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Translational Research : the Journal of Laboratory and Clinical Medicine|November 21, 2023
High Comorbidity of Pediatric Cancers in Patients with Birth Defects: Insights from Whole Genome Sequencing Analysis of Copy Number VariationsHui-Qi Qu, Joseph T Glessner, Jingchun Qu, et al.Digestive Diseases (Basel, Switzerland)|September 30, 2009
Genetic determinants of pediatric inflammatory bowel disease: is age of onset genetically determined?Rebecca Scherr, Jonah Essers, Hakon Hakonarson, et al.Journal of Immunology (Baltimore, Md. : 1950)|October 2, 2009
A cis-acting regulatory variant in the IL2RA locusHui-Qi Qu, Dominique J Verlaan, Bing Ge, et al.Bioinformatics (Oxford, England)|August 6, 2009
Multiple testing in genome-wide association studies via hidden Markov modelsZhi Wei, Wenguang Sun, Kai Wang, et al.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 HakonarsonPageof 93