D M McDonald-McGinn

Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion.

E. Zackai, B. Emanuel, D. McDonald-McGinn, 1996, American journal of medical genetics.

Bilateral microtia and cleft palate in cousins with Diamond-Blackfan anemia.

E. Zackai, K. Gripp, D. McDonald-McGinn, 2001, American journal of medical genetics.

Psychoeducational profile of the 22q11.2 microdeletion: A complex pattern.

E. Zackai, B. Emanuel, D. Driscoll, 1999, The Journal of pediatrics.

Deletions and microdeletions of 22q11.2 in velo-cardio-facial syndrome.

E. Zackai, N. Spinner, R. Shprintzen, 1992, American journal of medical genetics.

Cognitive and behavior profile of preschool children with chromosome 22q11.2 deletion.

E. Zackai, B. Clark, A. Jawad, 1999, American journal of medical genetics.

The Philadelphia story: the 22q11.2 deletion: report on 250 patients.

E. Zackai, K. Sullivan, B. Emanuel, 1999, Genetic counseling.

Juvenile rheumatoid arthritis-like polyarthritis in chromosome 22q11.2 deletion syndrome (DiGeorge anomalad/velocardiofacial syndrome/conotruncal anomaly face syndrome).

E. Zackai, K. Sullivan, B. Emanuel, 1997, Arthritis and rheumatism.

Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion.

E. Zackai, B. Clark, K. Sullivan, 1995, American journal of medical genetics.