Genetic counseling for hereditary pancreatitis - The role of molecular genetics testing for the cationic trypsinogen gene, cystic fibrosis and serine protease inhibitor Kazal type 1

Gastroenterology Clinics of North America

Volumn 33, Issue 4, 2004, Pages 839-854

  Ellis, Ian ^a  

^a ALDER HEY CHILDREN S HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

APROTININ; SERINE PROTEINASE INHIBITOR; TRYPSINOGEN;

CANCER RISK; CONFERENCE PAPER; CULTURAL FACTOR; DIAGNOSTIC TEST; ENDOCRINE FUNCTION; ENZYME THERAPY; FOLLOW UP; GENE IDENTIFICATION; GENE MUTATION; GENETIC COUNSELING; GENETIC SUSCEPTIBILITY; HEREDITY; HUMAN; MEDICAL ETHICS; MEDICAL SPECIALIST; MOLECULAR GENETICS; PANCREATITIS; RISK ASSESSMENT; TREATMENT INDICATION;

ALGORITHMS; CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR; FEMALE; GENETIC COUNSELING; GENETIC SCREENING; HUMANS; MUTATION; PANCREATIC NEOPLASMS; PANCREATITIS; PREGNANCY; PRENATAL DIAGNOSIS; TRYPSIN; TRYPSIN INHIBITOR, KAZAL PANCREATIC; TRYPSINOGEN;

EID: 7444230399     PISSN: 08898553     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.gtc.2004.07.010     Document Type: Conference Paper

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