Review
doi: 10.1002/ajmg.1320330115.
Two infants with del(3)(p25pter) and a review of previously reported cases
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- PMID: 2665488
- DOI: 10.1002/ajmg.1320330115
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Review
Two infants with del(3)(p25pter) and a review of previously reported cases
Am J Med Genet.
1989 May.
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.
Comment in
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Terminal deletion of chromosome 3p in adults: a fourth observation.Am J Med Genet. 1990 Aug;36(4):519-20. doi: 10.1002/ajmg.1320360432. Am J Med Genet. 1990. PMID: 2389810 No abstract available.
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