Diagnostic Exome Sequencing to Elucidate the Genetic Basis of Likely Recessive Disorders in Consanguineous Families

  • Periklis Makrythanasis
    Department of Genetic Medicine and Development; University of Geneva; Geneva Switzerland
  • Mari Nelis
    Department of Genetic Medicine and Development; University of Geneva; Geneva Switzerland
  • Federico A. Santoni
    Department of Genetic Medicine and Development; University of Geneva; Geneva Switzerland
  • Michel Guipponi
    Service of Genetic Medicine; University Hospitals of Geneva; Geneva Switzerland
  • Anne Vannier
    Department of Genetic Medicine and Development; University of Geneva; Geneva Switzerland
  • Frédérique Béna
    Service of Genetic Medicine; University Hospitals of Geneva; Geneva Switzerland
  • Stefania Gimelli
    Service of Genetic Medicine; University Hospitals of Geneva; Geneva Switzerland
  • Elisavet Stathaki
    Service of Genetic Medicine; University Hospitals of Geneva; Geneva Switzerland
  • Samia Temtamy
    Department of Clinical Genetics; National Research Centre; Cairo Egypt
  • André Mégarbané
    Medical Genetics Unit; Saint Joseph University; Beirut Lebanon
  • Amira Masri
    Pediatric Department; The University of Jordan; Amman Jordan
  • Mona S. Aglan
    Department of Clinical Genetics; National Research Centre; Cairo Egypt
  • Maha S. Zaki
    Department of Clinical Genetics; National Research Centre; Cairo Egypt
  • Armand Bottani
    Service of Genetic Medicine; University Hospitals of Geneva; Geneva Switzerland
  • Siv Fokstuen
    Service of Genetic Medicine; University Hospitals of Geneva; Geneva Switzerland
  • Lorraine Gwanmesia
    Service of Genetic Medicine; University Hospitals of Geneva; Geneva Switzerland
  • Konstantinos Aliferis
    Service of Genetic Medicine; University Hospitals of Geneva; Geneva Switzerland
  • Mariana Bustamante Eduardo
    Department of Genetic Medicine and Development; University of Geneva; Geneva Switzerland
  • Georgios Stamoulis
    Department of Genetic Medicine and Development; University of Geneva; Geneva Switzerland
  • Stavroula Psoni
    Department of Medical Genetics; University of Athens; Athens Greece
  • Sofia Kitsiou-Tzeli
    Department of Medical Genetics; University of Athens; Athens Greece
  • Helen Fryssira
    Department of Medical Genetics; University of Athens; Athens Greece
  • Emmanouil Kanavakis
    Department of Medical Genetics; University of Athens; Athens Greece
  • Nasir Al-Allawi
    Department of Pathology, College of Medicine; University of Dohuk; Dohuk Iraq
  • Abdelaziz Sefiani
    Department of Medical Genetics; Institut National d'Hygiène; Rabat Morocco
  • Sana' Al Hait
    Genetics & IVF Department; The Farah Hospital; Amman Jordan
  • Siham C. Elalaoui
    Department of Medical Genetics; Institut National d'Hygiène; Rabat Morocco
  • Nadine Jalkh
    Medical Genetics Unit; Saint Joseph University; Beirut Lebanon
  • Lihadh Al-Gazali
    Department of Pediatrics, College of Medicine and Health Sciences; United Arab Emirates University; Al-Ain United Arab Emirates
  • Fatma Al-Jasmi
    Department of Pediatrics, College of Medicine and Health Sciences; United Arab Emirates University; Al-Ain United Arab Emirates
  • Habiba Chaabouni Bouhamed
    Department of Human Genetics, Faculty of Medicine; University Tunis El Manar; Tunis Tunisia
  • Ebtesam Abdalla
    Department of Human Genetics, Medical Research Institute; Alexandria University; Alexandria Egypt
  • David N. Cooper
    Institute of Medical Genetics, School of Medicine; Cardiff University; Cardiff UK
  • Hanan Hamamy
    Department of Genetic Medicine and Development; University of Geneva; Geneva Switzerland
  • Stylianos E. Antonarakis
    Department of Genetic Medicine and Development; University of Geneva; Geneva Switzerland

収録刊行物

  • Human Mutation

    Human Mutation 35 (10), 1203-1210, 2014-08-18

    Hindawi Limited

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