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Human Mutation|April 3, 2007
Epistatic interactions with a common hypomorphic RET allele in syndromic Hirschsprung diseaseL de Pontual, A Pelet, M Clement-Ziza, et al.Genetic Epidemiology|August 19, 2010
Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndromeAdam E Locke, Kenneth J Dooley, Stuart W Tinker, et al.Journal of Medical Genetics|February 24, 2011
Case series: 2q33.1 microdeletion syndrome--further delineation of the phenotypeM Balasubramanian, K Smith, L Basel-Vanagaite, et al.Journal of Human Genetics|January 20, 2017
Variants on chromosome 4q21 near PKD2 and SIBLINGs are associated with dental cariesScott Eckert, Eleanor Feingold, Margaret Cooper, et al.G3 (Bethesda, Md.)|July 22, 2015
Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal DefectsDhanya Ramachandran, Zhen Zeng, Adam E Locke, et al.The Lancet. Oncology|May 14, 2021
Loncastuximab tesirine in relapsed or refractory diffuse large B-cell lymphoma (LOTIS-2): a multicentre, open-label, single-arm, phase 2 trialPaolo F Caimi, Weiyun Ai, Juan Pablo Alderuccio, et al.Bioorganic & Medicinal Chemistry|March 30, 2007
Further modification on phenyl acetic acid based quinolines as liver X receptor modulatorsBaihua Hu, James Jetter, David Kaufman, et al.Plos Genetics|August 2, 2018
Investigating the shared genetics of non-syndromic cleft lip/palate and facial morphologyLaurence J Howe, Myoung Keun Lee, Gemma C Sharp, et al.Journal of Dental Research|May 10, 2014
Genetic Association of MPPED2 and ACTN2 with Dental CariesB O C Stanley, E Feingold, M Cooper, et al.Frontiers in Genetics|November 9, 2018
SNPs Associated With Testosterone Levels Influence Human Facial MorphologyJasmien Roosenboom, Karlijne Indencleef, Myoung Keun Lee, et al.Pageof 186