Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/ velocardiofacial syndrome without deletions within chromosome 22q11

Wadey, R McKie, J Papapetrou, C Sutherland, H Lohman, F Osinga, J Frohn, I Hofstra, R Meijers, C Amati, F Conti, E Pizzuti, A Dallapiccola, B Novelli, G Scambler, P

R. Wadey et al., Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/ velocardiofacial syndrome without deletions within chromosome 22q11, AM J HU GEN, 65(1), 1999, pp. 247-249

24

Research/Laboratory Medicine & Medical Tecnology","Molecular Biology & Genetics

AMERICAN JOURNAL OF HUMAN GENETICS

00029297 → ACNP

65

1

1999

247 - 249

ISI

0002-9297(199907)65:1<247:MOUANR>2.0.ZU;2-F