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Neurology|November 18, 1998
Polymicrogyria in chromosome 22 delection syndromeP M Bingham, D Lynch, D McDonald-McGinn, et al.Pediatrics|December 4, 2001
Cardiovascular anomalies in patients diagnosed with a chromosome 22q11 deletion beyond 6 months of ageD B McElhinney, D McDonald-McGinn, E H Zackai, et al.Advances in Pediatrics|August 2, 2001
The 22q11.2 deletion syndromeB S Emanuel, D McDonald-McGinn, S C Saitta, et al.American Journal of Medical Genetics|November 1, 1993
New finding of Schinzel-Giedion syndrome: a case with a malignant sacrococcygeal teratomaN H Robin, K Grace, T G DeSouza, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2001
Neuropsychological profile of children and adolescents with the 22q11.2 microdeletionM Woodin, P P Wang, D Aleman, et al.Clinical Genetics|December 1, 1993
De novo interstitial deletion of the long arm of chromosome 3: 46,XX,del(3)(q25.1q26.1)N H Robin, M Magnusson, D McDonald-McGinn, et al.Clinical Immunology (Orlando, Fla.)|May 18, 2010
Secondary immunologic consequences in chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome)R Zemble, E Luning Prak, K McDonald, et al.Journal of Medical Genetics|July 1, 1994
Paternal transmission of congenital myotonic dystrophyJ Bergoffen, J Kant, J Sladky, et al.American Journal of Medical Genetics|October 28, 1997
Enlarged Sylvian fissures in infants with interstitial deletion of chromosome 22q11P M Bingham, R A Zimmerman, D McDonald-McGinn, et al.American Journal of Medical Genetics|March 13, 1995
Classical Noonan syndrome is not associated with deletions of 22q11N H Robin, B Sellinger, D McDonald-McGinn, et al.Pageof 3