-
1
-
-
85031595334
-
-
International Collaborative Group-HNPCC database, http:// www.nfdht.nl
-
-
-
-
2
-
-
85031591765
-
-
for MTS [MIM 158320] and HNPCC/Lynch syndrome [MIM 120435 and 120436]
-
Online Mendelian Inheritance in Man (OMIM), http:// www.ncbi.nlm.nih.gov/Omim (for MTS [MIM 158320] and HNPCC/Lynch syndrome [MIM 120435 and 120436])
-
-
-
-
3
-
-
0029775147
-
The genetic basis of Muir-Torre syndrome includes the hMLH1 locus
-
Bapat B, Xia L, Madlensky L, Mitri A, Tonin P, Narod SA, Gallinger S (1996) The genetic basis of Muir-Torre syndrome includes the hMLH1 locus. Am J Hum Genet 59:736-739
-
(1996)
Am J Hum Genet
, vol.59
, pp. 736-739
-
-
Bapat, B.1
Xia, L.2
Madlensky, L.3
Mitri, A.4
Tonin, P.5
Narod, S.A.6
Gallinger, S.7
-
4
-
-
0025878737
-
Muir-Torre syndrome: A case report
-
Bisceglia M, Zenarola P (1991) Muir-Torre syndrome: a case report. Tumori 77:277-281
-
(1991)
Tumori
, vol.77
, pp. 277-281
-
-
Bisceglia, M.1
Zenarola, P.2
-
5
-
-
0030727515
-
Microsatellite instability analysis: A multicenter study for reliability and quality control
-
Bocker T, Diermann J, Friedl W, Gebert J, Holinski-Feder E, Karner-Harnusch J, von Knebel-Doeberitz M, et al (1997) Microsatellite instability analysis: a multicenter study for reliability and quality control. Cancer Res 57:4739-4743
-
(1997)
Cancer Res
, vol.57
, pp. 4739-4743
-
-
Bocker, T.1
Diermann, J.2
Friedl, W.3
Gebert, J.4
Holinski-Feder, E.5
Karner-Harnusch, J.6
Von Knebel-Doeberitz, M.7
-
6
-
-
0022912584
-
Muir-Torre syndrome: Histologic spectrum of sebaceous proliferations
-
Burgdorf WHC, Pitha J, Fahmy A (1986) Muir-Torre syndrome: histologic spectrum of sebaceous proliferations. Am J Dermatopathol 8:202-208
-
(1986)
Am J Dermatopathol
, vol.8
, pp. 202-208
-
-
Burgdorf, W.H.C.1
Pitha, J.2
Fahmy, A.3
-
7
-
-
0025755503
-
Association of sebaceous gland tumors and internal malignancy: The Muir-Torre syndrome
-
Cohen PR, Kohn SR, Kurzrock R (1991) Association of sebaceous gland tumors and internal malignancy: the Muir-Torre syndrome. Am J Med 90:606-613
-
(1991)
Am J Med
, vol.90
, pp. 606-613
-
-
Cohen, P.R.1
Kohn, S.R.2
Kurzrock, R.3
-
8
-
-
0030789051
-
Muir-Torre syndrome: Clinical features and molecular genetic analysis
-
Esche C, Kruse R, Lamberti C, Friedl W, Propping P, Lehmann P, Ruzicka T (1997) Muir-Torre syndrome: clinical features and molecular genetic analysis. Br J Dermatol 136:913-917
-
(1997)
Br J Dermatol
, vol.136
, pp. 913-917
-
-
Esche, C.1
Kruse, R.2
Lamberti, C.3
Friedl, W.4
Propping, P.5
Lehmann, P.6
Ruzicka, T.7
-
9
-
-
0027171303
-
Single-step screening method for the most common mutations in familial adenomatous polyposis
-
Friedl W, Mandl M, Sengteller M (1993) Single-step screening method for the most common mutations in familial adenomatous polyposis. Hum Mol Genet 2:1481-1482
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1481-1482
-
-
Friedl, W.1
Mandl, M.2
Sengteller, M.3
-
10
-
-
0027977985
-
Muir-Torre syndrome: Variant of the cancer family syndrome
-
Hall NR, Williams MAT, Murday VA, Newton JA, Bishop DT (1994) Muir-Torre syndrome: variant of the cancer family syndrome. J Med Genet 31:627-631
-
(1994)
J Med Genet
, vol.31
, pp. 627-631
-
-
Hall, N.R.1
Williams, M.A.T.2
Murday, V.A.3
Newton, J.A.4
Bishop, D.T.5
-
11
-
-
0028910650
-
Muir-Torre syndrome: Diagnostic criteria and review of the literature
-
Hartig C, Stieler W, Stadler R (1995) Muir-Torre syndrome: diagnostic criteria and review of the literature. Hautarzt 46:107-113
-
(1995)
Hautarzt
, vol.46
, pp. 107-113
-
-
Hartig, C.1
Stieler, W.2
Stadler, R.3
-
12
-
-
0028215979
-
Microsatellite instability in Muir-Torre syndrome
-
Honchel R, Halling KC, Schaid DJ, Pittelkow M, Thibodeau SN (1994) Microsatellite instability in Muir-Torre syndrome. Cancer Res 54:1159-1163
-
(1994)
Cancer Res
, vol.54
, pp. 1159-1163
-
-
Honchel, R.1
Halling, K.C.2
Schaid, D.J.3
Pittelkow, M.4
Thibodeau, S.N.5
-
13
-
-
0030747145
-
Reduced frequency of extracolonic cancers in hereditary nonpolyposis colorectal cancer families with monoallelic hMLH1 expression
-
Jäger AC, Bisgaard ML, Myrhøj T, Bernstein I, Rehfeld JF, Nielsen FC (1997) Reduced frequency of extracolonic cancers in hereditary nonpolyposis colorectal cancer families with monoallelic hMLH1 expression. Am J Hum Genet 61: 129-138
-
(1997)
Am J Hum Genet
, vol.61
, pp. 129-138
-
-
Jäger, A.C.1
Bisgaard, M.L.2
Myrhøj, T.3
Bernstein, I.4
Rehfeld, J.F.5
Nielsen, F.C.6
-
14
-
-
0028833856
-
Structure of the human MLH1 locus and analysis of a large hereditary nonpolyposis colorectal carcinoma kindred for mlh1 mutations
-
Kolodner RD, Hall NR, Lipford J, Kane MF, Morrison P, Finan PJ, Burn J, et al (1995) Structure of the human MLH1 locus and analysis of a large hereditary nonpolyposis colorectal carcinoma kindred for mlh1 mutations. Cancer Res 55:242-248
-
(1995)
Cancer Res
, vol.55
, pp. 242-248
-
-
Kolodner, R.D.1
Hall, N.R.2
Lipford, J.3
Kane, M.F.4
Morrison, P.5
Finan, P.J.6
Burn, J.7
-
15
-
-
0028585821
-
Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for MSH2 mutations
-
Kolodner RD, Hall NR, Lipford J, Kane MF, Rao MRS, Morrison P, Wirth L, et al (1994) Structure of the human MSH2 locus and analysis of two Muir-Torre kindreds for MSH2 mutations. Genomics 24:516-526
-
(1994)
Genomics
, vol.24
, pp. 516-526
-
-
Kolodner, R.D.1
Hall, N.R.2
Lipford, J.3
Kane, M.F.4
Rao, M.R.S.5
Morrison, P.6
Wirth, L.7
-
16
-
-
10544255347
-
Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene?
-
Kruse R, Lamberti C, Wang Y, Ruelfs C, Bruns A, Esche C, Lehmann P, et al (1996) Is the mismatch repair deficient type of Muir-Torre syndrome confined to mutations in the hMSH2 gene? Hum Genet 98:747-750
-
(1996)
Hum Genet
, vol.98
, pp. 747-750
-
-
Kruse, R.1
Lamberti, C.2
Wang, Y.3
Ruelfs, C.4
Bruns, A.5
Esche, C.6
Lehmann, P.7
-
17
-
-
0028106776
-
hMSH2 mutations in hereditary non-polyposis colorectal cancer kindreds
-
Liu B, Parsons RE, Hamilton SR, Petersen GM, Lynch HT, Watson P, Markowitz S, et al (1994) hMSH2 mutations in hereditary non-polyposis colorectal cancer kindreds. Cancer Res 54:4590-4594
-
(1994)
Cancer Res
, vol.54
, pp. 4590-4594
-
-
Liu, B.1
Parsons, R.E.2
Hamilton, S.R.3
Petersen, G.M.4
Lynch, H.T.5
Watson, P.6
Markowitz, S.7
-
18
-
-
2942569549
-
Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients
-
Liu B, Parsons R, Papadopoulos N, Nicolaides NC, Lynch HT, Watson P, Jass JR, et al (1996) Analysis of mismatch repair genes in hereditary non-polyposis colorectal cancer patients. Nat Med 2:169-174
-
(1996)
Nat Med
, vol.2
, pp. 169-174
-
-
Liu, B.1
Parsons, R.2
Papadopoulos, N.3
Nicolaides, N.C.4
Lynch, H.T.5
Watson, P.6
Jass, J.R.7
-
19
-
-
0029164415
-
In vitro transcription/ translation assay for the screening of hMLH1 and hMSH2 mutations in familial colon cancer
-
Luce MC, Marra G, Chauhan DP, Laghi L, Carethers JM, Cherian SP, Hawn M, et al (1995) In vitro transcription/ translation assay for the screening of hMLH1 and hMSH2 mutations in familial colon cancer. Gastroenterology 109:1368-1374
-
(1995)
Gastroenterology
, vol.109
, pp. 1368-1374
-
-
Luce, M.C.1
Marra, G.2
Chauhan, D.P.3
Laghi, L.4
Carethers, J.M.5
Cherian, S.P.6
Hawn, M.7
-
20
-
-
0019515269
-
The cancer family syndrome: Rare cutaneous phenotypic linkage of Torre's syndrome
-
Lynch HT, Lynch PM, Pester J, Fusaro RM (1981) The cancer family syndrome: rare cutaneous phenotypic linkage of Torre's syndrome. Arch Intern Med 141:607-611
-
(1981)
Arch Intern Med
, vol.141
, pp. 607-611
-
-
Lynch, H.T.1
Lynch, P.M.2
Pester, J.3
Fusaro, R.M.4
-
21
-
-
0024284028
-
A simple salting out procedure for extracting DNA from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16:1215
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
22
-
-
0031278322
-
Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer
-
Miyaki M, Konishi M, Tanaka K, Kikuchi-Yanoshita R, Muraoka M, Yasuno M, Igari T, et al (1997) Germline mutation of MSH6 as the cause of hereditary nonpolyposis colorectal cancer. Nat Genet 17:271-272
-
(1997)
Nat Genet
, vol.17
, pp. 271-272
-
-
Miyaki, M.1
Konishi, M.2
Tanaka, K.3
Kikuchi-Yanoshita, R.4
Muraoka, M.5
Yasuno, M.6
Igari, T.7
-
24
-
-
0030739106
-
Molecular basis of HNPCC: Mutations of MMR genes
-
Papadopoulos N, Lindblom A (1997) Molecular basis of HNPCC: mutations of MMR genes. Hum Mutat 10:89-99
-
(1997)
Hum Mutat
, vol.10
, pp. 89-99
-
-
Papadopoulos, N.1
Lindblom, A.2
-
25
-
-
0030882381
-
Mutations predisposing to hereditary nonpolyposis colorectal cancer: Database and results of a collaborative study: The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer
-
Peltomäki P, Vasen HF (1997) Mutations predisposing to hereditary nonpolyposis colorectal cancer: database and results of a collaborative study: the International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer. Gastroenterology 113:1146-1158
-
(1997)
Gastroenterology
, vol.113
, pp. 1146-1158
-
-
Peltomäki, P.1
Vasen, H.F.2
-
26
-
-
0029013597
-
The Muir-Torre syndrome: A 25-year retrospect
-
Schwartz RA, Torre DP (1995) The Muir-Torre syndrome: a 25-year retrospect. J Am Acad Dermatol 33:90-104
-
(1995)
J Am Acad Dermatol
, vol.33
, pp. 90-104
-
-
Schwartz, R.A.1
Torre, D.P.2
-
27
-
-
0025848680
-
The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC)
-
Vasen HFA, Mecklin J-P, Meera Khan P, Lynch HT (1991) The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC). Dis Colon Rectum 34:424-425
-
(1991)
Dis Colon Rectum
, vol.34
, pp. 424-425
-
-
Vasen, H.F.A.1
Mecklin, J.-P.2
Meera Khan, P.3
Lynch, H.T.4
-
28
-
-
0029862873
-
Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis
-
Vasen HFA, Wijnen JT, Menko FH, Kleibeuker JH, Taal BG, Griffioen G, Nagengast FM, et al (1996) Cancer risk in families with hereditary nonpolyposis colorectal cancer diagnosed by mutation analysis. Gastroenterology 110:1020-1027
-
(1996)
Gastroenterology
, vol.110
, pp. 1020-1027
-
-
Vasen, H.F.A.1
Wijnen, J.T.2
Menko, F.H.3
Kleibeuker, J.H.4
Taal, B.G.5
Griffioen, G.6
Nagengast, F.M.7
-
29
-
-
0030768854
-
Hereditary non-polyposis colorectal cancer (HNPCC): Eight novel germline mutations in the hMSH2 or hMLH1 genes
-
Wehner M, Buschhausen L, Lamberti C, Kruse R, Caspari R, Propping P, Friedl W (1997) Hereditary non-polyposis colorectal cancer (HNPCC): eight novel germline mutations in the hMSH2 or hMLH1 genes. Hum Mutat 10:241-244
-
(1997)
Hum Mutat
, vol.10
, pp. 241-244
-
-
Wehner, M.1
Buschhausen, L.2
Lamberti, C.3
Kruse, R.4
Caspari, R.5
Propping, P.6
Friedl, W.7
-
30
-
-
16944364360
-
Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations
-
Wijnen J, Khan PM, Vasen H, van der Klift H, Mulder A, van Leeuwen-Cornelisse I, Bakker B, et al (1997) Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations. Am J Hum Genet 61:329-335
-
(1997)
Am J Hum Genet
, vol.61
, pp. 329-335
-
-
Wijnen, J.1
Khan, P.M.2
Vasen, H.3
Van Der Klift, H.4
Mulder, A.5
Van Leeuwen-Cornelisse, I.6
Bakker, B.7
-
31
-
-
0028955451
-
Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis
-
Wijnen J, Vasen H, Khan PM, Menko FH, van der Klift H, van Leeuwen C, van den Broek M, et al (1995) Seven new mutations in hMSH2, an HNPCC gene, identified by denaturing gradient-gel electrophoresis. Am J Hum Genet 56:1060-1066
-
(1995)
Am J Hum Genet
, vol.56
, pp. 1060-1066
-
-
Wijnen, J.1
Vasen, H.2
Khan, P.M.3
Menko, F.H.4
Van Der Klift, H.5
Van Leeuwen, C.6
Van Den Broek, M.7
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