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Journal Abstract Search

286 related items for PubMed ID: 25491636

  • 21. A new autosomal recessive nonsyndromic hearing impairment locus DFNB96 on chromosome 1p36.31-p36.13.
    Ansar M, Lee K, Naqvi SK, Andrade PB, Basit S, Santos-Cortez RL, Ahmad W, Leal SM.
    J Hum Genet; 2011 Dec; 56(12):866-8. PubMed ID: 21937999
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  • 23. Genetic heterogeneity of congenital hearing impairment in Algerians from the Ghardaïa province.
    Talbi S, Bonnet C, Riahi Z, Boudjenah F, Dahmani M, Hardelin JP, Wong Jun Tai F, Louha M, Ammar-Khodja F, Petit C.
    Int J Pediatr Otorhinolaryngol; 2018 Sep; 112():1-5. PubMed ID: 30055715
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  • 24. Novel TMPRSS3 variants in Pakistani families with autosomal recessive non-syndromic hearing impairment.
    Lee K, Khan S, Islam A, Ansar M, Andrade PB, Kim S, Santos-Cortez RL, Ahmad W, Leal SM.
    Clin Genet; 2012 Jul; 82(1):56-63. PubMed ID: 21534946
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  • 32. Atypical patterns of segregation of familial enlargement of the vestibular aqueduct.
    Muskett JA, Chattaraj P, Heneghan JF, Reimold FR, Shmukler BE, Brewer CC, King KA, Zalewski CK, Shawker TH, Butman JA, Kenna MA, Chien WW, Alper SL, Griffith AJ.
    Laryngoscope; 2016 Jul; 126(7):E240-7. PubMed ID: 26485571
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  • 33. Localization of a novel autosomal recessive non-syndromic hearing impairment locus (DFNB38) to 6q26-q27 in a consanguineous kindred from Pakistan.
    Ansar M, Ramzan M, Pham TL, Yan K, Jamal SM, Haque S, Ahmad W, Leal SM.
    Hum Hered; 2003 Jul; 55(1):71-4. PubMed ID: 12890929
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  • 36. Novel OTOA mutations cause autosomal recessive non-syndromic hearing impairment in Pakistani families.
    Lee K, Chiu I, Santos-Cortez RL, Basit S, Khan S, Azeem Z, Andrade PB, Kim SS, Ahmad W, Leal SM.
    Clin Genet; 2013 Sep; 84(3):294-6. PubMed ID: 23173898
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  • 39. Homozygosity mapping identifies a novel GIPC3 mutation causing congenital nonsyndromic hearing loss in a Saudi family.
    Ramzan K, Al-Owain M, Allam R, Berhan A, Abuharb G, Taibah K, Imtiaz F.
    Gene; 2013 May 25; 521(1):195-9. PubMed ID: 23510777
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