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1 r who met the Amsterdam criteria for risk of hereditary nonpolyposis colorectal cancer.
2 mimic germline mutations observed for human hereditary nonpolyposis colorectal cancer.
3 hMLH1, hPMS1, and hPMS2 are associated with hereditary nonpolyposis colorectal cancer.
4 tumor testing indicate definite or probable hereditary nonpolyposis colorectal cancer.
5 e MSH2 allele frequency in Lynch syndrome or hereditary nonpolyposis colorectal cancer.
6 in the PMS2 gene are rare in the etiology of hereditary nonpolyposis colorectal cancer.
7 hat defects in MMR predispose individuals to hereditary nonpolyposis colorectal cancer.
8 mmon causes of hereditary diseases including hereditary nonpolyposis colorectal cancer.
9 y three had family histories consistent with hereditary nonpolyposis colorectal cancer.
10 y modify the age at onset of colon cancer in hereditary nonpolyposis colorectal cancer.
11 gene family underlie the MMP, a landmark for hereditary nonpolyposis colorectal cancer.
12 isk for cancer in carriers of a mutation for hereditary nonpolyposis colorectal cancer.
13 many hereditary cancer syndromes, including hereditary nonpolyposis colorectal cancer.
14 ons in human mismatch repair genes result in hereditary nonpolyposis colorectal cancers.
15 s, such as familial adenomatous polyposis or hereditary nonpolyposis colorectal cancer, account for <
16 se the genetic instability characteristic of hereditary nonpolyposis colorectal cancer and a subset o
17 ating the underlying defects responsible for hereditary nonpolyposis colorectal cancer and familial a
18 ysis of two human familial cancer syndromes, hereditary nonpolyposis colorectal cancer and familial a
19 stability (MSI) in tumors from patients with hereditary nonpolyposis colorectal cancer and in a large
20 ch repair (MMR) is found in some hereditary (hereditary nonpolyposis colorectal cancer) and sporadic
21 ents did not meet any published criteria for hereditary nonpolyposis colorectal cancer, and six of th
22 ismatch repair gene MSH2 are associated with hereditary nonpolyposis colorectal cancer as well as a s
23 n human MutS genes cause a predisposition to hereditary nonpolyposis colorectal cancer as well as spo
24 uman cancer susceptibility syndrome known as hereditary nonpolyposis colorectal cancer, as well as so
25 maps to 2p15-2p16.1, a region implicated in hereditary nonpolyposis colorectal cancer, Carney comple
26 In contrast to hereditary nonpolyposis colorectal cancer, characterized
27 ad to the development of the Lynch syndrome (hereditary nonpolyposis colorectal cancer), conferring a
29 l phenotype of Lynch syndrome (also known as hereditary nonpolyposis colorectal cancer) has been well
30 tch repair (MMR) deficiency, which underlies hereditary nonpolyposis colorectal cancer, has recently
32 nked to hMSH2 and also fits the criteria for hereditary nonpolyposis colorectal cancer, having early
33 incidence of rectal cancer in patients with hereditary nonpolyposis colorectal cancer (HNPCC) after
34 aving microsatellite instability, as seen in hereditary nonpolyposis colorectal cancer (HNPCC) and in
36 inherent in mismatch repair (MMR)-deficient hereditary nonpolyposis colorectal cancer (HNPCC) cells.
38 ill Amsterdam criteria for Lynch syndrome or hereditary nonpolyposis colorectal cancer (HNPCC) do not
39 and MLH1 are responsible for the majority of hereditary nonpolyposis colorectal cancer (HNPCC) famili
40 The optimal strategy for the detection of hereditary nonpolyposis colorectal cancer (HNPCC) gene c
43 ensus guidelines for universal screening for hereditary nonpolyposis colorectal cancer (HNPCC) in pat
51 due to hereditary cancer syndromes, of which hereditary nonpolyposis colorectal cancer (HNPCC) is the
53 tations in four DNA mismatch repair genes in hereditary nonpolyposis colorectal cancer (HNPCC) kindre
54 luding familial adenomatous polyposis (FAP), hereditary nonpolyposis colorectal cancer (HNPCC) or Lyn
55 mismatch repair (MMR) gene mutation-negative hereditary nonpolyposis colorectal cancer (HNPCC) patien
57 the colorectal cancer phenotype in multiple hereditary nonpolyposis colorectal cancer (HNPCC) pedigr
58 Mutations in the mismatch repair genes cause hereditary nonpolyposis colorectal cancer (HNPCC) syndro
59 Colorectal cancers arising in patients with hereditary nonpolyposis colorectal cancer (HNPCC) were e
61 on cancer predisposition syndrome in humans, hereditary nonpolyposis colorectal cancer (HNPCC), and a
62 disorder Lynch syndrome (LS), also known as hereditary nonpolyposis colorectal cancer (HNPCC), as we
63 m in colorectal neoplasms from patients with hereditary nonpolyposis colorectal cancer (HNPCC), famil
64 several genetic disorders, including Type I hereditary nonpolyposis colorectal cancer (HNPCC), famil
65 n cases, and the other in autosomal dominant hereditary nonpolyposis colorectal cancer (HNPCC), in wh
66 or hMLH1 mismatch repair gene results in the hereditary nonpolyposis colorectal cancer (HNPCC), or Ly
67 raction with Msh2 and Mlh1, genes that cause hereditary nonpolyposis colorectal cancer (HNPCC), we in
80 ellite instability (MI), a characteristic of hereditary nonpolyposis colorectal cancers (HNPCC) and a
82 the Bethesda guidelines for the diagnosis of hereditary nonpolyposis colorectal cancer (including the
83 r proteins are known to cause instability in hereditary nonpolyposis colorectal cancer, instability t
88 risk for cancer in carriers of mutations for hereditary nonpolyposis colorectal cancer is unclear.
89 ies at high risk for the Lynch syndrome (ie, hereditary nonpolyposis colorectal cancer) is critical f
90 syndromes: familial adenomatosus polyposis, hereditary nonpolyposis colorectal cancer, juvenile poly
91 ) using the panel of markers recommended for hereditary nonpolyposis colorectal cancer kindred and a
92 for tumor development in about half of known hereditary nonpolyposis colorectal cancer kindreds and a
94 mutations of MMR genes in the patients with hereditary nonpolyposis colorectal cancer lead to inacti
95 lts clarify the position of the chromosome 2 hereditary nonpolyposis colorectal cancer locus, which w
96 h repair (MMR) gene MLH1 are associated with hereditary nonpolyposis colorectal cancer (Lynch syndrom
97 vide a molecular framework for understanding hereditary nonpolyposis colorectal cancer mutations and
98 cancer is associated most commonly with the hereditary nonpolyposis colorectal cancer or familial ad
99 the Knudson principle, PMS2 mutations cause hereditary nonpolyposis colorectal cancer or Turcot synd
100 ual absence of clinical premonitory signs in hereditary nonpolyposis colorectal cancer (or Lynch synd
102 cted novel mutations in MLH1 in each of four hereditary nonpolyposis colorectal cancer patients.
103 omes include familial adenomatous polyposis, hereditary nonpolyposis colorectal cancer, Peutz-Jeghers
105 been described in tumors from patients with hereditary nonpolyposis colorectal cancer, sporadic colo
106 commonly seen in tumors associated with the hereditary nonpolyposis colorectal cancer syndrome and i
108 as a screening criterion for Lynch syndrome (hereditary nonpolyposis colorectal cancer syndrome).
109 llite instability (MSI-H) is the hallmark of hereditary nonpolyposis colorectal cancer syndrome, and
110 common type of extracolonic neoplasia in the hereditary nonpolyposis colorectal cancer syndrome, but
111 h as the hereditary breast cancer syndromes, hereditary nonpolyposis colorectal cancer syndrome, Peut
113 ous study demonstrated that in families with hereditary nonpolyposis colorectal cancer, the age of on
114 disease, familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer, together acco
116 fe expectancy for carriers of a mutation for hereditary nonpolyposis colorectal cancer, with benefits
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