Dystrophin gene analysis as a method of screening of carrier females in Egyptian families with DMD\BMD patients with comparison study of the deletion patterns as a primary step for prenatal diagnosis
Rasha El Sherif;
Abstract
DMD and BMD are common lethal neuromuscular genetic diseases. Only the disorder arises as a new mutation in one third of these patients. Mothers of affected males are DMD/BMD carriers in two thirds of the cases.
Since gene deletions account for approxim
Since gene deletions account for approxim
Other data
| Title | Dystrophin gene analysis as a method of screening of carrier females in Egyptian families with DMD\BMD patients with comparison study of the deletion patterns as a primary step for prenatal diagnosis | Other Titles | التحليل الوراثى لجين الديسروفين كوسيلة لعمل مسح شامل لعائللات مرضى ضمور العضلات حتى يتم الكشف المبكر للاناث حاملات المرض استعدادا لاجراء أبحاث ما قبل الحمل | Authors | Rasha El Sherif | Keywords | Dystrophin gene analysis as a method of screening of carrier females in Egyptian families with DMD\BMD patients with comparison study of the deletion patterns as a primary step for prenatal diagnosis | Issue Date | 2009 | Description | DMD and BMD are common lethal neuromuscular genetic diseases. Only the disorder arises as a new mutation in one third of these patients. Mothers of affected males are DMD/BMD carriers in two thirds of the cases. Since gene deletions account for approxim |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 83115rasha thesis UNIVERSITY.pdf | 622.74 kB | Adobe PDF | View/Open |
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