Low prevalence of loss of heterozygosity and SMAD4 mutations in sporadic and familial juvenile polyposis syndrome-associated juvenile polyps

American Journal of Gastroenterology

Volumn 99, Issue 10, 2004, Pages 2025-2031

  Fogt, Franz ^a   Brown, Charlotte A ^b   Badizadegan, Kamrari ^b   Zimmerman, Robert L ^b   Odze, Robert ^b  

^a PENN PRESBYTERIAN MEDICAL CENTER   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

APC PROTEIN; PROTEIN P53; SMAD4 PROTEIN;

ADOLESCENT; ADULT; ARTICLE; CHILD; CHROMOSOME 3P; CHROMOSOME 9P; CHROMOSOME MICRODISSECTION; COLON CARCINOGENESIS; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; DIAGNOSTIC VALUE; DISEASE ASSOCIATION; EPITHELIUM DYSPLASIA; EVALUATION; EXON; FAMILIAL JUVENILE POLYPOSIS SYNDROME; FAMILIAL JUVENILE POLYPOSIS SYNDROME ASSOCIATED JUVENILE POLYP; FAMILIAL POLYPOSIS; FAMILY HISTORY; FEMALE; GENE MUTATION; HETEROZYGOSITY LOSS; HISTOPATHOLOGY; HUMAN; HUMAN TISSUE; INFANT; JUVENILE POLYP; MAJOR CLINICAL STUDY; MALE; MALIGNANT TRANSFORMATION; MUTATIONAL ANALYSIS; POLYMERASE CHAIN REACTION; PREVALENCE; PRIORITY JOURNAL; SENSITIVITY AND SPECIFICITY; SPORADIC JUVENILE POLYP;

ADENOMATOUS POLYPOSIS COLI; ADOLESCENT; ADULT; AGE FACTORS; CHILD; CHILD, PRESCHOOL; DNA-BINDING PROTEINS; FEMALE; HUMANS; INFANT; LOSS OF HETEROZYGOSITY; MALE; MUTATION; PREVALENCE; SMAD4 PROTEIN; TRANS-ACTIVATORS;

EID: 7044264908     PISSN: 00029270     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1572-0241.2004.30502.x     Document Type: Article

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