INTERSTITIAL DELETION OF 17P11.2 - CASE-REPORT AND REVIEW
- 1 January 1988
- journal article
- review article
- Vol. 31 (1) , 36-38
Abstract
A child with mental retardation and multiple congenital abnormalities, including brachycephaly, an unusual facies, brachydactyly, clinodactyly and bilateral talipes valgus, was found to have a small interstitial deletion of the short arm of chromosome 17. The clinical features and cytogenetic observations are compared with those in previously reported cases.This publication has 2 references indexed in Scilit:
- Interstitial deletion of (17)(p11.2p11.2): Report of six additional patients with a new chromosome deletion syndromeAmerican Journal of Medical Genetics, 1986
- Interstitial deletion of (17)(p11.2p11.2) in nine patientsAmerican Journal of Medical Genetics, 1986