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American Journal of Medical Genetics. Part A|February 27, 2010
Novel ANKH mutation in a patient with sporadic craniometaphyseal dysplasiaAllison Zajac, Seung-Hak Baek, Imad Salhab, et al.
Diabetes|July 13, 2010
Large copy-number variations are enriched in cases with moderate to extreme obesityKai Wang, Wei-Dong Li, Joseph T Glessner, et al.
Cerebral Cortex (New York, N.Y. : 1991)|January 15, 2014
Imaging patterns of brain development and their relationship to cognitionGuray Erus, Harsha Battapady, Theodore D Satterthwaite, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|February 8, 2022
Genetic Analysis in African American Children Supports Ancestry-Specific Neuroblastoma SusceptibilityAlessandro Testori, Zalman Vaksman, Sharon J Diskin, et al.
Diabetes|April 23, 2008
Association analysis of type 2 diabetes Loci in type 1 diabetesHui-Qi Qu, Struan F A Grant, Jonathan P Bradfield, et al.
Molecular Oncology|August 14, 2024
Copy number variations contribute to malignant tumor development in children with serious birth defectsYichuan Liu, Joseph Glessner, Hui-Qi Qu, et al.
American Journal of Medical Genetics. Part A|October 17, 2015
Aortic coarctation and carotid artery aneurysm in a patient with Hardikar syndrome: Cardiovascular implications for affected individualsKaitlin M Ryan, Alexander R Ellis, Reem Raafat, et al.
Metabolomics : Official Journal of the Metabolomic Society|December 2, 2022
Metabolomic profiling for dyslipidemia in pediatric patients with sickle cell disease, on behalf of the IHCC consortiumHui-Qi Qu, Joseph Glessner, Jingchun Qu, et al.
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