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BMP9 mutations cause a vascular-anomaly syndrome with phenotypic overlap with hereditary hemorrhagic telangiectasia.
Wooderchak-Donahue WL, McDonald J, O'Fallon B, Upton PD, Li W, Roman BL, Young S, Plant P, Fülöp GT, Langa C, Morrell NW, Botella LM, Bernabeu C, Stevenson DA, Runo JR, Bayrak-Toydemir P. Wooderchak-Donahue WL, et al. Among authors: roman bl. Am J Hum Genet. 2013 Sep 5;93(3):530-7. doi: 10.1016/j.ajhg.2013.07.004. Epub 2013 Aug 22. Am J Hum Genet. 2013. PMID: 23972370 Free PMC article.
Executive summary of the 11th HHT international scientific conference.
Arthur H, Geisthoff U, Gossage JR, Hughes CC, Lacombe P, Meek ME, Oh P, Roman BL, Trerotola SO, Velthuis S, Wooderchak-Donahue W. Arthur H, et al. Among authors: roman bl. Angiogenesis. 2015 Oct;18(4):511-24. doi: 10.1007/s10456-015-9482-5. Angiogenesis. 2015. PMID: 26391603
ALK1 signaling in development and disease: new paradigms.
Roman BL, Hinck AP. Roman BL, et al. Cell Mol Life Sci. 2017 Dec;74(24):4539-4560. doi: 10.1007/s00018-017-2636-4. Epub 2017 Sep 4. Cell Mol Life Sci. 2017. PMID: 28871312 Free PMC article. Review.
45 results