A novel mutation (a886g) in exon 5 of FGFR2 in members of a...

Journal of Medical Genetics 1997 / 05 Vol. 34; Iss. 5

A novel mutation (a886g) in exon 5 of FGFR2 in members of a family with Crouzon phenotype and plagiocephaly.

Steinberger, D, Collmann, H, Schmalenberger, B, Muller, U
How much do you like this book?
What’s the quality of the file?
Download the book for quality assessment
What’s the quality of the downloaded files?
Volume:
34
Language:
english
Journal:
Journal of Medical Genetics
DOI:
10.1136/jmg.34.5.420
Date:
May, 1997
File:
PDF, 856 KB
english, 1997
Conversion to is in progress
Conversion to is failed