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American Journal of Medical Genetics|July 1, 1991
Interstitial deletion of 4(q21q25) in a liveborn maleN C Rose, A Schneider, D M 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.Human Genetics|November 1, 1993
Human malformations similar to those in the mouse mutation disorganization (Ds)N H Robin, O O Adewale, D McDonald-McGinn, et al.Neuropsychologia|October 9, 2007
Overlapping numerical cognition impairments in children with chromosome 22q11.2 deletion or Turner syndromesT J Simon, Y Takarae, T DeBoer, et al.American Journal of Medical Genetics. Part A|April 1, 2004
Autosomal dominant inheritance of infantile myofibromatosisDina J Zand, Dale Huff, David Everman, et al.American Journal of Medical Genetics. Part A|October 12, 2013
Congenital heart defects in oculodentodigital dysplasia: Report of two casesKosuke Izumi, Andrew M Lippa, Alisha Wilkens, et al.Pediatric Radiology|August 6, 2016
Characteristic calcaneal ossification: an additional early radiographic finding in infants with fibrodysplasia ossificans progressivaSachi Hasegawa, Teresa Victoria, Hülya Kayserili, et al.The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|January 20, 2018
Crouzon with Acanthosis Nigricans and Odontogenic Tumors: A Rare Form of Syndromic CraniosynostosisWen Xu, Donna M McDonald-McGinn, Alexandra J Melchiorre, et al.Nature Genetics|October 1, 1996
Identical mutations in three different fibroblast growth factor receptor genes in autosomal dominant craniosynostosis syndromesG A Bellus, K Gaudenz, E H Zackai, et al.American Journal of Medical Genetics|February 6, 1999
TWIST gene mutation in a patient with radial aplasia and craniosynostosis: further evidence for heterogeneity of Baller-Gerold syndromeK W Gripp, C A Stolle, L Celle, et al.Pageof 63