Ring chromosome 15 in a patient with features of Fryns' syndrome.
Open Access
- 1 July 1989
- journal article
- case report
- Published by BMJ in Journal of Medical Genetics
- Vol. 26 (7) , 469-470
- https://doi.org/10.1136/jmg.26.7.469
Abstract
A stillborn male infant with a ring chromosome 15 and some features compatible with Fryns' syndrome is presented. Neither diagnosis is common and the overlap may be of significance.Keywords
This publication has 3 references indexed in Scilit:
- Monosomy and trisomy of 15q24→qter in a family with a translocation t(6;15)(P25;q24)Clinical Genetics, 2008
- Severe Growth Failure Associated with Atrophic Intestinal Mucosa and Ring Chromosome 15Acta Paediatrica, 1986
- Ring chromosome 15 syndromeHuman Genetics, 1979