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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

418 related items for PubMed ID: 31835641

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  • 2. Novel Mutations in CLPP, LARS2, CDH23, and COL4A5 Identified in Familial Cases of Prelingual Hearing Loss.
    Zafar S, Shahzad M, Ishaq R, Yousaf A, Shaikh RS, Akram J, Ahmed ZM, Riazuddin S.
    Genes (Basel); 2020 Aug 22; 11(9):. PubMed ID: 32842620
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  • 5. Homozygous mutations in Pakistani consanguineous families with prelingual nonsyndromic hearing loss.
    Park HR, Kanwal S, Lim SO, Nam DE, Choi YJ, Chung KW.
    Mol Biol Rep; 2020 Dec 22; 47(12):9979-9985. PubMed ID: 33269433
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  • 8. Identification and Computational Analysis of Rare Variants of Known Hearing Loss Genes Present in Five Deaf Members of a Pakistani Kindred.
    Saleem IB, Masoud MS, Qasim M, Ali M, Ahmed ZM.
    Genes (Basel); 2021 Nov 30; 12(12):. PubMed ID: 34946889
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  • 10. A novel mutation of TMPRSS3 related to milder auditory phenotype in Korean postlingual deafness: a possible future implication for a personalized auditory rehabilitation.
    Chung J, Park SM, Chang SO, Chung T, Lee KY, Kim AR, Park JH, Kim V, Park WY, Oh SH, Kim D, Park WJ, Choi BY.
    J Mol Med (Berl); 2014 Jun 30; 92(6):651-63. PubMed ID: 24526180
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  • 12. Whole exome sequencing of six Chinese families with hereditary non-syndromic hearing loss.
    Liang P, Chen F, Wang S, Li Q, Li W, Wang J, Chen J, Zha D.
    Int J Pediatr Otorhinolaryngol; 2021 Sep 30; 148():110817. PubMed ID: 34265623
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  • 17. Whole exome sequencing identifies novel compound heterozygous pathogenic variants in the MYO15A gene leading to autosomal recessive non-syndromic hearing loss.
    Sarmadi A, Nasrniya S, Narrei S, Nouri Z, Abtahi H, Tabatabaiefar MA.
    Mol Biol Rep; 2020 Jul 30; 47(7):5355-5364. PubMed ID: 32623615
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  • 18. Identification and computational analysis of USH1C, and SLC26A4 variants in Pakistani families with prelingual hearing loss.
    Noman M, Bukhari SA, Rehman S, Qasim M, Ali M, Riazuddin S, Ahmed ZM.
    Mol Biol Rep; 2020 Dec 30; 47(12):9987-9993. PubMed ID: 33231815
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  • 20. Molecular genetic landscape of hereditary hearing loss in Pakistan.
    Naz S.
    Hum Genet; 2022 Apr 30; 141(3-4):633-648. PubMed ID: 34308486
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