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Volumn 131, Issue 4, 2007, Pages 984-987

Long-term outcome in a patient with pulmonary hypertension and hereditary hemorrhagic telangiectasia

Author keywords

Genetic; Hereditary hemorrhagic telangiectasia; Pulmonary hypertension; Pulmonary vascular disease; Shunt

Indexed keywords

BERAPROST; BOSENTAN; CALCIUM CHANNEL BLOCKING AGENT; ILOPROST; NIFEDIPINE; PROSTACYCLIN; UNIPROST; WARFARIN;

EID: 34247198542     PISSN: 00123692     EISSN: None     Source Type: Journal    
DOI: 10.1378/chest.06-2275     Document Type: Article
Times cited : (14)

References (10)
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  • 2
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  • 4
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  • 5
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    • On behalf of the French Rendu-Osler Network: Distribution of ENG and ACVRL1 (ALK1) mutations in French HHT-patients [abstract]
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    • Lesca, G.1    Burnichon, N.2    Raux, G.3
  • 6
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    • Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): Correlation of genotype with phenotype
    • Bossler AD, Richards J, George C, et al. Novel mutations in ENG and ACVRL1 identified in a series of 200 individuals undergoing clinical genetic testing for hereditary hemorrhagic telangiectasia (HHT): correlation of genotype with phenotype. Hum Mutat 2006; 27:667-675
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.