-
1
-
-
0034089945
-
Cancer risk and low-penetrance susceptibility genes in gene-environment interactions
-
Shields PG, Harris CC. Cancer risk and low-penetrance susceptibility genes in gene-environment interactions. J Clin Oncol 2000;18:2309-15.
-
(2000)
J Clin Oncol
, vol.18
, pp. 2309-2315
-
-
Shields, P.G.1
Harris, C.C.2
-
2
-
-
0032565543
-
Variation in DNA repair is a factor in cancer susceptibility: A paradigm for the promise and perils of individuals and population risk estimation?
-
Mohrenweiser HW, Jones IM. Variation in DNA repair is a factor in cancer susceptibility: a paradigm for the promise and perils of individuals and population risk estimation? Mutat Res 1998;400:15-24.
-
(1998)
Mutat Res
, vol.400
, pp. 15-24
-
-
Mohrenweiser, H.W.1
Jones, I.M.2
-
4
-
-
0036270993
-
DNA repair/pro-apoptotic dual role proteins in five major DNA repair pathways: Fail-safe protection against carcinogenesis
-
Bernstein C, Bernstein H, Payne CM, et al. DNA repair/pro-apoptotic dual role proteins in five major DNA repair pathways: fail-safe protection against carcinogenesis. Mutat Res 2002;511:145-78.
-
(2002)
Mutat Res
, vol.511
, pp. 145-178
-
-
Bernstein, C.1
Bernstein, H.2
Payne, C.M.3
-
7
-
-
0036165623
-
Polymorphisms of the DNA repair gene XRCC1 and risk of primary lung cancer
-
Park JY, Lee SY, Jeon HS, et al. Polymorphisms of the DNA repair gene XRCC1 and risk of primary lung cancer. Cancer Epidemiol Biomarkers Prev 2002;11:23-7.
-
(2002)
Cancer Epidemiol Biomarkers Prev
, vol.11
, pp. 23-27
-
-
Park, J.Y.1
Lee, S.Y.2
Jeon, H.S.3
-
8
-
-
0036119945
-
Lys751Gln polymorphism of the DNA repair gene XPD and risk of primary lung cancer
-
Park JY, Lee SY, Jeon H-S, et al. Lys751Gln polymorphism of the DNA repair gene XPD and risk of primary lung cancer. Lung Cancer 2002;36:15-6.
-
(2002)
Lung Cancer
, vol.36
, pp. 15-16
-
-
Park, J.Y.1
Lee, S.Y.2
Jeon, H.-S.3
-
9
-
-
0036801661
-
Polymorphism of the DNA repair gene XPA and risk of primary lung cancer
-
Park JY, Park SH, Choi JE, et al. Polymorphism of the DNA repair gene XPA and risk of primary lung cancer. Cancer Epidemiol Biomarkers Prev 2002;11:993-7.
-
(2002)
Cancer Epidemiol Biomarkers Prev
, vol.11
, pp. 993-997
-
-
Park, J.Y.1
Park, S.H.2
Choi, J.E.3
-
10
-
-
0028867842
-
Mismatch repair: Mechanisms and relationship to cancer susceptibility
-
Kolodner RD. Mismatch repair: mechanisms and relationship to cancer susceptibility. Trends Biochem Sci 1995;20:397-401.
-
(1995)
Trends Biochem Sci
, vol.20
, pp. 397-401
-
-
Kolodner, R.D.1
-
11
-
-
33646255051
-
Functional interactions and signaling properties of mammalian DNA mismatch repair proteins
-
Bellacosa A. Functional interactions and signaling properties of mammalian DNA mismatch repair proteins. Cell Death Differ 2004;25:1821-7.
-
(2004)
Cell Death Differ
, vol.25
, pp. 1821-1827
-
-
Bellacosa, A.1
-
12
-
-
0036569940
-
Mutations at coding repeat sequences in mismatch repair deficient human cancers: Toward a new concept of target genes for instability
-
Duval A, Hamelin R. Mutations at coding repeat sequences in mismatch repair deficient human cancers: toward a new concept of target genes for instability. Cancer Res 2002;62:2447-54.
-
(2002)
Cancer Res
, vol.62
, pp. 2447-2454
-
-
Duval, A.1
Hamelin, R.2
-
13
-
-
0032997736
-
MLH1 promoter methylation and gene silencing is the primary cause of microsatellite instability in sporadic cancers
-
Simpkins SB, Bocker T, Swisher EM, et al. MLH1 promoter methylation and gene silencing is the primary cause of microsatellite instability in sporadic cancers. Hum Mutat Genet 1999;8:661-6.
-
(1999)
Hum Mutat Genet
, vol.8
, pp. 661-666
-
-
Simpkins, S.B.1
Bocker, T.2
Swisher, E.M.3
-
14
-
-
0032534069
-
A national cancer institute workshop on microsatellite instability for cancer detection and familial predisposition: Development of international criteria for the determination of microsatellite instability in colorectal cancer
-
Boland CR, Thibodeau SN, Hamilton SR, et al. A national cancer institute workshop on microsatellite instability for cancer detection and familial predisposition: development of international criteria for the determination of microsatellite instability in colorectal cancer. Cancer Res 1998;58:5248-57.
-
(1998)
Cancer Res
, vol.58
, pp. 5248-5257
-
-
Boland, C.R.1
Thibodeau, S.N.2
Hamilton, S.R.3
-
15
-
-
0033727894
-
Microsatellite alteration in histologically normal lung tissue of patients with non-small cell lung cancer
-
Park JY, Jeon H-S, Park SH, et al. Microsatellite alteration in histologically normal lung tissue of patients with non-small cell lung cancer. Lung Cancer 2000;30:83-9.
-
(2000)
Lung Cancer
, vol.30
, pp. 83-89
-
-
Park, J.Y.1
Jeon, H.-S.2
Park, S.H.3
-
16
-
-
0033513097
-
Mismatch repair processing of carcinogen-DNA adducts triggers apoptosis
-
Wu J, Gu L, Wang H, et al. Mismatch repair processing of carcinogen-DNA adducts triggers apoptosis. Mol Cell Biol 1999;19:8292-301.
-
(1999)
Mol Cell Biol
, vol.19
, pp. 8292-8301
-
-
Wu, J.1
Gu, L.2
Wang, H.3
-
17
-
-
0032851842
-
Role of DNA mismatch repair and p53 in signaling induction of apoptosis by alkylating agents
-
Hickman MJ, Samson LD. Role of DNA mismatch repair and p53 in signaling induction of apoptosis by alkylating agents. Proc Natl Acad Sci 1999;96:10764-9.
-
(1999)
Proc Natl Acad Sci
, vol.96
, pp. 10764-10769
-
-
Hickman, M.J.1
Samson, L.D.2
-
18
-
-
0029887819
-
Transription-coupled deficiency and mutations in mismatch repair genes
-
Mellon I, Rajpal DK, Koi M, et al. Transription-coupled deficiency and mutations in mismatch repair genes. Science 1996;272:557-60.
-
(1996)
Science
, vol.272
, pp. 557-560
-
-
Mellon, I.1
Rajpal, D.K.2
Koi, M.3
-
19
-
-
0032564458
-
Physical interaction between components of DNA mismatch repair and nucleotide excision repair
-
Bertrand P, Tishkoff DX, Filosi N, et al. Physical interaction between components of DNA mismatch repair and nucleotide excision repair. Proc Natl Acad Sci 1998;95:14278-83.
-
(1998)
Proc Natl Acad Sci
, vol.95
, pp. 14278-14283
-
-
Bertrand, P.1
Tishkoff, D.X.2
Filosi, N.3
-
20
-
-
0028845722
-
Somatic mutations in the hMSH2 gene in microsatellite unstable colorectal carcinomas
-
Borresen AL, Lothe RA, Meling GI, et al. Somatic mutations in the hMSH2 gene in microsatellite unstable colorectal carcinomas. Hum Mol Genet 1995;4:2065-72.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 2065-2072
-
-
Borresen, A.L.1
Lothe, R.A.2
Meling, G.I.3
-
21
-
-
0029991682
-
Microsatellite instability and the role of hMSH2 in sporadic colorectal cancer
-
Bubb VJ, Curtis LJ, Cunningham C, et al. Microsatellite instability and the role of hMSH2 in sporadic colorectal cancer. Oncogene 1996;12:2641-9.
-
(1996)
Oncogene
, vol.12
, pp. 2641-2649
-
-
Bubb, V.J.1
Curtis, L.J.2
Cunningham, C.3
-
22
-
-
0030768854
-
Hereditary nonpolyposis colorectal cancer (HNPCC): Eight germline mutations in hMSH2 or hMLH1 genes
-
Wehner M, Buschhausen L, Lamberti C, et al. Hereditary nonpolyposis colorectal cancer (HNPCC): eight germline mutations in hMSH2 or hMLH1 genes. Hum Mutat 1997;10:241-4.
-
(1997)
Hum Mutat
, vol.10
, pp. 241-244
-
-
Wehner, M.1
Buschhausen, L.2
Lamberti, C.3
-
23
-
-
0031015440
-
Mutations in MLH1 are more frequent than in MSH2 in sporadic colorectal cancers with microsatellite instability
-
Herfarth KKF, Kodner IJ, Whelan AJ, et al. Mutations in MLH1 are more frequent than in MSH2 in sporadic colorectal cancers with microsatellite instability. Genes Chromosomes Cancer 1997;18:42-9.
-
(1997)
Genes Chromosomes Cancer
, vol.18
, pp. 42-49
-
-
Herfarth, K.K.F.1
Kodner, I.J.2
Whelan, A.J.3
-
24
-
-
0031023545
-
Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer
-
Viel A, Genuardi M, Capozzi E, et al. Characterization of MSH2 and MLH1 mutations in Italian families with hereditary nonpolyposis colorectal cancer. Genes Chromosomes Cancer 1997;18:8-18.
-
(1997)
Genes Chromosomes Cancer
, vol.18
, pp. 8-18
-
-
Viel, A.1
Genuardi, M.2
Capozzi, E.3
-
25
-
-
0031579366
-
Low frequency of hMSH2 mutations in Swedish HNPCC families
-
Wahlberg SS, Nystrom-Lahti M, Kane MF, et al. Low frequency of hMSH2 mutations in Swedish HNPCC families. Int J Cancer 1997;74:134-7.
-
(1997)
Int J Cancer
, vol.74
, pp. 134-137
-
-
Wahlberg, S.S.1
Nystrom-Lahti, M.2
Kane, M.F.3
-
26
-
-
0032525830
-
Promoter analysis of the human mismatch repair gene hMSH2
-
Iwahashi Y, Ito E, Yanagisawa Y, et al. Promoter analysis of the human mismatch repair gene hMSH2. Gene 1998;213:141-7.
-
(1998)
Gene
, vol.213
, pp. 141-147
-
-
Iwahashi, Y.1
Ito, E.2
Yanagisawa, Y.3
-
27
-
-
0033951489
-
Intron splice acceptor site polymorphism in the hMSH2 gene in sporadic and familial colorectal cancer
-
Palicio M, Blanco I, Tortola S, et al. Intron splice acceptor site polymorphism in the hMSH2 gene in sporadic and familial colorectal cancer. Br J Cancer 2000;82:535-7.
-
(2000)
Br J Cancer
, vol.82
, pp. 535-537
-
-
Palicio, M.1
Blanco, I.2
Tortola, S.3
-
28
-
-
0036125079
-
A polymorphism in the hMSH2 gene (gIVS12-6T>C) associated with non-Hodgkin lymphomas
-
Paz-y-Mino C, Perez JC, Fiallo BF, et al. A polymorphism in the hMSH2 gene (gIVS12-6T>C) associated with non-Hodgkin lymphomas. Cancer Genet Cytogenet 2002;133:29-33.
-
(2002)
Cancer Genet Cytogenet
, vol.133
, pp. 29-33
-
-
Paz-y-Mino, C.1
Perez, J.C.2
Fiallo, B.F.3
-
29
-
-
0037051664
-
Prevalence of germline mutations in MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer families from Spain
-
Caldes T, Godino J, de la Hoya M, et al. Prevalence of germline mutations in MLH1 and MSH2 in hereditary nonpolyposis colorectal cancer families from Spain. Int J Cancer 2002;98:774-9.
-
(2002)
Int J Cancer
, vol.98
, pp. 774-779
-
-
Caldes, T.1
Godino, J.2
De La Hoya, M.3
-
30
-
-
0037017768
-
Mutation analysis of MLH1 and MSH2 genes performed by denaturing high-performance liquid chromatography
-
Kurzawski G, Safranow K, Suchy J, et al. Mutation analysis of MLH1 and MSH2 genes performed by denaturing high-performance liquid chromatography. J Biochem Biophys Methods 2002;51:89-100.
-
(2002)
J Biochem Biophys Methods
, vol.51
, pp. 89-100
-
-
Kurzawski, G.1
Safranow, K.2
Suchy, J.3
-
31
-
-
2142690241
-
Novel MLH1 mutations and a novel MSH2 polymorphism identified by SSCP and DHPLC in Portuguese HNPCC families
-
Isidro G, Matos S, Goncalves V, et al. Novel MLH1 mutations and a novel MSH2 polymorphism identified by SSCP and DHPLC in Portuguese HNPCC families. Hum Mutat 2003;22:419-20.
-
(2003)
Hum Mutat
, vol.22
, pp. 419-420
-
-
Isidro, G.1
Matos, S.2
Goncalves, V.3
-
32
-
-
12444329767
-
An intron splice acceptor polymorphism in hMSH2 and risk of leukemia after treatment with chemotherapeutic alkylating agents
-
Worrillow LJ, Travis LB, Smith AG, et al. An intron splice acceptor polymorphism in hMSH2 and risk of leukemia after treatment with chemotherapeutic alkylating agents. Clin Cancer Res 2003;9:3012-20.
-
(2003)
Clin Cancer Res
, vol.9
, pp. 3012-3020
-
-
Worrillow, L.J.1
Travis, L.B.2
Smith, A.G.3
-
33
-
-
0142217429
-
Polymorphism in the hMSH2 gene (gIVS12-6T→C) and risk of non-Hodgkin lymphoma in a Japanese population
-
Hishida A, Matsuo K, Hamajima N, et al. Polymorphism in the hMSH2 gene (gIVS12-6T→C) and risk of non-Hodgkin lymphoma in a Japanese population. Cancer Genet Cytogenet 2003;147:71-4.
-
(2003)
Cancer Genet Cytogenet
, vol.147
, pp. 71-74
-
-
Hishida, A.1
Matsuo, K.2
Hamajima, N.3
-
34
-
-
13844267367
-
DNMT3B polymorphisms and risk of primary lung cancer
-
Lee SJ, Jeon H-S, Jang JS, et al. DNMT3B polymorphisms and risk of primary lung cancer. Carcinogenesis 2005;26:403-9.
-
(2005)
Carcinogenesis
, vol.26
, pp. 403-409
-
-
Lee, S.J.1
Jeon, H.-S.2
Jang, J.S.3
-
35
-
-
20144387124
-
Vascular endothelial growth factor gene polymorphisms and risk of primary lung cancer
-
Lee SJ, Lee SY, Jeon H-S, et al. Vascular endothelial growth factor gene polymorphisms and risk of primary lung cancer. Cancer Epidemiol Biomarkers Prev 2005;14:571-5.
-
(2005)
Cancer Epidemiol Biomarkers Prev
, vol.14
, pp. 571-575
-
-
Lee, S.J.1
Lee, S.Y.2
Jeon, H.-S.3
-
36
-
-
0023796209
-
On measures of gametic disequilibrium
-
Lewontin RC. On measures of gametic disequilibrium. Genetics 1998;120:849-52.
-
(1998)
Genetics
, vol.120
, pp. 849-852
-
-
Lewontin, R.C.1
-
37
-
-
0035071957
-
A new statistical method for haplotype reconstruction from population data
-
Stephens M, Smith MJ, Donnelly P. A new statistical method for haplotype reconstruction from population data. Am J Hum Genet 2001;68:978-89.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 978-989
-
-
Stephens, M.1
Smith, M.J.2
Donnelly, P.3
-
38
-
-
0034660559
-
Searching for genetic determinants in the new millennium
-
Risch NJ. Searching for genetic determinants in the new millennium. Nature 2000;405:847-56.
-
(2000)
Nature
, vol.405
, pp. 847-856
-
-
Risch, N.J.1
-
39
-
-
2942519290
-
SNPs, haplotypes, and cancer: Applications in molecular epidemiology
-
Rebbeck TR, Ambrosone CB, Bell DA, et al. SNPs, haplotypes, and cancer: applications in molecular epidemiology. Cancer Epidemiol Biomarkers Prev 2004;13:681-7.
-
(2004)
Cancer Epidemiol Biomarkers Prev
, vol.13
, pp. 681-687
-
-
Rebbeck, T.R.1
Ambrosone, C.B.2
Bell, D.A.3
-
40
-
-
0020592647
-
Experimental studies in rat lungs on the carcinogenicity and dose-response relationships of eight frequently occurring environmental polyaromatic hydrocarbons
-
Deutsch-Wenzel R, Brune H, Grimmer G, et al. Experimental studies in rat lungs on the carcinogenicity and dose-response relationships of eight frequently occurring environmental polyaromatic hydrocarbons. J Natl Cancer Inst 1983;71:539-44.
-
(1983)
J Natl Cancer Inst
, vol.71
, pp. 539-544
-
-
Deutsch-Wenzel, R.1
Brune, H.2
Grimmer, G.3
-
41
-
-
0027488025
-
Cigarette smoking and adenocarcinoma of the lung: The relevance of nicotine-derived nitrosamines
-
Hoffman D, Rivenson A, Murphy SE, et al. Cigarette smoking and adenocarcinoma of the lung: the relevance of nicotine-derived nitrosamines. J Smoking Relat Disord 1993;4:165-90.
-
(1993)
J Smoking Relat Disord
, vol.4
, pp. 165-190
-
-
Hoffman, D.1
Rivenson, A.2
Murphy, S.E.3
-
42
-
-
0031455937
-
An international literature survey of "IARC group I carcinogens" reported mainstream cigarette smoke
-
Smith CJ, Livingston SO, Doolittle DJ. An international literature survey of "IARC group I carcinogens" reported mainstream cigarette smoke. Food Chem Toxicol 1997;35:1107-30.
-
(1997)
Food Chem Toxicol
, vol.35
, pp. 1107-1130
-
-
Smith, C.J.1
Livingston, S.O.2
Doolittle, D.J.3
-
43
-
-
0032820239
-
Ethnic differences in poly(ADP-ribose) polymerase pseudogene genotype distribution and association with lung cancer risk
-
Gu J, Spitz MR, Yang F, et al. Ethnic differences in poly(ADP-ribose) polymerase pseudogene genotype distribution and association with lung cancer risk. Carcinogenesis 1999;20:1465-9.
-
(1999)
Carcinogenesis
, vol.20
, pp. 1465-1469
-
-
Gu, J.1
Spitz, M.R.2
Yang, F.3
-
44
-
-
0033871166
-
hMLH1 and hMSH2 expression correlates with allelic imbalance on chromosome 3p in non-small cell lung cancer
-
Xinarianos G, Liloglou T, Prime W, et al. hMLH1 and hMSH2 expression correlates with allelic imbalance on chromosome 3p in non-small cell lung cancer. Cancer Res 2000;60:4216-21.
-
(2000)
Cancer Res
, vol.60
, pp. 4216-4221
-
-
Xinarianos, G.1
Liloglou, T.2
Prime, W.3
-
45
-
-
85047688675
-
Inactivation of hMLH1 and hMSH2 by promoter methylation in primary non-small cell lung tumors and matched sputum samples
-
Wang YC, Lu YP, Tseng RC, et al. Inactivation of hMLH1 and hMSH2 by promoter methylation in primary non-small cell lung tumors and matched sputum samples. J Clin Invest 2003;111:887-95.
-
(2003)
J Clin Invest
, vol.111
, pp. 887-895
-
-
Wang, Y.C.1
Lu, Y.P.2
Tseng, R.C.3
-
46
-
-
23044491195
-
Promoter hypermethylation is the predominant mechanism in hMLH1 and hMSH2 deregulation and is a poor prognostic factor in nonsmoking lung cancer
-
Hsu HS, Wen CK, Tang YA, et al. Promoter hypermethylation is the predominant mechanism in hMLH1 and hMSH2 deregulation and is a poor prognostic factor in nonsmoking lung cancer. Clin Cancer Res 2005;11:5410-6.
-
(2005)
Clin Cancer Res
, vol.11
, pp. 5410-5416
-
-
Hsu, H.S.1
Wen, C.K.2
Tang, Y.A.3
-
47
-
-
20044364933
-
EGFR mutations in non-small cell lung cancer: Analysis of a large series of cases and development of a rapid and sensitive method for diagnostic screening with potential implications on pharmacologic treatment
-
Marchetti A, Martella C, Felicioni L, et al. EGFR mutations in non-small cell lung cancer: analysis of a large series of cases and development of a rapid and sensitive method for diagnostic screening with potential implications on pharmacologic treatment. J Clin Oncol 2005;23:857-65.
-
(2005)
J Clin Oncol
, vol.23
, pp. 857-865
-
-
Marchetti, A.1
Martella, C.2
Felicioni, L.3
-
48
-
-
4644274700
-
Mutations and addiction to EGFR: The Achilles "heal" of lung cancers?
-
Gazdar AF, Shigematsu H, Herz J, et al. Mutations and addiction to EGFR: the Achilles "heal" of lung cancers? Trends Mol Med 2004;10:481-6.
-
(2004)
Trends Mol Med
, vol.10
, pp. 481-486
-
-
Gazdar, A.F.1
Shigematsu, H.2
Herz, J.3
-
50
-
-
0034929664
-
Notes from the SNP vs. haplotype front
-
Judson R, Stephens JC. Notes from the SNP vs. haplotype front. Pharmacogenomics 2001;2:7-10.
-
(2001)
Pharmacogenomics
, vol.2
, pp. 7-10
-
-
Judson, R.1
Stephens, J.C.2
-
51
-
-
18544366281
-
The association of XRCC1 haplotypes and chromosomal damage levels in peripheral blood lymphocytes among coke-oven workers
-
Leng S, Cheng J, Zhang L, et al. The association of XRCC1 haplotypes and chromosomal damage levels in peripheral blood lymphocytes among coke-oven workers. Cancer Epidemiol Biomarkers Prev 2005;14:1295-301.
-
(2005)
Cancer Epidemiol Biomarkers Prev
, vol.14
, pp. 1295-1301
-
-
Leng, S.1
Cheng, J.2
Zhang, L.3
-
52
-
-
0029051552
-
A germline substitution in the human MSH2 gene is associated with high-grade dysplasia and cancer in ulcerative colitis
-
Brentnall TA, Rubin CE, Crispin DA, et al. A germline substitution in the human MSH2 gene is associated with high-grade dysplasia and cancer in ulcerative colitis. Gastroenterology 1995;109:151-5.
-
(1995)
Gastroenterology
, vol.109
, pp. 151-155
-
-
Brentnall, T.A.1
Rubin, C.E.2
Crispin, D.A.3
-
53
-
-
33646246575
-
An intronic germline transition in the HPNCC gene hMSH2 is associated with sporadic colorectal cancer
-
Goessl C, Plaschke J, Pistorius S, et al. An intronic germline transition in the HPNCC gene hMSH2 is associated with sporadic colorectal cancer. Eur J Cancer 1997;30A:1550-2.
-
(1997)
Eur J Cancer
, vol.30 A
, pp. 1550-1552
-
-
Goessl, C.1
Plaschke, J.2
Pistorius, S.3
-
54
-
-
0029994784
-
A truncated hMSH2 transcript occurs as a common variant in the population: Implication for genetic diagnosis
-
Xia L, Shen W, Ritacca F, et al. A truncated hMSH2 transcript occurs as a common variant in the population: implication for genetic diagnosis. Cancer Res 1996;56:2289-92.
-
(1996)
Cancer Res
, vol.56
, pp. 2289-2292
-
-
Xia, L.1
Shen, W.2
Ritacca, F.3
-
55
-
-
0030892133
-
Alternative splicing of hMSH2 in normal human tissues
-
Mori Y, Shiwaku H, Fukushige S, et al. Alternative splicing of hMSH2 in normal human tissues. Hum Genet 1997;99:590-5.
-
(1997)
Hum Genet
, vol.99
, pp. 590-595
-
-
Mori, Y.1
Shiwaku, H.2
Fukushige, S.3
-
56
-
-
0031922771
-
Characterization of MLH1 and MSH2 alternative splicing and its relevance to molecular testing of colorectal cancer
-
Genuardi M, Viel A, Bonora D, et al. Characterization of MLH1 and MSH2 alternative splicing and its relevance to molecular testing of colorectal cancer. Hum Genet 1998;102:15-20.
-
(1998)
Hum Genet
, vol.102
, pp. 15-20
-
-
Genuardi, M.1
Viel, A.2
Bonora, D.3
|