Deletions encompassing 1q41q42.1 and clinical features of autosomal dominant Robinow syndrome

Author(s):
Mazzeu, J.F.; Vianna-Morgante, A.M.; Krepischi, A.C.V.; Oudakker, A.; Rosenberg, C.; Szuhai, K. (0000-0002-1228-4245); McGill, J.; MacCraughan, J.; Bokhoven, H. van; Brunner, H.G.
Published
2010
Publication type
Article / Letter to editor
congenital diaphragmatic-hernia microdeletion syndrome corpus-callosum critical region gene translocation mutation family locus ror2
Date issued
2010-04-30
Language
English
Is part of
Clinical Genetics (2010), Vol. 77, no. 4, p. 404-407
hdl
1887/109661