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Teaching and Learning in Medicine|July 11, 2014
Diversity efforts, admissions, and national rankings: can we align priorities?Caren A Heller, Sandra Hurtado Rúa, Madhu Mazumdar, et al.
Hormone Research in Paediatrics|June 28, 2014
Whole exome sequencing to identify genetic causes of short statureMichael H Guo, Yiping Shen, Emily C Walvoord, et al.
The Journal of Clinical Endocrinology and Metabolism|June 18, 2013
Large-scale pooled next-generation sequencing of 1077 genes to identify genetic causes of short statureSophie R Wang, Heather Carmichael, Shayne F Andrew, et al.
Journal of Cardiovascular Pharmacology and Therapeutics|April 17, 2014
Lipids, safety parameters, and drug concentrations after an additional 2 years of treatment with anacetrapib in the DEFINE studyAntonio M Gotto, Uma Kher, Manash Shankar Chatterjee, et al.
European Journal of Medical Genetics|July 9, 2013
An interstitial, apparently-balanced chromosomal insertion in the etiology of Langer-Giedion syndrome in an Asian familyByung-Joo Min, Jung Min Ko, Myung-Eui Seo, et al.
Human Mutation|February 24, 2015
Heterozygous mutations in natriuretic peptide receptor-B (NPR2) gene as a cause of short statureSophie R Wang, Christina M Jacobsen, Heather Carmichael, et al.
The Journal of Clinical Endocrinology and Metabolism|August 31, 2012
Novel microcephalic primordial dwarfism disorder associated with variants in the centrosomal protein nineinAndrew Dauber, Stephen H Lafranchi, Zoltan Maliga, et al.
Journal of Pediatric Gastroenterology and Nutrition|January 28, 2015
Functional significance of single nucleotide polymorphisms in the lactase gene in diverse US patients and evidence for a novel lactase persistence allele at -13909 in those of European ancestryNana Yaa Baffour-Awuah, Sarah Fleet, Robert K Montgomery, et al.
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