header
Local cover image
Local cover image
Image from OpenLibrary

Relation between brain morphology and language profile in fragile X syndrome / Rasha Samy Abdelaziz ; Supervised Hossam Mohamed Eldessouky , Nagwa Abdelmeguid Mohamed , Elham Ahmed Shaheen

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Rasha Samy Abdelaziz , 2010Description: 172 P. : charts , facsimiles ; 25cmOther title:
  • العلاقة بين التكوين الشكلى للمخ والصورة اللغوية فى متلازمة هشاشة كروموزوم اكس [Added title page title]
Subject(s): Online resources: Available additional physical forms:
  • Issued also as CD
Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of E.N.T Summary: Fragile X syndrome ( FXS ) is one of the most prevalent forms of heritable mental retardation and developmental delay in males it is caused by a defective gene on the X chromosome the syndrome is caused by the silencing of a single gene ( fragile X mental retardation-1; FMR1 ) and the lack of expression of its protein product ( fragile X mental retardation-1 protein; FMRP )
Tags from this library: No tags from this library for this title. Log in to add tags.
Star ratings
    Average rating: 0.0 (0 votes)
Holdings
Item type Current library Home library Call number Copy number Status Barcode
Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.12.M.Sc.2010.Ra.R (Browse shelf(Opens below)) Not for loan 01010110053669000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.12.M.Sc.2010.Ra.R (Browse shelf(Opens below)) 53669.CD Not for loan 01020110053669000

Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of E.N.T

Fragile X syndrome ( FXS ) is one of the most prevalent forms of heritable mental retardation and developmental delay in males it is caused by a defective gene on the X chromosome the syndrome is caused by the silencing of a single gene ( fragile X mental retardation-1; FMR1 ) and the lack of expression of its protein product ( fragile X mental retardation-1 protein; FMRP )

Issued also as CD

There are no comments on this title.

to post a comment.

Click on an image to view it in the image viewer

Local cover image