Results 111 to 120 of about 16,258 (219)
Founder mutation in Lynch syndrome [PDF]
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
core
Decision analysis in the surgical treatment of colorectal cancer due to a mismatch repair detect. [PDF]
Buskens, E. +9 more
core +1 more source
Background: There is a lack of data on familial aggregation of colorectal cancer (CRC) in Iran. We aimed to deter-mine the frequency of hereditary nonpolyposis colorectal cancer (HNPCC) and familial colorectal cancer (FCC) and to determine the frequency ...
Amin Nemati +3 more
doaj
Rare single‐nucleotide variants of MLH1 and MSH2 genes in patients with Lynch syndrome
Background Approximately 5% of colorectal cancers (CRCs) are hereditary. Lynch syndrome (LS), also known as hereditary nonpolyposis colorectal cancer (HNPCC), is the most common form of recognized hereditary CRC.
Seyed Mohsen Mirabdolhosseini +12 more
doaj +1 more source
Molecular screening for hereditary nonpolyposis colorectal cancer in Bulgaria
Kadiyska Tanya +9 more
doaj +1 more source
Muir-Torre Syndrome, a Rare Phenotype of Hereditary Nonpolyposis Colorectal Cancer With Cutaneous Manifestations. [PDF]
Rubay D +5 more
europepmc +1 more source
MLH1-rheMac hereditary nonpolyposis colorectal cancer syndrome in rhesus macaques. [PDF]
Brammer DW +20 more
europepmc +1 more source
Hereditary Nonpolyposis Colorectal Cancer and Cancer Syndromes: Recent Basic and Clinical Discoveries. [PDF]
Chen E, Xu X, Liu T.
europepmc +1 more source

