Human Genome Epidemiology Literature Finder
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Records 1 - 3 (of 3 Records) |
| Query Trace: Disease and ACVR1B[original query] |
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| Exome-wide somatic mutation characterization of small bowel adenocarcinoma. PLoS genetics 2018 Mar 14 (3): e1007200. Hänninen Ulrika A, Katainen Riku, Tanskanen Tomas, Plaketti Roosa-Maria, Laine Riku, Hamberg Jiri, Ristimäki Ari, Pukkala Eero, Taipale Minna, Mecklin Jukka-Pekka, Forsström Linda M, Pitkänen Esa, Palin Kimmo, Välimäki Niko, Mäkinen Netta, Aaltonen Lauri |
| Ensemble genomic analysis in human lung tissue identifies novel genes for chronic obstructive pulmonary disease. Human genomics 2018 Jan 12 (1): 1. Morrow Jarrett D, Cho Michael H, Platig John, Zhou Xiaobo, DeMeo Dawn L, Qiu Weiliang, Celli Bartholome, Marchetti Nathaniel, Criner Gerard J, Bueno Raphael, Washko George R, Glass Kimberly, Quackenbush John, Silverman Edwin K, Hersh Craig |
| Implication of rare genetic variants of NODAL and ACVR1B in congenital heart disease patients from Indian population. Experimental cell research 2021 10 409 (1): 112869. Yadav Manohar Lal, Ranjan Prashant, Das Parimal, Jain Dharmendra, Kumar Ashok, Mohapatra Bhagyalax |
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