Controlled 15-year trial on screening for colorectal cancer in families with hereditary nonpolyposis colorectal cancer [PDF]
, 2000 Heikki Järvinen +7 more
openalex +1 more source
Deficient DNA mismatch repair and persistence of SARS-CoV-2 RNA shedding: a case report of hereditary nonpolyposis colorectal cancer with COVID-19 infection. [PDF]
BMC Infect Dis, 2021 Haque F, Lillie P, Haque F, Maraveyas A.
europepmc +1 more source
PLoS ONE, 2014 Aberrant telomere length measured in blood has been associated with increased risk of several cancer types. In the field of hereditary non-polyposis colorectal cancer (CRC), and more particularly in Lynch syndrome, caused by germline mutations in the ...
Nuria Seguí +9 more
doaj +1 more source
Deciding the operation type according to mismatch repair status among hereditary nonpolyposis colorectal cancer patients: should a tailored approach be applied, or does one size fit all? [PDF]
Hered Cancer Clin Pract, 2021 Liao CK +5 more
europepmc +1 more source
Cancer genetics in oncology practice [PDF]
, 2017 Cancer is a genetic disease caused by the progressive accumulation of mutations in critical genes that control cell growth and differentiation. Completion of the Human Genome Project promises to revolutionize the practice of Medicine, especially Oncology
Olopade, O. I., Pichert, G.
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Gynaecological surveillance in high risk women [PDF]
, 2016 Increasing availability of genetic testing and falling costs of the tests suggests that growing numbers of unaffected women will be identified worldwide who are at increased risk of gynaecological malignancies.
Dilley, J, Gentry-Maharaj, A, Menon, U
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GSTM1 Polymorphism Does Not Affect Hereditary Nonpolyposis Colorectal Cancer Age of Onset [PDF]
, 2004 J. Shawn Jones +5 more
openalex +1 more source
Cáncer hereditario: fundamentos genéticos [PDF]
, 2005 Genetic counseling plays a key role in the BRCA1/BRCA2 and hMLH1/hMSH2/hMSH6 testing process. The initial genetic counselling encounter will determine the appropriateness of the test by collecting a detailed family history and determining the likelihood ...
Caldés, Trinidad
core +1 more source
Founder mutation in Lynch syndrome [PDF]
, 2016 El síndrome de Lynch es la más frecuente de las neoplasias colorrectales hereditarias. Se origina por mutaciones germinales deletéreas familia-específicas en los genes que codifican proteínas de reparación del ADN: MLH1 (homólogo humano de mutL), MSH2 y ...
Cajal, Andrea +7 more
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