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Evidence for the founder effect of a novel ACVRL1 splice-site mutation in Hungarian hereditary hemorrhagic telangiectasia families. [electronic resource] by
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In:
Clinical genetics vol. 90
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Human genetics vol. 116
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Report of two FOP cases with 617G>A mutation in the ACVR1 gene from Chinese population. [electronic resource] by
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Producer: 20110103
In:
Clinical dysmorphology vol. 19
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