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 journalArticle

Original languageEnglish
Pages (from-to)247-249
Number of pages3
JournalAmerican Journal of Human Genetics
Volume65
Issue number1
DOIs
Publication statusPublished - 1999

ASJC Scopus subject areas

  • Genetics

Cite this

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

In: American Journal of Human Genetics, Vol. 65, No. 1, 1999, p. 247-249.

Research output: Contribution to journalArticle

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 1999, 'Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/velocardiofacial syndrome without deletions within chromosome 22q11 [1]', American Journal of Human Genetics, vol. 65, no. 1, pp. 247-249. https://doi.org/10.1086/302468
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. / Mutations of UFD1L are not responsible for the majority of cases of DiGeorge syndrome/velocardiofacial syndrome without deletions within chromosome 22q11 [1]. In: American Journal of Human Genetics. 1999 ; Vol. 65, No. 1. pp. 247-249.
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AU - Osinga, J.

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