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Journal Abstract Search

286 related items for PubMed ID: 25491636

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  • 9. Homozygosity mapping of autosomal recessive intellectual disability loci in 11 consanguineous Pakistani families.
    Ahmed I, Rafiq MA, Vincent JB, Bhatti A, Ayub M, John P.
    Acta Neuropsychiatr; 2015 Feb; 27(1):38-47. PubMed ID: 25434728
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  • 10. Genetics of Hearing Loss--Nonsyndromic.
    Chang KW.
    Otolaryngol Clin North Am; 2015 Dec; 48(6):1063-72. PubMed ID: 26275501
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  • 11. Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42.
    Borck G, Ur Rehman A, Lee K, Pogoda HM, Kakar N, von Ameln S, Grillet N, Hildebrand MS, Ahmed ZM, Nürnberg G, Ansar M, Basit S, Javed Q, Morell RJ, Nasreen N, Shearer AE, Ahmad A, Kahrizi K, Shaikh RS, Ali RA, Khan SN, Goebel I, Meyer NC, Kimberling WJ, Webster JA, Stephan DA, Schiller MR, Bahlo M, Najmabadi H, Gillespie PG, Nürnberg P, Wollnik B, Riazuddin S, Smith RJ, Ahmad W, Müller U, Hammerschmidt M, Friedman TB, Riazuddin S, Leal SM, Ahmad J, Kubisch C.
    Am J Hum Genet; 2011 Feb 11; 88(2):127-37. PubMed ID: 21255762
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  • 12. Delineation of Homozygous Variants Associated with Prelingual Sensorineural Hearing Loss in Pakistani Families.
    Noman M, Ishaq R, Bukhari SA, Ahmed ZM, Riazuddin S.
    Genes (Basel); 2019 Dec 10; 10(12):. PubMed ID: 31835641
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  • 13. Genetic Spectrum of Syndromic and Non-Syndromic Hearing Loss in Pakistani Families.
    Doll J, Vona B, Schnapp L, Rüschendorf F, Khan I, Khan S, Muhammad N, Alam Khan S, Nawaz H, Khan A, Ahmad N, Kolb SM, Kühlewein L, Labonne JDJ, Layman LC, Hofrichter MAH, Röder T, Dittrich M, Müller T, Graves TD, Kong IK, Nanda I, Kim HG, Haaf T.
    Genes (Basel); 2020 Nov 11; 11(11):. PubMed ID: 33187236
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  • 14. Mutations of GJB2 in three geographic isolates from northern Tunisia: evidence for genetic heterogeneity within isolates.
    Ben Arab S, Hmani M, Denoyelle F, Boulila-Elgaied A, Chardenoux S, Hachicha S, Petit C, Ayadi H.
    Clin Genet; 2000 Jun 11; 57(6):439-43. PubMed ID: 10905664
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  • 15. Genetic analysis through OtoSeq of Pakistani families segregating prelingual hearing loss.
    Shahzad M, Sivakumaran TA, Qaiser TA, Schultz JM, Hussain Z, Flanagan M, Bhinder MA, Kissell D, Greinwald JH, Khan SN, Friedman TB, Zhang K, Riazuddin S, Riazuddin S, Ahmed ZM.
    Otolaryngol Head Neck Surg; 2013 Sep 11; 149(3):478-87. PubMed ID: 23770805
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  • 16. A comprehensive introduction to the genetic basis of non-syndromic hearing loss in the Saudi Arabian population.
    Imtiaz F, Taibah K, Ramzan K, Bin-Khamis G, Kennedy S, Al-Mubarak B, Trabzuni D, Allam R, Al-Mostafa A, Sogaty S, Al-Shaikh AH, Bamukhayyar SS, Meyer BF, Al-Owain M.
    BMC Med Genet; 2011 Jul 04; 12():91. PubMed ID: 21726435
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  • 18. Genetic Causes of Oculocutaneous Albinism in Pakistani Population.
    Sajid Z, Yousaf S, Waryah YM, Mughal TA, Kausar T, Shahzad M, Rao AR, Abbasi AA, Shaikh RS, Waryah AM, Riazuddin S, Ahmed ZM.
    Genes (Basel); 2021 Mar 28; 12(4):. PubMed ID: 33800529
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