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Turcot Syndrome Type 2
An autosomal dominant hereditary neoplastic syndrome caused by mutations in the APC gene. It is characterized by the presence of medulloblastoma and…
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National Institutes of Health
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7 relations
APC gene
APC wt Allele
Adenomatous Polyposis Coli
Colorectal Carcinoma
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2006
2006
APC and CTNNB1 mutations are rare in sporadic ependymomas.
Olabisi E Onilude
,
M. Lusher
,
J. Lindsey
,
A. Pearson
,
D. Ellison
,
S. Clifford
Cancer Genetics and Cytogenetics
2006
Corpus ID: 24939673
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