A newborn with hereditary haemorrhagic telangiectasia and an unusually severe phenotype

Bibliographic Details
Main Authors:	L Argyriou, J Wirbelauer, A Dev, I Panchulidze, M Shoukier, U Teske, K Nayernia
Format:	Article
Language:	English
Published:	SMW supporting association (Trägerverein Swiss Medical Weekly SMW) 2008-07-01
Series:	Swiss Medical Weekly
Subjects:	Telangiectasia Epistaxis Heart hypertrophy Gene polymorphisms Mutation OslerWeberRendu
Online Access:	https://www.smw.ch/index.php/smw/article/view/874

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