A novel missense mutation in a C2 domain ofOTOF results in autosomal recessive auditory neuropathy von Tekin, Mustafa, Akcayoz, Duygu, Incesulu, Armagan

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A novel missense mutation in a C2 domain of OTOF results in autosomal recessive auditory neuropathy von Tekin, Mustafa, Akcayoz, Duygu, Incesulu, Armagan

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Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndrome von Ergür, Ayça T., Öcal, Gönül, Berberoglu, Merih, Tekin, Mustafa, Kiliç, Birim G., Aycan, Zehra, Kutlu, Alev, Adiyaman, Pelin, Sıklar, Zeynep, Akar, Nejat, Sahin, Aynur, Akçayöz, Duygu

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The c.IVS1+1G>A mutation intheGJB2 gene is prevalent and large deletions involving theGJB6 gene are not present in the Turkish population von Sirmaci, Asli, Akcayoz-Duman, Duygu, Tekin, Mustafa

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The c.IVS1+1G>A mutation in the GJB2 gene is prevalent and large deletions involving the GJB6 gene are not present in the Turkish population von Sirmaci, Asli, Akcayoz-Duman, Duygu, Tekin, Mustafa

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657del5 Mutation of the Nijmegen Breakage Syndrome Gene (NBS1) in the Turkish Population von TEKIN, MUSTAFA, AKCAYOZ, DUYGU, UCAR, CANAN, GULEN, HUSEYIN, AKAR, NEJAT

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