How to identify the genetic basis of gastrointestinal and liver diseases?

Gut

Volumn 52, Issue SUPPL. 2, 2003, Pages

  Ferenci, P ^a  

^a MEDICAL UNIVERSITY OF VIENNA   (Austria)

Author keywords

[No Author keywords available]

Indexed keywords

DNA;

CHOLESTASIS; COLON CANCER; COLORECTAL CANCER; CONFERENCE PAPER; CROHN DISEASE; CYSTIC FIBROSIS; DNA POLYMORPHISM; DNA SEQUENCE; DUBIN JOHNSON SYNDROME; FAMILIAL COLON POLYPOSIS; GASTROINTESTINAL DISEASE; GENE MUTATION; GENETIC DISORDER; HEMOCHROMATOSIS; HETEROZYGOSITY LOSS; HUMAN; LIVER DISEASE; MASS SCREENING; MOLECULAR GENETICS; PANCREATITIS; PATHOGENESIS; PENETRANCE; PEUTZ JEGHERS SYNDROME; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SIBLING; WILSON DISEASE;

EID: 0037407528     PISSN: 00175749     EISSN: None     Source Type: Journal    
DOI: 10.1136/gut.52.suppl_2.ii6     Document Type: Conference Paper

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