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Chest|March 26, 2022
The Role of Genetic Testing in Pulmonary Fibrosis: A Perspective From the Pulmonary Fibrosis Foundation Genetic Testing Work GroupChad A Newton, Justin M Oldham, Carolyn Applegate, et al.American Journal of Medical Genetics. Part A|March 16, 2013
Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotypeRachel D Burnside, John G Pappas, Stephanie Sacharow, et al.Human Genetics|April 7, 2016
De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic featuresVolkan Okur, Megan T Cho, Lindsay Henderson, et al.Journal of Clinical Immunology|July 9, 2020
Deficiency of Adenosine Deaminase 2 (DADA2): Hidden Variants, Reduced Penetrance, and Unusual InheritanceOskar Schnappauf, Qing Zhou, Natalia Sampaio Moura, et al.Pageof 2