Molecular Diagnosis of Fragile X Syndrome in Subjects with Intellectual Disability of Unknown Origin: Implications of Its Prevalence in Regional Pakistan

• Madiha Kanwal,

  Affiliation Human Genetics Program, Department of Animal Sciences, Quaid-i-Azam University Islamabad, 45320 Islamabad, Pakistan

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• Saadia Alyas,

  Affiliation Human Genetics Program, Department of Animal Sciences, Quaid-i-Azam University Islamabad, 45320 Islamabad, Pakistan

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• Muhammad Afzal,

  Affiliation Human Genetics Program, Department of Animal Sciences, Quaid-i-Azam University Islamabad, 45320 Islamabad, Pakistan

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• Atika Mansoor,

  Affiliation Institute of Biomedical and Genetic Engineering, Islamabad, Pakistan

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• Rashda Abbasi,

  Affiliation Institute of Biomedical and Genetic Engineering, Islamabad, Pakistan

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• Flora Tassone,

  Affiliations M.I.N.D. Institute, University of California Davis, Davis, California, United States of America, Department of Biochemistry and Molecular Medicine, University of California Davis, Davis, California, United States of America

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• Sajid Malik,

  Affiliation Human Genetics Program, Department of Animal Sciences, Quaid-i-Azam University Islamabad, 45320 Islamabad, Pakistan

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• Kehkashan Mazhar

  * E-mail: kehkashan_mbhatti@yahoo.com

  Affiliation Institute of Biomedical and Genetic Engineering, Islamabad, Pakistan

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