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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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1998 | 1 |
2009 | 1 |
2013 | 1 |
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2019 | 1 |
2024 | 0 |
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SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis.
J Hum Genet. 2009 May;54(5):266-70. doi: 10.1038/jhg.2009.21. Epub 2009 Mar 13.
J Hum Genet. 2009.
PMID: 19287372
Molecular etiology of hearing impairment associated with nonsyndromic enlarged vestibular aqueduct in East China.
Chai Y, Huang Z, Tao Z, Li X, Li L, Li Y, Wu H, Yang T.
Chai Y, et al.
Am J Med Genet A. 2013 Sep;161A(9):2226-33. doi: 10.1002/ajmg.a.36068. Epub 2013 Aug 5.
Am J Med Genet A. 2013.
PMID: 23918157
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The Study of SLC26A4 Gene Causing Autosomal Recessive Hearing Loss by Linkage Analysis in a Cohort of Iranian Populations.
Reiisi S, Sanati MH, Tabatabaiefar MA, Ahmadian S, Reiisi S, Parchami S, Porjafari H, Shahi H, Shavarzi A, Hashemzade Chaleshtori M.
Reiisi S, et al.
Int J Mol Cell Med. 2014 Summer;3(3):176-82.
Int J Mol Cell Med. 2014.
PMID: 25317404
Free PMC article.
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Screening of 10 DFNB Loci Causing Autosomal Recessive Non-Syndromic Hearing Loss in Two Iranian Populations Negative for GJB2 Mutations.
Koohiyan M, Reiisi S, Azadegan-Dehkordi F, Salehi M, Abtahi H, Hashemzadeh-Chaleshtori M, Noori-Daloii MR, Tabatabaiefar MA.
Koohiyan M, et al.
Iran J Public Health. 2019 Sep;48(9):1704-1713.
Iran J Public Health. 2019.
PMID: 31700827
Free PMC article.
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Two frequent missense mutations in Pendred syndrome.
Van Hauwe P, Everett LA, Coucke P, Scott DA, Kraft ML, Ris-Stalpers C, Bolder C, Otten B, de Vijlder JJ, Dietrich NL, Ramesh A, Srisailapathy SC, Parving A, Cremers CW, Willems PJ, Smith RJ, Green ED, Van Camp G.
Van Hauwe P, et al.
Hum Mol Genet. 1998 Jul;7(7):1099-104. doi: 10.1093/hmg/7.7.1099.
Hum Mol Genet. 1998.
PMID: 9618166
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