نتائج البحث - Ramzan, Memoona

Bi-allelic Pro291Leu variant in KCNQ4 leads to early onset non-syndromic hearing loss حسب Ramzan, Memoona, Idrees, Hafiza, Mujtaba, Ghulam, Sobreira, Nara, Witmer, P. Dane, Naz, Sadaf

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

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Genetic causes of moderate to severe hearing loss point to modifiers حسب Naz, Sadaf, Imtiaz, Ayesha, Mujtaba, Ghulam, Maqsood, Azra, Bashir, Rasheeda, Bukhari, Ihtisham, Khan, Muhammad R., Ramzan, Memoona, Fatima, Amara, Rehman, Atteeq U., Iqbal, Muddassar, Chaudhry, Taimur, Lund, Merete, Brewer, Carmen C., Morell, Robert J., Friedman, Thomas B.

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Variants of human CLDN9 cause mild to profound hearing loss حسب 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

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