Format

Send to

Choose Destination
Clin Genet. 1988 Oct;34(4):230-45.

Coffin-Lowry syndrome: a multicenter study.

Author information

1
Unité de Génétique, Université de Nancy, France.

Abstract

The Coffin-Lowry syndrome is an inherited syndrome of mental retardation, characteristic facies and skeletal anomalies. The occurrence of severe manifestations in males, with no instance of male-to-male transmission, suggests an X-linked inheritance. The paper describes seven families from five European Centers.

PMID:
3069251
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Wiley
Loading ...
Support Center