Progressive proptosis in a neonate.

Por O'Driscoll, D. A., O'Neill, M.
Publicado em 1998

A genetic etiology for DiGeorge syndrome: consistent deletions and microdeletions of 22q11.

Por Driscoll, D A, Budarf, M L, Emanuel, B S
Publicado em 1992

"CATCH 22" sans cardiac anomaly, thymic hypoplasia, cleft palate, and hypocalcaemia: cAtch 22. A common result of 22q11 deficiency?

Por Lipson, A, Emanuel, B, Colley, P, Fagan, K, Driscoll, D A
Publicado em 1994

Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotype.

Por Gottlieb, S, Driscoll, D A, Punnett, H H, Sellinger, B, Emanuel, B S, Budarf, M L
Publicado em 1998

The DiGeorge syndrome minimal critical region contains a goosecoid-like (GSCL) homeobox gene that is expressed early in human development.

Por Gottlieb, S, Emanuel, B S, Driscoll, D A, Sellinger, B, Wang, Z, Roe, B, Budarf, M L
Publicado em 1997

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis.

Por Driscoll, D A, Salvin, J, Sellinger, B, Budarf, M L, McDonald-McGinn, D M, Zackai, E H, Emanuel, B S
Publicado em 1993

Cerebellar atrophy in a patient with velocardiofacial syndrome.

Por Lynch, D R, McDonald-McGinn, D M, Zackai, E H, Emanuel, B S, Driscoll, D A, Whitaker, L A, Fischbeck, K H
Publicado em 1995

More Clinical Overlap between 22q11.2 Deletion Syndrome and CHARGE Syndrome than Often Anticipated

Por Corsten-Janssen, N., Saitta, S.C., Hoefsloot, L.H., McDonald-McGinn, D.M., Driscoll, D.A., Derks, R., Dickinson, K.A., Kerstjens-Frederikse, W.S., Emanuel, B.S., Zackai, E.H., van Ravenswaaij-Arts, C.M.A.
Publicado em 2013