المؤلفون: Stearman, Robert S, Cornelius, Amber R, Lu, Xiao, Conklin, David S, Del Rosario, Mark J, Lowe, Anita M, Elos, Mihret T, Fettig, Lynsey M, Wong, Randall E, Hara, Naoko, Cogan, Joy D, Phillips, John A, Taylor, Matthew R, Graham, Brian B, Tuder, Rubin M, Loyd, James E, Geraci, Mark W

المصدر: American Journal of Respiratory and Critical Care Medicine. 189(9)

مصطلحات موضوعية: Rare Diseases, Human Genome, Genetics, Aetiology, 2.1 Biological and endogenous factors, Cardiovascular, Bone Morphogenetic Protein Receptors, Type II, Case-Control Studies, Cytochrome P-450 Enzyme System, Disease Progression, Familial Primary Pulmonary Hypertension, Female, Haplotypes, Heterozygote, Humans, Hypertension, Pulmonary, Intramolecular Oxidoreductases, Male, Mutation, Polymerase Chain Reaction, Polymorphism, Genetic, lung diseases, pulmonary hypertension, genetic polymorphism, genetic predisposition to disease, Medical and Health Sciences, Respiratory System

وصف الملف: application/pdf

URL الوصول: https://escholarship.org/uc/item/2c40v26w

المؤلفون: Smilan, Lisa E., Conklin, David S.

المصدر: AJOB Neuroscience ; volume 11, issue 1, page 33-35 ; ISSN 2150-7740 2150-7759

الاتاحة: http://dx.doi.org/10.1080/21507740.2019.1704927
https://www.tandfonline.com/doi/pdf/10.1080/21507740.2019.1704927

المؤلفون: Stearman, Robert S., Cornelius, Amber R., Young, Lisa R., Conklin, David S., Mickler, Elizabeth A., Xiao Lu, Hara, Naoko, Fettig, Lynsey M., Phang, Tzu L., Geraci, Mark W.

المصدر: American Journal of Respiratory & Critical Care Medicine; 7/15/2019, Vol. 200 Issue 2, p253-256, 4p, 2 Charts