| Literature DB >> 2469548 |
B Roland1, R B Lowry, A S Robertson, D M Cox.
Abstract
A case of an interstitial deletion of chromosome 13, identified as 46,XY,del(13)(q22q31), is reported in a child with psychomotor retardation, prominent low-set ears, epicanthus, hypertelorism, broad nasal bridge, hypoplastic fifth fingers and abnormal dermatoglyphics. This patient is compared to others in the literature with a similar deletion.Entities:
Mesh：
Year: 1989 PMID： 2469548 DOI： 10.1111/j.1399-0004.1989.tb02943.x
Source DB: PubMed Journal: Clin Genet ISSN： 0009-9163 Impact factor: 4.438