Linkage of hereditary haemorrhagic telangiectasia to chromosome 9q34 and evidence for locus heterogeneity.

Hereditary haemorrhagic telangiectasia (HHT) is an autosomal dominant disorder with unknown pathophysiology that is characterised by arteriovenous lesions and recurrent haemorrhage in virtually every organ. Linkage of HHT to markers on chromosome 9q has recently been reported. In this study we repor...

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Bibliographic Details
Main Authors: Heutink, P, Haitjema, T, Breedveld, G J, Janssen, B, Sandkuijl, L A, Bontekoe, C J, Westerman, C J, Oostra, B A
Format: Artigo
Language:Inglês
Published: 1994
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Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016693/
https://ncbi.nlm.nih.gov/pubmed/7891375
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