Interstitial deletion of 17p11.2: case report and review.

Hamill Ma, Roberts Sh, Maguire Mj, Laurence Km

PubMed · 1988 · 14 citations · 0 references

Concepts

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.