| Literature DB >> 1391972 |
M Asai1, Y Ito, T Iguchi, J Ito, N Okada, H Oishi.
Abstract
A boy with growth and mental retardation, flat occiput, high and broad forehead, blepharoptosis, narrow palpebral fissures, low set, malformed ears, short neck, anal atresia, deep sacral dimple is reported. High-resolution banding analysis showed terminal deletion of the short arm of chromosome 3 (46,XY,del(3)(p25.3)). Deletions of the short arm of chromosome 3 are relatively rare. The clinical features of the patient are compared with those of 19 previously reported cases.Entities:
Mesh:
Year: 1992 PMID: 1391972 DOI: 10.1007/BF01899740
Source DB: PubMed Journal: Jpn J Hum Genet ISSN: 0916-8478