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Journal of AAPOS : the Official Publication of the American Association for Pediatric Ophthalmology and Strabismus|October 31, 2006
Ocular phenotype correlations in patients with TWIST versus FGFR3 genetic mutationsSuzanne K Jadico, Alexandra Huebner, Donna M McDonald-McGinn, et al.
American Journal of Medical Genetics|May 16, 1997
Further clinical delineation and increased morbidity in males with osteopathia striata with cranial sclerosis: an X-linked disorder?J E Pellegrino, D M McDonald-McGinn, A Schneider, et al.
American Journal of Medical Genetics. Part A|August 6, 2013
Expanding the spectrum of microdeletion 4q21 syndrome: a partial phenotype with incomplete deletion of the minimal critical region and a new association with cleft palate and Pierre Robin sequenceElizabeth Bhoj, Sara Halbach, Donna McDonald-McGinn, et al.
The Journal of Craniofacial Surgery|May 21, 2020
The Role of Precedex in Post-Operative Pain Management Following Craniosynostosis RepairHope Xu, Anthony Bui, Stav Brown, et al.
The Journal of Pediatrics|August 1, 1982
The association of the DiGeorge anomalad with partial monosomy of chromosome 22R I Kelley, E H Zackai, B S Emanuel, et al.
Archives of Otolaryngology--Head & Neck Surgery|November 17, 2004
Tracheal anomalies in Pfeiffer syndromeNeil G Hockstein, Donna McDonald-McGinn, Elaine Zackai, et al.
American Journal of Medical Genetics|February 2, 1996
Developmental profile in a patient with monosomy 10q and dup(17p) associated with a peripheral neuropathyJ E Pellegrino, L Pellegrino, N B Spinner, et al.
Blood|October 4, 2003
T-cell homeostasis in humans with thymic hypoplasia due to chromosome 22q11.2 deletion syndromeLisa M Piliero, Amy N Sanford, Donna M McDonald-McGinn, 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|May 1, 1991
Congenital nystagmus in a (46,XX/45,X) mosaic woman from a family with X-linked congenital nystagmusD H Gutmann, M L Brooks, B S Emanuel, et al.
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