Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene

Oncogene

Volumn 19, Issue 13, 2000, Pages 1719-1723

  De Rosa, Marina ^b   Fasano, Carlo ^b   Panariello, Luigi ^b   Scarano, Maria I ^b   Belli, Giulio ^a   Iannelli, Antonio ^a   Ciciliano, Fabio ^a   Izzo, Paola ^a  

^a UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^b NONE

Author keywords

Brain and olorectal tumors; Microsatellite instability (MIN); PMS2 gene; Turcot syndrome

Indexed keywords

PROTEIN; TRANSFORMING GROWTH FACTOR BETA;

ADOLESCENT; ADULT; ARTICLE; BASE PAIRING; BRAIN TUMOR; CANCER GENETICS; CLINICAL ARTICLE; COLON CANCER; COLON MUCOSA; COLORECTAL CANCER; CONTROLLED STUDY; DNA REPAIR; EXON; FEMALE; FRAMESHIFT MUTATION; GENE DELETION; GENE MUTATION; GERM LINE; HETEROZYGOTE; HUMAN; HUMAN CELL; MALE; MICROSATELLITE INSTABILITY; ONCOGENE; PHENOTYPE; PRIORITY JOURNAL; RECESSIVE INHERITANCE; TURCOT SYNDROME;

EID: 0001510499     PISSN: 09509232     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.onc.1203447     Document Type: Article

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