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Fragile X mental retardation 1 gene and metabolic biomarkers in autism and fragile X syndrome / Rehab Mohamed Osama Khalil ; Supervised Hazem Mahmoud Atta , Nagwa Abdelmeguid , Laila Ahmed Rashed

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Rehab Mohamed Osama Khalil , 2012Description: 205P. : charts , facsimiles ; 25cmOther title:
  • دراسة جين التأخر العقلى ودلالات كيميائية فى مرض التوحد وهشاشة كروموسوم اكس [Added title page title]
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  • Issued also as CD
Dissertation note: Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Medical Biochemistry Summary: Fragile X is the most common single gene cause of autusm , responsible for 2 % to 6 % of all cases of autism , Approximately 30% of males with FXS have full autism . Genes known to be causes of ASD intteract with the translational pathway defective in FXS and it has been hypothesized that there will be substantial overlap in molecular pathways and mechanisms of synaptic dysfunction between FXS and ASD
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Item type Current library Home library Call number Copy number Status Date due Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.03.Ph.D.2012.Re.F (Browse shelf(Opens below)) Not for loan 01010110057890000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.03.Ph.D.2012.Re.F (Browse shelf(Opens below)) 57890.CD Not for loan 01020110057890000

Thesis (Ph.D.) - Cairo University - Faculty of Medicine - Department of Medical Biochemistry

Fragile X is the most common single gene cause of autusm , responsible for 2 % to 6 % of all cases of autism , Approximately 30% of males with FXS have full autism . Genes known to be causes of ASD intteract with the translational pathway defective in FXS and it has been hypothesized that there will be substantial overlap in molecular pathways and mechanisms of synaptic dysfunction between FXS and ASD

Issued also as CD

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