Detection of 1(p36) deletion in patients with developmental delay and facial dysmorphism
Dalia Farouk Ahmed Hussein;
Abstract
1p36 deletion syndrome is considered to be one of the commonest chromosome deletion syndromes. It results in a clinically recognizable phenotype including dysmorphic features, mental retardation, developmental delay and others e.g. hearing abnormalities,
Other data
| Title | Detection of 1(p36) deletion in patients with developmental delay and facial dysmorphism | Other Titles | الكشف عن نقص جزء من كروموسوم ( 1(p36 في مرضى بطء النمو ومظاهر تشوهات الوجه | Authors | Dalia Farouk Ahmed Hussein | Keywords | Detection of 1(p36) deletion in patients with developmental delay and facial dysmorphism | Issue Date | 2010 | Description | 1p36 deletion syndrome is considered to be one of the commonest chromosome deletion syndromes. It results in a clinically recognizable phenotype including dysmorphic features, mental retardation, developmental delay and others e.g. hearing abnormalities, |
Attached Files
| File | Size | Format | |
|---|---|---|---|
| 101045r3719.pdf | 415.39 kB | Adobe PDF | View/Open |
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