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Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 26, 2009
FG syndrome, an X-linked multiple congenital anomaly syndrome: the clinical phenotype and an algorithm for diagnostic testingRobin Dawn Clark, John M Graham, Michael J Friez, et al.
American Journal of Medical Genetics. Part A|November 1, 2008
Behavior of 10 patients with FG syndrome (Opitz-Kaveggia syndrome) and the p.R961W mutation in the MED12 geneJohn M Graham, Jeannie Visootsak, Elisabeth Dykens, et al.
Nature Genetics|March 6, 2007
A recurrent mutation in MED12 leading to R961W causes Opitz-Kaveggia syndromeHiba Risheg, John M Graham, Robin D Clark, et al.
Molecular Metabolism|July 10, 2019
Phosphatidylserine decarboxylase is critical for the maintenance of skeletal muscle mitochondrial integrity and muscle massAhrathy Selathurai, Greg M Kowalski, Shaun A Mason, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|July 26, 2015
Randomized controlled trial of mycophenolate mofetil in children, adolescents, and adults with IgA nephropathyRonald J Hogg, R Curtis Bay, J Charles Jennette, et al.
Oncoimmunology|January 4, 2018
Interleukin-21 combined with PD-1 or CTLA-4 blockade enhances antitumor immunity in mouse tumor modelsKatherine E Lewis, Mark J Selby, Gregg Masters, et al.
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