Journal
CYTOGENETICS AND CELL GENETICS
Volume 91, Issue 1-4, Pages 138-140Publisher
KARGER
DOI: 10.1159/000056834
Keywords
-
Categories
Ask authors/readers for more resources
Non-syndromic trigonocephaly is a heterogeneous entity; in most cases the origin is unknown. Rare cases with autosomal dominant and recessive inheritance exist. Here the mutational screening often patients in the FGFR1, 2, and 3 genes and the TWIST gene causative of autosomal dominant craniosynostosis syndromes was reported. In one girl an unusual FGFR1 mutation was found. Copyright (C) 2001 S. Karger AG, Basel.
Authors
I am an author on this paper
Click your name to claim this paper and add it to your profile.
Reviews
Recommended
No Data Available