Developmental delay and dysmorphic features associated with a previously undescribed deletion on chromosome 1.
Open Access
- 1 August 1995
- journal article
- case report
- Published by BMJ in Journal of Medical Genetics
- Vol. 32 (8) , 636-637
- https://doi.org/10.1136/jmg.32.8.636
Abstract
We report an 18 month old girl with developmental delay, dysmorphic features, and a karyotype 46,XX,del (1) (p32.1p32.3). To our knowledge the clinical features associated with this deletion have not been reported previously.Keywords
This publication has 3 references indexed in Scilit:
- De novo interstitial deletion of 1p (pter----p34.1::p32.3----qter).Journal of Medical Genetics, 1991
- Two cases of interstitial deletion 1p.Journal of Medical Genetics, 1991
- Deletion of chromosome 1p: a short reviewClinical Genetics, 1990