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The Journal of Thoracic and Cardiovascular Surgery|April 13, 2010
Genetic factors are important determinants of impaired growth after infant cardiac surgeryNancy Burnham, Richard F Ittenbach, Virginia A Stallings, et al.
The Journal of Biological Chemistry|September 6, 1996
Identification of a mutation in a GATA binding site of the platelet glycoprotein Ibbeta promoter resulting in the Bernard-Soulier syndromeL B Ludlow, B P Schick, M L Budarf, et al.
Clinical Immunology and Immunopathology|March 7, 1998
Lack of correlation between impaired T cell production, immunodeficiency, and other phenotypic features in chromosome 22q11.2 deletion syndromesK E Sullivan, A F Jawad, P Randall, et al.
American Journal of Medical Genetics. Part A|July 22, 2004
Increased prevalence of unprovoked seizures in patients with a 22q11.2 deletionAmy Kao, Juliana Mariani, Donna M McDonald-McGinn, et al.
Nature|December 12, 1996
Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndromeE Trivier, D De Cesare, S Jacquot, et al.
Journal of Pediatric Psychology|March 10, 2006
Increased prevalence of ADHD in Turner syndrome with no evidence of imprinting effectsHeather F Russell, Deeann Wallis, Michèle M M Mazzocco, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|May 9, 2014
Perioperative risk factors in patients with 22q11.2 deletion syndrome requiring surgery for velopharyngeal dysfunctionCarrie Stransky, Marten Basta, Donna M McDonald-McGinn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 8, 2001
Phenotype of the 22q11.2 deletion in individuals identified through an affected relative: cast a wide FISHing net!D M McDonald-McGinn, M K Tonnesen, A Laufer-Cahana, et al.
Clinical Genetics|September 25, 2008
Identification of a previously unrecognized microdeletion syndrome of 16q11.2q12.2B C Ballif, A Theisen, D M McDonald-McGinn, et al.
American Journal of Medical Genetics. Part A|February 13, 2013
Novel FREM1 mutations expand the phenotypic spectrum associated with Manitoba-oculo-tricho-anal (MOTA) syndrome and bifid nose renal agenesis anorectal malformations (BNAR) syndromeJared Nathanson, Daniel T Swarr, Amihood Singer, et al.
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