Abstract
Del(3)(p25pter) is associated with a characteristic multiple congenital anomalies/mental retardation syndrome. Early recognition of these manifestations and identification of the chromosome defect are essential for proper management and counseling.
Original language | English (US) |
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Pages (from-to) | 108-112 |
Number of pages | 5 |
Journal | American Journal of Medical Genetics |
Volume | 33 |
Issue number | 1 |
DOIs | |
State | Published - 1989 |
All Science Journal Classification (ASJC) codes
- Genetics(clinical)