檢索結果 - Salman, Midhat

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    Mutations of GJB2 Encoding Connexin 26 Contribute to Nonsyndromic Moderate and Severe Hearing Loss in Pakistan

    Mutations of GJB2 Encoding Connexin 26 Contribute to Nonsyndromic Moderate and Severe Hearing Loss in Pakistan 由 Salman, Midhat, Bashir, Rasheeda, Imtiaz, Ayesha, Maqsood, Azra, Mujtaba, Ghulam, Iqbal, Muddassar, Naz, Sadaf

    出版 2015
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    Spectrum of genetic variants in moderate to severe sporadic hearing loss in Pakistan

    Spectrum of genetic variants in moderate to severe sporadic hearing loss in Pakistan 由 Ramzan, Memoona, Bashir, Rasheeda, Salman, Midhat, Mujtaba, Ghulam, Sobreira, Nara, Witmer, P. Dane, Naz, Sadaf

    出版 2020
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    Variants of human CLDN9 cause mild to profound hearing loss

    Variants of human CLDN9 cause mild to profound hearing loss 由 Ramzan, Memoona, Philippe, Christophe, Belyantseva, Inna A., Nakano, Yoko, Fenollar-Ferrer, Cristina, Tona, Risa, Yousaf, Rizwan, Basheer, Rasheeda, Imtiaz, Ayesha, Faridi, Rabia, Munir, Zunaira, Idrees, Hafiza, Salman, Midhat, Nambot, Sophie, Vitobello, Antonio, Kartti, Souad, Zarrik, Oumaima, Witmer, P. Dane, Sobreria, Nara, Ibrahimi, Azeddine, Banfi, Botond, Moutton, Sebastien, Friedman, Thomas B., Naz, Sadaf

    出版 2021
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