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Clinical Chemistry|February 6, 2016
Systematic Evaluation of Sanger Validation of Next-Generation Sequencing VariantsTyler F Beck, James C Mullikin, , et al.JCO Clinical Cancer Informatics|January 18, 2019
Assessing the Training and Research Environment for Genomics, Bioinformatics, and Immunology in Radiation OncologyKent W Mouw, Tyler F Beck, Judith C Keen, et al.American Journal of Medical Genetics. Part A|July 17, 2009
A 1q42 deletion involving DISC1, DISC2, and TSNAX in an autism spectrum disorderJaime M Williams, Tyler F Beck, David M Pearson, et al.Plos One|March 29, 2013
Novel frem1-related mouse phenotypes and evidence of genetic interactions with gata4 and slit3Tyler F Beck, Oleg A Shchelochkov, Zhiyin Yu, et al.Plos One|January 24, 2014
Identification of critical regions and candidate genes for cardiovascular malformations and cardiomyopathy associated with deletions of chromosome 1p36Hitisha P Zaveri, Tyler F Beck, Andrés Hernández-García, et al.Human Molecular Genetics|June 23, 2012
Mouse model reveals the role of SOX7 in the development of congenital diaphragmatic hernia associated with recurrent deletions of 8p23.1Margaret J Wat, Tyler F Beck, Andrés Hernández-García, et al.International Journal of Radiation Oncology, Biology, Physics|January 17, 2019
Analysis of the 2017 American Society for Radiation Oncology (ASTRO) Research PortfolioJames B Yu, Tyler F Beck, Mitchell S Anscher, et al.American Journal of Medical Genetics. Part A|March 5, 2015
FBN1 contributing to familial congenital diaphragmatic herniaTyler F Beck, Philippe M Campeau, Shalini N Jhangiani, et al.Human Molecular Genetics|December 11, 2012
Deficiency of FRAS1-related extracellular matrix 1 (FREM1) causes congenital diaphragmatic hernia in humans and miceTyler F Beck, Danielle Veenma, Oleg A Shchelochkov, et al.Human Molecular Genetics|April 5, 2018
The role of FREM2 and FRAS1 in the development of congenital diaphragmatic herniaValerie K Jordan, Tyler F Beck, Andres Hernandez-Garcia, et al.Pageof 1