The 9p- deletion syndrome A patient with a 45,XX,-9,-15, + t(9/15) constitution due to maternal 3:l meiotic disjunction
- 1 February 1977
- journal article
- research article
- Published by Wiley in Clinical Genetics
- Vol. 11 (2) , 219-223
- https://doi.org/10.1111/j.1399-0004.1977.tb01303.x
Abstract
Deletion of the short arm of chromosome 9, derived from a 3:1 meiotic segregation in the mother, carrier of a balanced 9/15 translocation, was found in a 3‐year‐old female. Severe psychomotor retardation with delayed speech, brachicephaly, flat occiput, hypertelorism and long upper lip were the main signs in the girl.This publication has 4 references indexed in Scilit:
- The Prader-Willi syndrome with a 15/15 translocation. Case report and review of the literature.Journal of Medical Genetics, 1976
- 9P- SYNDROME1976
- Mental retardation and congenital malformations associated with a ring chromosome 9Human Genetics, 1976
- C-Group Chromosome Abnormality (? 10p-)American Journal of Diseases of Children, 1970