Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

Author:

Ryan A K,Goodship J A,Wilson D I,Philip N,Levy A,Seidel H,Schuffenhauer S,Oechsler H,Belohradsky B,Prieur M,Aurias A,Raymond F L,Clayton-Smith J,Hatchwell E,McKeown C,Beemer F A,Dallapiccola B,Novelli G,Hurst J A,Ignatius J,Green A J,Winter R M,Brueton L,Brondum-Nielsen K,Scambler P J

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference19 articles.

1. Velocardiofacial (Shprintzen) syndrome: an important syndrome for the dysmorphologist to recognise;Lipson, A.H.; Yuille, D.; Angel, M.;_7 Med Genet,1991

2. DiGeorge syndrome and related syndromes associated with 22ql 1.2 deletions. A review;Demczuk, S.; Aurias, A.;Ann Genet (Paris),1995

3. DiGeorge syndrome: part of CATCH 22;Wilson, D.I.; Burn, J.; Scambler, P.; Goodship, J.;7 Med Genet,1993

4. Cerebellar atrophy in a patient with velocardiofacial syndrome;Lynch, D.R.; McDonald-McGinn, D.M.; Zackai, E.H.,1995

5. Cayler cardiofacial syndrome and del 22ql 1: part of the CATCH22 phenotype;Giannotti, A.; Digilio, M.C.; Marino, B.; Mingarelli, R.; Dallapiccola, B.;Am _7 Med Genet,1994

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