | Full Citation | Find Related Articles | | Tsai HT, Wang YP, Chung SF, et al.
A novel mutation in the WFS1 gene identified in a Taiwanese family with low-frequency hearing impairment. [JOURNAL ARTICLE]
BMC Med Genet 2007 May 22; 8(1):26.
Abstract | Full Citation | Find Related Articles | | Noguchi Y, Yashima T, Hatanaka A, et al.
A mutation in Wolfram syndrome type 1 gene in a Japanese family with autosomal dominant low-frequency sensorineural hearing loss. [Journal Article]
Acta Otolaryngol 2005 Nov; 125(11):1189-94.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Bespalova IN, Van Camp G, Bom SJ, et al.
Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss. [Journal Article]
Hum Mol Genet 2001 Oct 15; 10(22):2501-8.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Fukuoka H, Kanda Y, Ohta S, et al.
Mutations in the WFS1 gene are a frequent cause of autosomal dominant nonsyndromic low-frequency hearing loss in Japanese. [JOURNAL ARTICLE]
J Hum Genet 2007 May 11.
Abstract | Full Citation | Find Related Articles | | Lesperance MM, Hall JW, San Agustin TB, et al.
Mutations in the Wolfram syndrome type 1 gene (WFS1) define a clinical entity of dominant low-frequency sensorineural hearing loss. [Journal Article]
Arch Otolaryngol Head Neck Surg 2003 Apr; 129(4):411-20.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Komatsu K, Nakamura N, Ghadami M, et al.
Confirmation of genetic homogeneity of nonsyndromic low-frequency sensorineural hearing loss by linkage analysis and a DFNA6/14 mutation in a Japanese family. [Case Reports, Journal Article, Research Support, Non-U.S. Gov't ]
J Hum Genet 2002; 47(8):395-9.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Eiberg H, Hansen L, Kjer B, et al.
Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 gene. [Journal Article]
J Med Genet 2006 May; 43(5):435-40.
Abstract | Full Citation | Publisher Full Text | Find Related Articles | | Sivakumaran TA, Lesperance MM
A PCR-RFLP assay for the A716T mutation in the WFS1 gene, a common cause of low-frequency sensorineural hearing loss. [Journal Article]
Genet Test 2002; 6(3):229-31.
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