Lv74
5038 积分 2021-12-07 加入
Identification of a novel ENG gene mutation (c.1550_1551dupTG, p.S518*) in a Chinese family with hereditary hemorrhagic telangiectasia
19天前
已完结
Pulmonary arteriovenous malformation in Osler-Weber-Rendu syndrome
20天前
已完结
Clinical and genetic characteristics of Chinese patients with hereditary haemorrhagic telangiectasia-associated pulmonary hypertension
20天前
已完结
Arteriovenous malformations in mice lacking activin receptor-like kinase-1
23天前
已完结
Mutations causing premature termination codons discriminate and generate cellular and clinical variability in HHT
1个月前
已关闭
Mutations causing premature termination codons discriminate and generate cellular and clinical variability in HHT
1个月前
已关闭
Pulmonary vascular phenotype identified in patients with GDF2 (BMP9) or BMP10 variants: an international multicentre study
1个月前
已完结
Neurovascular Manifestations in Pediatric Patients With Hereditary Haemorrhagic Telangiectasia
1个月前
已完结
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