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Journal of Affective Disorders|March 10, 2009
Affective disorders and other psychiatric diagnoses in children and adolescents with 22q11.2 Deletion SyndromeEdith M Jolin, Ronald A Weller, Naushad R Jessani, et al.
American Journal of Medical Genetics. Part A|October 18, 2011
Ablepharon-Macrostomia syndrome--extension of the phenotypeStaci Kallish, Donna M McDonald-McGinn, Mieke M van Haelst, et al.
American Journal of Medical Genetics|March 13, 1995
Mosaicism for a chromosome 8-derived minute marker chromosome in a patient with manifestations of trisomy 8 mosaicismN B Spinner, K R Grace, N L Owens, et al.
American Journal of Medical Genetics. Part A|January 14, 2021
Hyperinsulinism in an individual with an EP300 variant of Rubinstein-Taybi syndromeK Taylor Wild, Tomoki T Nomakuchi, Sarah E Sheppard, et al.
Clinical Immunology (Orlando, Fla.)|December 23, 2015
B cell development in chromosome 22q11.2 deletion syndromeBeata Derfalvi, Kelly Maurer, Donna M McDonald McGinn, et al.
The Journal of Bone and Joint Surgery. American Volume|February 1, 1987
Metatropic dwarfism. Uncoupling of endochondral and perichondral growthS D Boden, F S Kaplan, M D Fallon, et al.
The Journal of Pediatrics|August 10, 2000
Dysphagia in children with a 22q11.2 deletion: unusual pattern found on modified barium swallowP S Eicher, D M McDonald-Mcginn, C A Fox, et al.
American Journal of Medical Genetics|November 15, 1994
Non-immune hydrops fetalis associated with impaired fetal movement: a case report and reviewN H Robin, M T Curtis, W Mulla, et al.
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