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Journal of Behavior Therapy and Experimental Psychiatry|May 11, 2012
Covariation bias for food-related control is associated with eating disorders symptoms in normal adolescentsBirgit Mayer, Peter Muris, Nancy Kramer Freher, et al.
Child Psychiatry and Human Development|May 5, 2010
Children's internal attributions of anxiety-related physical symptoms: age-related patterns and the role of cognitive development and anxiety sensitivityPeter Muris, Birgit Mayer, Nancy Kramer Freher, et al.
European Journal of Medical Genetics|February 28, 2012
De novo microdeletion of Xp11.3 exclusively encompassing the monoamine oxidase A and B genes in a male infant with episodic hypotonia: a genomics approach to personalized medicineRyan E O'Leary, Jean C Shih, Keith Hyland, et al.
European Journal of Medical Genetics|September 18, 2014
19q13.32 microdeletion syndrome: three new casesAngela Castillo, Nancy Kramer, Charles E Schwartz, et al.
American Journal of Medical Genetics. Part A|September 18, 2009
Genomic duplication of PTPN11 is an uncommon cause of Noonan syndromeJohn M Graham, Nancy Kramer, Bassem A Bejjani, et al.
American Journal of Medical Genetics. Part A|December 21, 2013
De novo exon 1 missense mutations of SKI and Shprintzen-Goldberg syndrome: two new cases and a clinical reviewP Y Billie Au, Hilary E Racher, John M Graham, et al.
Biomedical Instrumentation & Technology|April 23, 2013
A roundtable discussion: home healthcare-not a hospital in the homeMary K Logan, Chuck Parker, Daryle Gardner-Bonneau, et al.
American Journal of Medical Genetics. Part A|January 10, 2012
Megalencephaly-capillary malformation (MCAP) and megalencephaly-polydactyly-polymicrogyria-hydrocephalus (MPPH) syndromes: two closely related disorders of brain overgrowth and abnormal brain and body morphogenesisGhayda M Mirzaa, Robert L Conway, Karen W Gripp, et al.
American Journal of Medical Genetics. Part A|April 30, 2015
Clinical management of patients with ASXL1 mutations and Bohring-Opitz syndrome, emphasizing the need for Wilms tumor surveillanceBianca Russell, Jennifer J Johnston, Leslie G Biesecker, et al.
American Journal of Human Genetics|June 4, 2016
Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart DefectsLia Boyle, Mirjam M C Wamelink, Gajja S Salomons, et al.
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