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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Bibliografski detalji
Glavni autori: Heutink, P, Haitjema, T, Breedveld, G J, Janssen, B, Sandkuijl, L A, Bontekoe, C J, Westerman, C J, Oostra, B A
Format: Artigo
Jezik:Inglês
Izdano: 1994
Teme:
Research Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC1016693/
https://ncbi.nlm.nih.gov/pubmed/7891375
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