The molecular genetics of hereditary hemorrhagic telangiectasia

Chest

Volumn 111, Issue 6 SUPPL., 1997, Pages 79S-82S

  Marchuk, Douglas A ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVIN; ENDOGLIN; SCLEROPROTEIN; TRANSFORMING GROWTH FACTOR BETA; TRANSFORMING GROWTH FACTOR BETA RECEPTOR;

ANGIODYSPLASIA; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 9Q; CLINICAL FEATURE; CONFERENCE PAPER; EPISTAXIS; GENE MUTATION; GENETIC LINKAGE; LUNG ARTERIOVENOUS SHUNT; MOLECULAR GENETICS; NUCLEIC ACID BASE SUBSTITUTION; PENETRANCE; PREVALENCE; PRIORITY JOURNAL; RENDU OSLER WEBER DISEASE; TELANGIECTASIA; VASCULAR DISEASE;

EID: 0031010078     PISSN: 00123692     EISSN: None     Source Type: Journal    
DOI: 10.1378/chest.111.6_Supplement.79S     Document Type: Conference Paper

References (3)

1. Plauchu H, Bideau A. Epidemiologie et constitution d'un registre de population a propos d'une concentration geographique d'une maladie hereditaire rare. Population 1984; 4-5:765-86
2. Vase P, Grove O. Gastrointestinal lesions in hereditary hemorrhagic telangiectasia. Gastroenterology 1986; 91:1079-83
3. Guttmacher AE, McKinnon WC, Upton MD. Hereditary hemorrhagic telangiectasia: a disorder in search of the genetics community. Am J Med Genet 1994; 52:252-53