1. Velocardiofacial (Shprintzen) syndrome: an important syndrome for the dysmorphologist to recognise;Lipson, A.H.; Yuille, D.; Angel, M.; Thompson, P.G.; Vandervoord, J.G.; Beckenham, E.J.;Jf Med Genet,1991
2. DiGeorge syndrome: part of CATCH 22;Wilson, D.I.; Bum, J.; Scambler, P.; Goodship, J.;Jf Med Genet,1993
3. Clinical and molecular study of DiGeorge sequence;Levy-Mozziconacci, A.; Wemert, F.; Scambler, P.;EurJ Pediatr,1994
4. A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q1 1. Am J7 Hum Genet;Driscoll, D.A.; Budarf, M.L.; Emanuel, B.S.,1992
5. Decrease in thyrocalcitonin-containing cells and analysis of other congenital anomalies in 11 patients with DiGeorge anomaly;Palacios, J.; Gamallo, C.; Garcia, M.; Rodriguez, J.I.;AmJMed Genet,1993