A pilot survey of cystic fibrosis clinical manifestations in CFTR mutation heterozygotes

Genetic Testing

Volumn 5, Issue 3, 2001, Pages 249-254

  Castellani, Carlo ^a   Quinzii, C ^a   Altieri, S ^a   Mastella, G ^a   Assael, B M ^a  

^a UNIVERSITY HOSPITAL OF VERONA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSMEMBRANE CONDUCTANCE REGULATOR;

ADULT; AGE; AGED; ALLERGIC DISEASE; ARTICLE; BRONCHIECTASIS; CFTR GENE; CLINICAL FEATURE; CONTROLLED STUDY; CYSTIC FIBROSIS; DIABETES MELLITUS; DIAGNOSTIC ACCURACY; FEMALE; FRACTURE; GALLSTONE; GENDER; GENE ISOLATION; GENE MUTATION; GENETIC RISK; HEALTH SURVEY; HETEROZYGOSITY; HETEROZYGOTE; HUMAN; HYPERTENSION; LIVER CIRRHOSIS; LUNG ASPERGILLOSIS; MAJOR CLINICAL STUDY; MALE; NOSE POLYP; PANCREATITIS; SINUSITIS;

ADOLESCENT; ADULT; AGED; CHILD; CYSTIC FIBROSIS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; FEMALE; HETEROZYGOTE; HUMANS; INCIDENCE; ITALY; MALE; MIDDLE AGED; MUTATION; PHENOTYPE; PILOT PROJECTS;

EID: 0035690563     PISSN: 10906576     EISSN: None     Source Type: Journal    
DOI: 10.1089/10906570152742317     Document Type: Article

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