Detection of mutations in PTPN11 gene in patients with noonan syndrome / Maha Mahmoud Ahmed Kobesiy ; Supervised Maged Mohammed A. Barakat , Mona Lotfi Essawi , Manal Fouad Ismail
Material type: TextLanguage: English Publication details: Cairo : Maha Mahmoud Ahmed Kobesiy , 2013Description: 132 P. : charts , facsimiles ; 25cmOther title:- لدى مرضى متلازمة نونان PTPN11 تحديد طفرات جين [Added title page title]
- Issued also as CD
Item type | Current library | Home library | Call number | Copy number | Status | Date due | Barcode | |
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Thesis | قاعة الرسائل الجامعية - الدور الاول | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.08.01.M.Sc.2013.Ma.D (Browse shelf(Opens below)) | Not for loan | 01010110061047000 | |||
CD - Rom | مخـــزن الرســائل الجـــامعية - البدروم | المكتبة المركزبة الجديدة - جامعة القاهرة | Cai01.08.01.M.Sc.2013.Ma.D (Browse shelf(Opens below)) | 61047.CD | Not for loan | 01020110061047000 |
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Thesis (M.Sc.) - Cairo University - Faculty of Pharmacy - Department of Biochemistry
Background : Noonan syndrome (NS) is inherited as an autosomal dominant disorder with dysmorphic facies, short stature and cardiac defects which can be caused by missense PTPN11 mutations . Protein tyrosine phosphatase non receptor 11 (PTPN11) encodes src homology 2 domain containing tyrosine phosphatase-2 (SHP-2), a protein tyrosine phosphatase that acts in signal transduction downstream to growth factors and cytokines
Issued also as CD
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