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American Journal of Medical Genetics. Part A|February 6, 2021
A novel heterotaxy gene: Expansion of the phenotype of TTC21B-spectrum diseaseAlanna Strong, Dong Li, Frank Mentch, et al.Human Heredity|June 9, 2012
Two-stage extreme phenotype sequencing design for discovering and testing common and rare genetic variants: efficiency and powerGuolian Kang, Dongyu Lin, Hakon Hakonarson, et al.Endocrine Reviews|December 17, 2009
Can the genetics of type 1 and type 2 diabetes shed light on the genetics of latent autoimmune diabetes in adults?Struan F A Grant, Hakon Hakonarson, Stanley SchwartzCurrent Diabetes Reports|October 12, 2015
Progress in understanding type 1 diabetes through its genetic overlap with other autoimmune diseasesJeffrey D Roizen, Jonathan P Bradfield, Hakon HakonarsonBest Practice & Research. Clinical Gastroenterology|November 11, 2015
The genetic basis of eosinophilic esophagitisPatrick M A Sleiman, Michael March, Hakon HakonarsonInternational Journal of General Medicine|May 3, 2013
Genetic polymorphisms and associated susceptibility to asthmaMichael E March, Patrick Ma Sleiman, Hakon HakonarsonJournal of the American Heart Association|November 16, 2022
Genetics of BAG3: A Paradigm for Developing Precision Therapies for Dilated CardiomyopathiesHui-Qi Qu, Arthur M Feldman, Hakon HakonarsonChild Development|September 1, 2012
A genome-wide association study of autism incorporating autism diagnostic interview-revised, autism diagnostic observation schedule, and social responsiveness scaleJohn J Connolly, Joseph T Glessner, Hakon HakonarsonJournal of Human Genetics|August 28, 2019
Application of ACMG criteria to classify variants in the human gene mutation databaseHui-Qi Qu, Xiang Wang, Lifeng Tian, et al.Discovery Medicine|February 1, 2011
The genetics of asthma and allergic disordersMichael E March, Patrick M A Sleiman, Hakon HakonarsonPageof 91