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Xq21.31–q21.32 duplication underlies intellectual disability in a large family with five affected males
Authors:Sulman Basit  Omhani I Malibari  Alia M Al‐Balawi  Sibtain Afzal  Amr Elsayed Mohamed Eldardear  Khushnooda Ramzan
Institution:1. Center for Genetics and Inherited Diseases, Taibah University Almadinah Almunawwarah, Saudi Arabia;2. Correspondence to:;3. Sulman Basit, Ph.D., Center for Genetics and Inherited Diseases, Taibah University Almadinah Almunawwarah, Kingdom of Saudi Arabia.;4. E‐mail:;5. Department of Metabolic Diseases, King Abdulla Medical City‐Madinah Maternity and Children Hospital, Almadinah Almunawwarah, Saudi Arabia;6. Prince Naif Centre for Immunology Research, College of Medicine, King Saud University, Riyadh, Saudi Arabia;7. College of Medicine, Taibah University Almadinah Almunawwarah, Saudi Arabia;8. Department of Genetics, Research Centre, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
Abstract:
Keywords:intellectual disability  x‐linked  copy number variation
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