Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 228,398,463 papers from all fields of science
Search
Sign In
Create Free Account
Turcot Syndrome Type 1
An autosomal dominant hereditary neoplastic syndrome caused by mutations in the PMS2, MLH1, or MSH2 genes. It is characterized by the presence of…
Expand
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
12 relations
Colorectal Carcinoma
Colorectal adenomas
Glioblastoma
Hereditary Nonpolyposis Colorectal Cancer
Expand
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2004
2004
Molecular analysis of astrocytoma associated with Turcot syndrome type 1--case report.
H. Okamoto
,
T. Mineta
,
Y. Nakahara
,
M. Ichinose
,
T. Shiraishi
,
K. Tabuchi
Neurologia medico-chirurgica
2004
Corpus ID: 37862612
A 49-year-old man presented with a brain tumor and colon carcinoma. The patient had been treated under diagnoses of hereditary…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE