Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Disease and GDF2[original query] |
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| Clinical and genetic characteristics of pulmonary arterial hypertension in Lebanon. BMC medical genetics 2018 5 19 (1): 89. Abou Hassan Ossama K, Haidar Wiam, Nemer Georges, Skouri Hadi, Haddad Fadi, BouAkl Im |
| Novel risk genes and mechanisms implicated by exome sequencing of 2572 individuals with pulmonary arterial hypertension. Genome medicine 2019 Nov 11 (1): 69. Zhu Na, Pauciulo Michael W, Welch Carrie L, Lutz Katie A, Coleman Anna W, Gonzaga-Jauregui Claudia, Wang Jiayao, Grimes Joseph M, Martin Lisa J, He Hua, , Shen Yufeng, Chung Wendy K, Nichols William |
| Sequence variations of ACVRL1 play a critical role in hepatic vascular malformations in hereditary hemorrhagic telangiectasia. Orphanet journal of rare diseases 2020 9 15 (1): 254. Giraud Sophie, Bardel Claire, Dupuis-Girod Sophie, Carette Marie-France, Gilbert-Dussardier Brigitte, Riviere Sophie, Saurin Jean-Christophe, Eyries Mélanie, Patri Sylvie, Decullier Evelyne, Calender Alain, Lesca Gaët |
| Rare variant analysis of 4241 pulmonary arterial hypertension cases from an international consortium implicates FBLN2, PDGFD, and rare de novo variants in PAH. Genome medicine 2021 May 13 (1): 80. Zhu Na, Swietlik Emilia M, Welch Carrie L, Pauciulo Michael W, Hagen Jacob J, Zhou Xueya, Guo Yicheng, Karten Johannes, Pandya Divya, Tilly Tobias, Lutz Katie A, Martin Jennifer M, Treacy Carmen M, Rosenzweig Erika B, Krishnan Usha, Coleman Anna W, Gonzaga-Jauregui Claudia, Lawrie Allan, Trembath Richard C, Wilkins Martin R, , , , , Morrell Nicholas W, Shen Yufeng, Gräf Stefan, Nichols William C, Chung Wendy |
| [Clinical genetic analysis and diagnosis of a family with hereditary hemorrhagic telangiectasia]. Zhonghua er bi yan hou tou jing wai ke za zhi = Chinese journal of otorhinolaryngology head and neck surgery 2021 12 56 (12): 1307-1312. Song X Y, Yang Y J, Yao Y, Zhang Y, Song X |
| Multiplex Protein Biomarker Profiling in Patients with Familial Hypercholesterolemia. Genes 2021 10 12 (10): . Dlouha Dana, Blaha Milan, Rohlova Eva, Hubacek Jaroslav A, Lanska Vera, Visek Jakub, Blaha Vladim |
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