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1دورية أكاديمية
المؤلفون: Manzoli, Gabrielle N., Abe-Sandes, Kiyoko, Bittles, Alan H, da Silva, Danniel, Fernandes, Luciene, Paulon, Roberta, de Castro, Iza Cristina, Padovani, Carla, Acosta, Angelina
المصدر: Research outputs 2013
مصطلحات موضوعية: C.35delG, Connexin, Consanguinity, GJB2, Nonsyndromic hearing impairment, P.Arg75 Gln connexin 26, connexin 30, adolescent, adult, article, Brazil, child, ethnicity, familial disease, female, gene, gene mutation, genetic heterogeneity, GJB2 gene, GJB6 gene, hearing impairment, heterozygote, homozygote, human, major clinical study, male, MTRNR1 gene, preschool child, priority journal, school child
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2دورية أكاديمية
المؤلفون: Manzoli, Gabrielle N., Abe-Sandes, Kiyoko, Bittles, Alan H, da Silva, Danniel, Fernandes, Luciene, Paulon, Roberta, de Castro, Iza Cristina, Padovani, Carla, Acosta, Angelina
المصدر: Research outputs 2013
مصطلحات موضوعية: C.35delG, Connexin, Consanguinity, GJB2, Nonsyndromic hearing impairment, P.Arg75 Gln connexin 26, connexin 30, adolescent, adult, article, Brazil, child, ethnicity, familial disease, female, gene, gene mutation, genetic heterogeneity, GJB2 gene, GJB6 gene, hearing impairment, heterozygote, homozygote, human, major clinical study, male, MTRNR1 gene, preschool child, priority journal, school child
العلاقة: https://ro.ecu.edu.au/ecuworks2013/73Test; http://dx.doi.org/10.1016/j.ijporl.2013.04.001Test