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Genetic Testing of Non-familial Deaf Patients for CIB2 and GJB2 Mutations: Phenotype and Genetic Counselling.
Shaikh, Hina; Waryah, Ali M; Narsani, Ashok K; Iqbal, Muhammad; Shahzad, Mohsin; Waryah, Yar M; Shaikh, Naila; Mahmood, Amber.
Afiliação
  • Shaikh H; Molecular Biology and Genetics Department, Medical Research Center, Liaquat University of Medical and Health Sciences, Jamshoro, Pakistan.
  • Waryah AM; Molecular Biology and Genetics Department, Medical Research Center, Liaquat University of Medical and Health Sciences, Jamshoro, Pakistan. aliwaryah@lumhs.edu.pk.
  • Narsani AK; Institute of Ophthalmology, Liaquat University of Medical and Health Sciences, Jamshoro, Pakistan.
  • Iqbal M; Department of Biochemistry and Biotechnology, Islamia University, Bahawalpur, Pakistan.
  • Shahzad M; Department of Molecular Biology, Shaheed Zulfiqar Ali Bhutto Medical University, Islamabad, Pakistan.
  • Waryah YM; Molecular Biology and Genetics Department, Medical Research Center, Liaquat University of Medical and Health Sciences, Jamshoro, Pakistan.
  • Shaikh N; Molecular Biology and Genetics Department, Medical Research Center, Liaquat University of Medical and Health Sciences, Jamshoro, Pakistan.
  • Mahmood A; Molecular Biology and Genetics Department, Medical Research Center, Liaquat University of Medical and Health Sciences, Jamshoro, Pakistan.
Biochem Genet ; 55(5-6): 410-420, 2017 Dec.
Article em En | MEDLINE | ID: mdl-29086887
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Proteínas de Ligação ao Cálcio / Testes Genéticos / Conexinas / Surdez / Doenças Genéticas Inatas / Mutação Limite: Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Biochem Genet Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Paquistão
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Proteínas de Ligação ao Cálcio / Testes Genéticos / Conexinas / Surdez / Doenças Genéticas Inatas / Mutação Limite: Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Biochem Genet Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Paquistão