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Global genetic insight contributed by consanguineous Pakistani families segregating hearing loss.
Richard, Elodie M; Santos-Cortez, Regie Lyn P; Faridi, Rabia; Rehman, Atteeq U; Lee, Kwanghyuk; Shahzad, Mohsin; Acharya, Anushree; Khan, Asma A; Imtiaz, Ayesha; Chakchouk, Imen; Takla, Christina; Abbe, Izoduwa; Rafeeq, Maria; Liaqat, Khurram; Chaudhry, Taimur; Bamshad, Michael J; Nickerson, Deborah A; Schrauwen, Isabelle; Khan, Shaheen N; Morell, Robert J; Zafar, Saba; Ansar, Muhammad; Ahmed, Zubair M; Ahmad, Wasim; Riazuddin, Sheikh; Friedman, Thomas B; Leal, Suzanne M; Riazuddin, Saima.
Afiliación
  • Richard EM; Department of Otorhinolaryngology-Head and Neck Surgery, School of Medicine, University of Maryland, Baltimore, Maryland.
  • Santos-Cortez RLP; Center for Statistical Genetics, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Faridi R; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland.
  • Rehman AU; National Center for Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.
  • Lee K; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland.
  • Shahzad M; Center for Statistical Genetics, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Acharya A; Department of Otorhinolaryngology-Head and Neck Surgery, School of Medicine, University of Maryland, Baltimore, Maryland.
  • Khan AA; Pakistan Institute of Medical Sciences, Shaheed Zulfiqar Ali Bhutto Medical University, Islamabad, Pakistan.
  • Imtiaz A; Center for Statistical Genetics, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Chakchouk I; National Center for Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.
  • Takla C; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland.
  • Abbe I; Center for Statistical Genetics, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Rafeeq M; Laboratory of Molecular Genetics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland.
  • Liaqat K; Center for Statistical Genetics, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Chaudhry T; National Center for Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.
  • Bamshad MJ; Center for Statistical Genetics, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Nickerson DA; Department of Biotechnology, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
  • Schrauwen I; Department of Genome Sciences, University of Washington, Seattle, Washington.
  • Khan SN; Department of Genome Sciences, University of Washington, Seattle, Washington.
  • Zafar S; Center for Statistical Genetics, Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Ansar M; National Center for Excellence in Molecular Biology, University of the Punjab, Lahore, Pakistan.
  • Ahmed ZM; The Genomics and Computational Biology Core, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, Maryland.
  • Ahmad W; Institute of Molecular Biology and Biotechnology, Bahauddin Zakariya University, Multan, Pakistan.
  • Riazuddin S; Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
  • Friedman TB; Department of Otorhinolaryngology-Head and Neck Surgery, School of Medicine, University of Maryland, Baltimore, Maryland.
  • Leal SM; Department of Biochemistry, Faculty of Biological Sciences, Quaid-i-Azam University, Islamabad, Pakistan.
  • Riazuddin S; Pakistan Institute of Medical Sciences, Shaheed Zulfiqar Ali Bhutto Medical University, Islamabad, Pakistan.
Hum Mutat ; 40(1): 53-72, 2019 01.
Article en En | MEDLINE | ID: mdl-30303587
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Consanguinidad / Segregación Cromosómica / Pérdida Auditiva Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos
Texto completo
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XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Consanguinidad / Segregación Cromosómica / Pérdida Auditiva Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male País/Región como asunto: Asia Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2019 Tipo del documento: Article Pais de publicación: Estados Unidos