Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/velocardiofacial syndrome without deletions within chromosome 22q11 [1]

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

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)247-249
Number of pages3
JournalAmerican Journal of Human Genetics
Issue number1
Publication statusPublished - 1999

ASJC Scopus subject areas

  • Genetics

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