-
1
-
-
0023775336
-
Simultaneous gastric cancer in monozygotic twins
-
Matsukura N, Onda M, Tokunaga A, Yoshiyuki T, Shimizu Y, Nishi K, et al. Simultaneous gastric cancer in monozygotic twins. Cancer 1988; 62: 2430-5.
-
(1988)
Cancer
, vol.62
, pp. 2430-2435
-
-
Matsukura, N.1
Onda, M.2
Tokunaga, A.3
Yoshiyuki, T.4
Shimizu, Y.5
Nishi, K.6
-
2
-
-
0028762431
-
The molecular basis of leukemia
-
Cline MJ. The molecular basis of leukemia. N Engl J Med 1994; 330: 328-36.
-
(1994)
N Engl J Med
, vol.330
, pp. 328-336
-
-
Cline, M.J.1
-
4
-
-
0022977531
-
Hereditary gastointestinal polyposis syndromes
-
Haggitt RC, Reid BJ. Hereditary gastointestinal polyposis syndromes. Am J Surg Pathol 1986; 10(12): 871-87.
-
(1986)
Am J Surg Pathol
, vol.10
, Issue.12
, pp. 871-887
-
-
Haggitt, R.C.1
Reid, B.J.2
-
6
-
-
0027482019
-
All in the (cancer) family
-
Knudson AG. All in the (cancer) family. Nature Genet 1993; 5: 103-4.
-
(1993)
Nature Genet
, vol.5
, pp. 103-104
-
-
Knudson, A.G.1
-
7
-
-
0024557049
-
Hereditary cancers disclose a class of cancer genes
-
Knudson AG. Hereditary cancers disclose a class of cancer genes. Cancer 1989; 63: 1888-91.
-
(1989)
Cancer
, vol.63
, pp. 1888-1891
-
-
Knudson, A.G.1
-
8
-
-
0026483890
-
Genetics and cytogenetics of retinoblastoma
-
Cowell JK, Hogg A. Genetics and cytogenetics of retinoblastoma. Cancer Genet Cytogenet 1992; 64: 1-11.
-
(1992)
Cancer Genet Cytogenet
, vol.64
, pp. 1-11
-
-
Cowell, J.K.1
Hogg, A.2
-
9
-
-
0028059816
-
Genetic events in the development of Wilms' tumor
-
Coppes MJ, Haber DA, Grundy PE. Genetic events in the development of Wilms' tumor. N Engl J Med 1994; 331: 586-90.
-
(1994)
N Engl J Med
, vol.331
, pp. 586-590
-
-
Coppes, M.J.1
Haber, D.A.2
Grundy, P.E.3
-
10
-
-
0027528817
-
NFl: A prevalent cause of tumorigenesis in human cancers
-
Seizinger BR. NFl: a prevalent cause of tumorigenesis in human cancers. Nature Genet 1993; 3: 97-9.
-
(1993)
Nature Genet
, vol.3
, pp. 97-99
-
-
Seizinger, B.R.1
-
11
-
-
0027490285
-
Molecular genetic aspects of human cancers: The 1993 Frank Rose Lecture
-
Evans HJ. Molecular genetic aspects of human cancers: the 1993 Frank Rose Lecture. Br J Cancer 1993; 68: 1051-60.
-
(1993)
Br J Cancer
, vol.68
, pp. 1051-1060
-
-
Evans, H.J.1
-
12
-
-
0027489384
-
Clinical implications of the p53 tumor-suppressor gene
-
Harris CC, Hollstein M. Clinical implications of the p53 tumor-suppressor gene. N Engl J Med 1993; 329: 1318-27.
-
(1993)
N Engl J Med
, vol.329
, pp. 1318-1327
-
-
Harris, C.C.1
Hollstein, M.2
-
13
-
-
0027315653
-
p53 and the Li-Fraumeni syndrome
-
Malkin D. p53 and the Li-Fraumeni syndrome. Cancer Genet Cytogenet 1993; 66: 83-92.
-
(1993)
Cancer Genet Cytogenet
, vol.66
, pp. 83-92
-
-
Malkin, D.1
-
14
-
-
0027985697
-
High frequency of germline p53 muta-tions in childhood adrenocortical cancer
-
Wagner J, Portwine C, Rabin K, Leclerc JM, Narod SA, Malkin D. High frequency of germline p53 muta-tions in childhood adrenocortical cancer. J Natl Cancer Inst 1994; 86: 1707-10.
-
(1994)
J Natl Cancer Inst
, vol.86
, pp. 1707-1710
-
-
Wagner, J.1
Portwine, C.2
Rabin, K.3
Leclerc, J.M.4
Narod, S.A.5
Malkin, D.6
-
15
-
-
0026632451
-
Mutation pattern of the p53 gene as a diagnostic marker for multiple hepatocellular carcinoma
-
Oda T, Tsuda H, Scarpa A, Sakamoto M, Hirohashi S. Mutation pattern of the p53 gene as a diagnostic marker for multiple hepatocellular carcinoma. Cancer Res 1992; 52: 3674-8.
-
(1992)
Cancer Res
, vol.52
, pp. 3674-3678
-
-
Oda, T.1
Tsuda, H.2
Scarpa, A.3
Sakamoto, M.4
Hirohashi, S.5
-
16
-
-
0028953478
-
Implications of the p53 tumor-suppressor gene in clinical oncology
-
Chang F, Syrjänen S, Syrjänen K. Implications of the p53 tumor-suppressor gene in clinical oncology. J Clin Oncol 1995; 13: 1009-22.
-
(1995)
J Clin Oncol
, vol.13
, pp. 1009-1022
-
-
Chang, F.1
Syrjänen, S.2
Syrjänen, K.3
-
17
-
-
0029014918
-
A new class of colorectal cancer gene
-
Cawkwell L, Quirke P. A new class of colorectal cancer gene. Gut 1995; 36: 641-3.
-
(1995)
Gut
, vol.36
, pp. 641-643
-
-
Cawkwell, L.1
Quirke, P.2
-
18
-
-
0027158031
-
Clues to the pathogene-sis of familial colorectal cancer
-
Aaltonen LA, Peltomäki P, Leach FS, Sistonen P, Pylkkänen L, Mecklin JP, et al. Clues to the pathogene-sis of familial colorectal cancer. Science 1993; 260: 812-6.
-
(1993)
Science
, vol.260
, pp. 812-816
-
-
Aaltonen, L.A.1
Peltomäki, P.2
Leach, F.S.3
Sistonen, P.4
Pylkkänen, L.5
Mecklin, J.P.6
-
19
-
-
0027485551
-
Genetic mapping of a second locus predisposing to hereditary non-polyposis colon cancer
-
Lindblom A, Tannergärd P, Werelius B, Nordenskjöld M. Genetic mapping of a second locus predisposing to hereditary non-polyposis colon cancer. Nature Genet 1993; 5: 279-82.
-
(1993)
Nature Genet
, vol.5
, pp. 279-282
-
-
Lindblom, A.1
Tannergärd, P.2
Werelius, B.3
Nordenskjöld, M.4
-
20
-
-
0028283423
-
Genetic basis of hereditary nonpolyposis colorectal carcinoma (HNPCC)
-
Peltomäki PT. Genetic basis of hereditary nonpolyposis colorectal carcinoma (HNPCC). Ann Med 1994; 26: 215-9.
-
(1994)
Ann Med
, vol.26
, pp. 215-219
-
-
Peltomäki, P.T.1
-
21
-
-
0029008683
-
GTBP, a 160-Kilodalton essential for mismatch-binding activity in human cells
-
Palombo F, Gallinari P, Iaccarino I, Lettieri T, Hughes M, D'Arrigo S, et al. GTBP, a 160-Kilodalton essential for mismatch-binding activity in human cells. Science 1995; 268: 1912-4.
-
(1995)
Science
, vol.268
, pp. 1912-1914
-
-
Palombo, F.1
Gallinari, P.2
Iaccarino, I.3
Lettieri, T.4
Hughes, M.5
D'Arrigo, S.6
-
22
-
-
0029069972
-
Mutations of GTBP in genetically unstable cells
-
Papadopoulos N, Nicolaides NC, Liu B, Parsons R, Lengauer F, Palombo F, et al. Mutations of GTBP in genetically unstable cells. Science 1995; 268: 1915-7.
-
(1995)
Science
, vol.268
, pp. 1915-1917
-
-
Papadopoulos, N.1
Nicolaides, N.C.2
Liu, B.3
Parsons, R.4
Lengauer, F.5
Palombo, F.6
-
23
-
-
0028226295
-
Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients
-
Aaltonen LA, Peltomäki P, Mecklin JP, Järvinen H, Jass JR, Green JS, et al. Replication errors in benign and malignant tumors from hereditary nonpolyposis colorectal cancer patients. Cancer Res 1994; 54: 1645-8.
-
(1994)
Cancer Res
, vol.54
, pp. 1645-1648
-
-
Aaltonen, L.A.1
Peltomäki, P.2
Mecklin, J.P.3
Järvinen, H.4
Jass, J.R.5
Green, J.S.6
-
24
-
-
0028915223
-
Genetic instability occurs in the majority of young patients with colorectal cancer
-
Liu B, Farrington SM, Petersen GM, Hamilton SR, Parsons R, Papadopoulos N, et al. Genetic instability occurs in the majority of young patients with colorectal cancer. Nature Med 1995; 1: 348-52.
-
(1995)
Nature Med
, vol.1
, pp. 348-352
-
-
Liu, B.1
Farrington, S.M.2
Petersen, G.M.3
Hamilton, S.R.4
Parsons, R.5
Papadopoulos, N.6
-
25
-
-
0028915222
-
Molecular foundations of cancer: New targets for intervention
-
Karp JE, Broder S. Molecular foundations of cancer: new targets for intervention. Nature Med 1995; 1: 309-20.
-
(1995)
Nature Med
, vol.1
, pp. 309-320
-
-
Karp, J.E.1
Broder, S.2
-
26
-
-
0028859671
-
Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability
-
Liu B, Nicolaides NC, Markowitz S, Willson JKV, Parsons RE, Jen J, et al. Mismatch repair gene defects in sporadic colorectal cancers with microsatellite instability. Nature Genet 1995; 9: 48-55.
-
(1995)
Nature Genet
, vol.9
, pp. 48-55
-
-
Liu, B.1
Nicolaides, N.C.2
Markowitz, S.3
Willson, J.K.V.4
Parsons, R.E.5
Jen, J.6
-
27
-
-
0028019398
-
Microsatellite instability: Marker of a mutator phenotype in cancer
-
Loeb LA. Microsatellite instability: marker of a mutator phenotype in cancer. Cancer Res 1994; 54: 5059-63.
-
(1994)
Cancer Res
, vol.54
, pp. 5059-5063
-
-
Loeb, L.A.1
-
28
-
-
0027742295
-
The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer
-
Fishel R, Lescoe MK, Rao MRS, Copeland NG, Jenkins NA, Garber J, et al. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon cancer. Cell 1993; 75: 1027-38.
-
(1993)
Cell
, vol.75
, pp. 1027-1038
-
-
Fishel, R.1
Lescoe, M.K.2
Rao, M.R.S.3
Copeland, N.G.4
Jenkins, N.A.5
Garber, J.6
-
29
-
-
0026210609
-
Causes, relevant mechanisms and prevention of large bowel cancer
-
Weisburger JH. Causes, relevant mechanisms and prevention of large bowel cancer. Sem Oncol 1991; 18: 316-36.
-
(1991)
Sem Oncol
, vol.18
, pp. 316-336
-
-
Weisburger, J.H.1
-
30
-
-
0027155904
-
The biology of colorectal cancer. Implications for pretreatment and follow-up management
-
Boland CR. The biology of colorectal cancer. Implications for pretreatment and follow-up management. Cancer 1993; 71: 4180-6.
-
(1993)
Cancer
, vol.71
, pp. 4180-4186
-
-
Boland, C.R.1
-
32
-
-
74549208765
-
Heredity with reference to carcinoma as shown by the study of the cases examined in the pathological laboratory of the University of Michigan, 1895-1913
-
Warthin AS. Heredity with reference to carcinoma as shown by the study of the cases examined in the pathological laboratory of the University of Michigan, 1895-1913. Arch Intern Med 1913; 12: 546-55.
-
(1913)
Arch Intern Med
, vol.12
, pp. 546-555
-
-
Warthin, A.S.1
-
33
-
-
0021995747
-
Hereditary nonpolyposis colorectal cancer (Lynch syndrome I and II)
-
Lynch HT, Kimberling W, Albano WA, Linch JF, Biscone K, Schuelke JS, et al. Hereditary nonpolyposis colorectal cancer (Lynch syndrome I and II). Cancer 1985; 56: 934-8.
-
(1985)
Cancer
, vol.56
, pp. 934-938
-
-
Lynch, H.T.1
Kimberling, W.2
Albano, W.A.3
Linch, J.F.4
Biscone, K.5
Schuelke, J.S.6
-
34
-
-
0025915010
-
Hereditary nonpolyposis colorectal cancer (Lynch syndrome I and II). Genetics, pathology, natural history and cancer control. Part I
-
Lynch HT, Lanspa S, Smyrk T, Boman B, Watson P, Lynch J. Hereditary nonpolyposis colorectal cancer (Lynch syndrome I and II). Genetics, pathology, natural history and cancer control. Part I. Cancer Genet Cytogenet 1991; 53: 143-60.
-
(1991)
Cancer Genet Cytogenet
, vol.53
, pp. 143-160
-
-
Lynch, H.T.1
Lanspa, S.2
Smyrk, T.3
Boman, B.4
Watson, P.5
Lynch, J.6
-
36
-
-
0023236998
-
Screening for colorectal carcinoma in cancer family syndrome kindreds
-
Mecklin JP, Järvinen JA, Aukee S, Elomaa I, Karjalainen K. Screening for colorectal carcinoma in cancer family syndrome kindreds. Scand J Gastroenterol 1987; 22: 449-53.
-
(1987)
Scand J Gastroenterol
, vol.22
, pp. 449-453
-
-
Mecklin, J.P.1
Järvinen, J.A.2
Aukee, S.3
Elomaa, I.4
Karjalainen, K.5
-
37
-
-
0023513650
-
Frequency of hereditary colorectal carcinoma
-
Mecklin JP. Frequency of hereditary colorectal carcinoma. Gastroenterology 1987; 93: 1021-5.
-
(1987)
Gastroenterology
, vol.93
, pp. 1021-1025
-
-
Mecklin, J.P.1
-
38
-
-
0027177167
-
Identification of hereditary nonpolyposis colorectal cancer in the general population
-
Ponz de Leon M, Sassatelli R, Benatti P, Roncucci L. Identification of hereditary nonpolyposis colorectal cancer in the general population. Cancer 1993; 71: 3493-501.
-
(1993)
Cancer
, vol.71
, pp. 3493-3501
-
-
Ponz De Leon, M.1
Sassatelli, R.2
Benatti, P.3
Roncucci, L.4
-
39
-
-
0027276469
-
Tumor spectrum in hereditary nonpolyposis colorectal cancer (HNPCC) and in families with "suspected HNPCC". a population based study in Northern Italy
-
Benatti P, Sassatelli R, Roncucci L, Pedroni M, Fante R, Di Gregorio C, et al. Tumor spectrum in hereditary nonpolyposis colorectal cancer (HNPCC) and in families with "suspected HNPCC". A population based study in Northern Italy. Int J Cancer 1993; 54: 371-7.
-
(1993)
Int J Cancer
, vol.54
, pp. 371-377
-
-
Benatti, P.1
Sassatelli, R.2
Roncucci, L.3
Pedroni, M.4
Fante, R.5
Di Gregorio, C.6
-
40
-
-
0028276666
-
Clinical and pathological characteristics of sporadic colorectal carcinomas with DNA replication errors in microsatellite sequences
-
Kim H, Jen J, Vogelstein B, Hamilton SR. Clinical and pathological characteristics of sporadic colorectal carcinomas with DNA replication errors in microsatellite sequences. Am J Pathol 1994; 145: 148-56.
-
(1994)
Am J Pathol
, vol.145
, pp. 148-156
-
-
Kim, H.1
Jen, J.2
Vogelstein, B.3
Hamilton, S.R.4
-
41
-
-
0029078288
-
Genetic instability associated with adenoma to carcinoma progression in hereditary nonpolyposis colon cancer
-
Jacoby RF, Marshall DJ, Kailas S, Schlack S, Harms B, Love R. Genetic instability associated with adenoma to carcinoma progression in hereditary nonpolyposis colon cancer. Gastroenterology 1995; 109: 73-82.
-
(1995)
Gastroenterology
, vol.109
, pp. 73-82
-
-
Jacoby, R.F.1
Marshall, D.J.2
Kailas, S.3
Schlack, S.4
Harms, B.5
Love, R.6
-
42
-
-
0024435302
-
Special section: Premalignant conditions of the gastrointestinal tract. Familial adenomatous polyposis
-
Bülow S. Special section: premalignant conditions of the gastrointestinal tract. Familial adenomatous polyposis. Ann Med 1989; 21: 299-307.
-
(1989)
Ann Med
, vol.21
, pp. 299-307
-
-
Bülow, S.1
-
43
-
-
0019202765
-
Gardner's syndrome. Recent developments in research and management
-
Naylor EW, Lebenthal E. Gardner's syndrome. Recent developments in research and management. Dig Dis Sci 1980; 25: 945-59.
-
(1980)
Dig Dis Sci
, vol.25
, pp. 945-959
-
-
Naylor, E.W.1
Lebenthal, E.2
-
44
-
-
0029128339
-
First observation of microadenomas in the ileal mucosa of patients with familial adenomatous polyposis and colectomies
-
Bertoni G, Sassatelli R, Nigrisoli E, Tansini P, Roncucci L, Ponz de Leon M, et al. First observation of microadenomas in the ileal mucosa of patients with familial adenomatous polyposis and colectomies. Gastroenterology 1995; 109: 374-80.
-
(1995)
Gastroenterology
, vol.109
, pp. 374-380
-
-
Bertoni, G.1
Sassatelli, R.2
Nigrisoli, E.3
Tansini, P.4
Roncucci, L.5
Ponz De Leon, M.6
-
45
-
-
0023301321
-
Familial polyposis coli
-
Bülow S. Familial polyposis coli. Danish Med Bull 1987; 34: 1-15.
-
(1987)
Danish Med Bull
, vol.34
, pp. 1-15
-
-
Bülow, S.1
-
46
-
-
0027529405
-
Upper gastrointestinal manifestations in families with hereditary flat adenoma syndrome
-
Lynch HT, Smyrk TC, Lanspa SJ, Jenkins JX, Lynch PM, Cavalieri J, et al. Upper gastrointestinal manifestations in families with hereditary flat adenoma syndrome. Cancer 1993; 71: 2709-14.
-
(1993)
Cancer
, vol.71
, pp. 2709-2714
-
-
Lynch, H.T.1
Smyrk, T.C.2
Lanspa, S.J.3
Jenkins, J.X.4
Lynch, P.M.5
Cavalieri, J.6
-
47
-
-
0024452050
-
Brain tumors in familial adenomatous polyposis
-
Kropilak M, Jagelman DG, Fazio VW, Lavery IL, McGannon E. Brain tumors in familial adenomatous polyposis. Dis Colon Rectum 1989; 32: 778-82.
-
(1989)
Dis Colon Rectum
, vol.32
, pp. 778-782
-
-
Kropilak, M.1
Jagelman, D.G.2
Fazio, V.W.3
Lavery, I.L.4
McGannon, E.5
-
48
-
-
0024238366
-
Peutz-Jeghers syndrome: A clinicopathologic survey of the "Harrisburg family" with a 49-year follow-up
-
Foley TR, McGarrity TJ, Abt AB. Peutz-Jeghers syndrome: a clinicopathologic survey of the "Harrisburg family" with a 49-year follow-up. Gastroenterology 1988; 95: 1535-40.
-
(1988)
Gastroenterology
, vol.95
, pp. 1535-1540
-
-
Foley, T.R.1
McGarrity, T.J.2
Abt, A.B.3
-
49
-
-
33749795968
-
Cowden's disease with extensive gastrointestinal polyposis
-
Marra G, Armelao F, Vecchio FM, Percesepe A, Anti M. Cowden's disease with extensive gastrointestinal polyposis. J Clin Gastroenterol 1993; 16: 1-6.
-
(1993)
J Clin Gastroenterol
, vol.16
, pp. 1-6
-
-
Marra, G.1
Armelao, F.2
Vecchio, F.M.3
Percesepe, A.4
Anti, M.5
-
50
-
-
0001613415
-
Juvenile polyposis: Intramucosal signet-cell adenocarcinoma arising in a polyp at a gastrojejunostomy site
-
Saul SH, Raffensperger E. Juvenile polyposis: intramucosal signet-cell adenocarcinoma arising in a polyp at a gastrojejunostomy site. Surg Pathol 1988; 1: 159-64.
-
(1988)
Surg Pathol
, vol.1
, pp. 159-164
-
-
Saul, S.H.1
Raffensperger, E.2
-
51
-
-
0028061678
-
Hereditary gastrointestinal polyposis and nonpolyposis syndromes
-
Rustgi AK. Hereditary gastrointestinal polyposis and nonpolyposis syndromes. N Engl J Med 1994; 331: 1694-702.
-
(1994)
N Engl J Med
, vol.331
, pp. 1694-1702
-
-
Rustgi, A.K.1
-
52
-
-
0022810104
-
Brief clinical report: Gardner syndrome in a man with an interstitial deletion of 5q
-
Herrera L, Kakati S, Gibas L, Pietrzak E, Sandberg AA. Brief clinical report: Gardner syndrome in a man with an interstitial deletion of 5q. Am J Med Genet 1986 25: 473-6.
-
(1986)
Am J Med Genet
, vol.25
, pp. 473-476
-
-
Herrera, L.1
Kakati, S.2
Gibas, L.3
Pietrzak, E.4
Sandberg, A.A.5
-
53
-
-
0023223410
-
Localization of the gene for familial adenomatous polyposis on chromosome 5
-
Bodmer WF, Bailey CJ, Bodmer J, Bussey HJR, Ellis A, Gorman P, et al. Localization of the gene for familial adenomatous polyposis on chromosome 5. Nature 1987; 328: 614-9.
-
(1987)
Nature
, vol.328
, pp. 614-619
-
-
Bodmer, W.F.1
Bailey, C.J.2
Bodmer, J.3
Bussey, H.J.R.4
Ellis, A.5
Gorman, P.6
-
54
-
-
0025899162
-
Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients
-
Nishisho I, Nakamura Y, Miyoshi Y, Miki Y, Ando H, Horii A, et al. Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients. Science 1991; 253: 665-9.
-
(1991)
Science
, vol.253
, pp. 665-669
-
-
Nishisho, I.1
Nakamura, Y.2
Miyoshi, Y.3
Miki, Y.4
Ando, H.5
Horii, A.6
-
55
-
-
0025938038
-
Identification and characterization of the familial adenomatous polyposis coli gene
-
Groden J, Thliveris A, Samowitz W, Carlson M, Gelbert L, Albertsen H, et al. Identification and characterization of the familial adenomatous polyposis coli gene. Cell 1991; 66: 589-600.
-
(1991)
Cell
, vol.66
, pp. 589-600
-
-
Groden, J.1
Thliveris, A.2
Samowitz, W.3
Carlson, M.4
Gelbert, L.5
Albertsen, H.6
-
56
-
-
0027763498
-
Molecular diagnosis of familial adenomatous polyposis
-
Pozell SM, Petersen GM, Krush AJ, Booker S, Jen J, Giardiello FM, et al. Molecular diagnosis of familial adenomatous polyposis. N Engl J Med 1993; 329: 1982-7.
-
(1993)
N Engl J Med
, vol.329
, pp. 1982-1987
-
-
Pozell, S.M.1
Petersen, G.M.2
Krush, A.J.3
Booker, S.4
Jen, J.5
Giardiello, F.M.6
-
57
-
-
0028213461
-
Familial adenomatous polyposis: Mutation at codon 1309 and early onset of colon cancer
-
Caspari R, Friedl W, Mandl M, Möslem G, Kadmon M, Knapp M, et al. Familial adenomatous polyposis: mutation at codon 1309 and early onset of colon cancer. Lancet 1994; 343: 629-32.
-
(1994)
Lancet
, vol.343
, pp. 629-632
-
-
Caspari, R.1
Friedl, W.2
Mandl, M.3
Möslem, G.4
Kadmon, M.5
Knapp, M.6
-
58
-
-
0025354907
-
Genetic analysis of an inherited predisposition to colon cancer in a family with a variable number of adenomatous polyps
-
Leppert M, Burt R, Hughes JP, Samowitz W, Nakamura Y, Woodward S, et al. Genetic analysis of an inherited predisposition to colon cancer in a family with a variable number of adenomatous polyps. N Engl J Med 1990; 322: 904-8.
-
(1990)
N Engl J Med
, vol.322
, pp. 904-908
-
-
Leppert, M.1
Burt, R.2
Hughes, J.P.3
Samowitz, W.4
Nakamura, Y.5
Woodward, S.6
-
59
-
-
0027417312
-
Germ-line mutations in the first 14 exons of the adenomatous polyposis coli (APC) gene
-
Olschwang S, Laurent-Puig P, Groden J, White R, Thomas G. Germ-line mutations in the first 14 exons of the adenomatous polyposis coli (APC) gene. Am J Hum Genet 1993; 52: 273-9.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 273-279
-
-
Olschwang, S.1
Laurent-Puig, P.2
Groden, J.3
White, R.4
Thomas, G.5
-
60
-
-
0027409892
-
Risk factors for breast cancer development
-
Henderson IC. Risk factors for breast cancer development. Cancer (Suppl) 1993; 71: 2127-40.
-
(1993)
Cancer (Suppl)
, vol.71
, pp. 2127-2140
-
-
Henderson, I.C.1
-
61
-
-
0028279729
-
The significance of family history for patients with carcinoma of the breast
-
Israeli D, Tartter PI, Brower ST, Mizrachy B, Bratton J. The significance of family history for patients with carcinoma of the breast. J Am Coll Surg 1994; 179: 29-32.
-
(1994)
J Am Coll Surg
, vol.179
, pp. 29-32
-
-
Israeli, D.1
Tartter, P.I.2
Brower, S.T.3
Mizrachy, B.4
Bratton, J.5
-
62
-
-
0028307156
-
Genetic epidemiology of breast cancer
-
Thompson WD. Genetic epidemiology of breast cancer. Cancer 1994; 74: 279-87.
-
(1994)
Cancer
, vol.74
, pp. 279-287
-
-
Thompson, W.D.1
-
63
-
-
0028202555
-
Hereditary breast cancer and family cancer syndromes
-
Lynch HT, Lynch J, Conway T, Watson P, Feunteun J, Lenoir G, et al. Hereditary breast cancer and family cancer syndromes. World J Surg 1994; 18: 21-31.
-
(1994)
World J Surg
, vol.18
, pp. 21-31
-
-
Lynch, H.T.1
Lynch, J.2
Conway, T.3
Watson, P.4
Feunteun, J.5
Lenoir, G.6
-
64
-
-
0028149189
-
Li-Fraumeni syndrome
-
Birch JM. Li-Fraumeni syndrome. Eur J Cancer 1994; 30A: 1935-41.
-
(1994)
Eur J Cancer
, vol.30 A
, pp. 1935-1941
-
-
Birch, J.M.1
-
65
-
-
0026502762
-
Natural history and age at onset of hereditary breast cancer
-
Lynch HT, Watson P, Conway TA, Lynch JF. Natural history and age at onset of hereditary breast cancer. Cancer 1992; 69: 1404-7.
-
(1992)
Cancer
, vol.69
, pp. 1404-1407
-
-
Lynch, H.T.1
Watson, P.2
Conway, T.A.3
Lynch, J.F.4
-
66
-
-
0025865691
-
Lhermitte-Duclos disease and Cowden disease: A single phakomatosis
-
Padberg GW, Schot JDL, Vielvoye GJ, Bots GTAM, de Beer FC. Lhermitte-Duclos disease and Cowden disease: a single phakomatosis. Ann Neurol 1991; 29: 517-23.
-
(1991)
Ann Neurol
, vol.29
, pp. 517-523
-
-
Padberg, G.W.1
Schot, J.D.L.2
Vielvoye, G.J.3
Bots, G.T.A.M.4
De Beer, F.C.5
-
67
-
-
0027937925
-
The genetics of familial breast cancer and their practical implications
-
Eeles RA, Stratton MR, Goldgar DE, Easton DF. The genetics of familial breast cancer and their practical implications. Eur J Cancer 1994; 30A: 1383-90.
-
(1994)
Eur J Cancer
, vol.30 A
, pp. 1383-1390
-
-
Eeles, R.A.1
Stratton, M.R.2
Goldgar, D.E.3
Easton, D.F.4
-
68
-
-
0027306104
-
High spontaneous intrachromosomal recombination rates in ataxia telangiectasia
-
Meyn MS. High spontaneous intrachromosomal recombination rates in ataxia telangiectasia. Science 1993; 260: 1327-30.
-
(1993)
Science
, vol.260
, pp. 1327-1330
-
-
Meyn, M.S.1
-
69
-
-
0028073794
-
BRCA1 mutations in primary breast and ovarian carcinomas
-
Futreal PA, Liu Q, Shattuck-Eidens D, Cochran C, Harshman K, Tavtigian S, et al. BRCA1 mutations in primary breast and ovarian carcinomas. Science 1994; 266: 120-2.
-
(1994)
Science
, vol.266
, pp. 120-122
-
-
Futreal, P.A.1
Liu, Q.2
Shattuck-Eidens, D.3
Cochran, C.4
Harshman, K.5
Tavtigian, S.6
-
70
-
-
0028113345
-
A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1
-
Miki Y, Swensen J, Shattuck-Eidens D, Futreal PA, Harshman K, Tavtigian S, et al. A strong candidate for the breast and ovarian cancer susceptibility gene BRCA1. Science 1994; 266: 66-71.
-
(1994)
Science
, vol.266
, pp. 66-71
-
-
Miki, Y.1
Swensen, J.2
Shattuck-Eidens, D.3
Futreal, P.A.4
Harshman, K.5
Tavtigian, S.6
-
71
-
-
0028006563
-
Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13
-
Wooster R, Neuhausen SL, Mangion J, Quirk Y, Ford D, Collins N, et al. Localization of a breast cancer susceptibility gene, BRCA2, to chromosome 13q12-13. Science 1994; 265: 2088-90.
-
(1994)
Science
, vol.265
, pp. 2088-2090
-
-
Wooster, R.1
Neuhausen, S.L.2
Mangion, J.3
Quirk, Y.4
Ford, D.5
Collins, N.6
-
72
-
-
0029034155
-
Rapid detection of BRCA1 mutations by the protein truncation test
-
Hogervorst FBL, Cornelis RS, Bout M, van Vliet M, Oosterwijk JC, Olmer R, et al. Rapid detection of BRCA1 mutations by the protein truncation test. Nature Genet 1995; 10: 208-12.
-
(1995)
Nature Genet
, vol.10
, pp. 208-212
-
-
Hogervorst, F.B.L.1
Cornelis, R.S.2
Bout, M.3
Van Vliet, M.4
Oosterwijk, J.C.5
Olmer, R.6
-
73
-
-
0029281279
-
BRCA1: More than a hereditary breast cancer gene?
-
Boyd J. BRCA1: more than a hereditary breast cancer gene? Nature Genet 1995; 9: 335-6.
-
(1995)
Nature Genet
, vol.9
, pp. 335-336
-
-
Boyd, J.1
-
74
-
-
0017818820
-
Genetic and pathologic findings in á kindred with hereditary sarcoma breast cancer, brain tumors, leukemia, lung, laryngeal and adrenal cortical carcinoma
-
Lynch HT, Mulcahy GM, Harris RE, Guirgis HA, Lynch JF. Genetic and pathologic findings in á kindred with hereditary sarcoma breast cancer, brain tumors, leukemia, lung, laryngeal and adrenal cortical carcinoma. Cancer 1978; 41: 2055-64.
-
(1978)
Cancer
, vol.41
, pp. 2055-2064
-
-
Lynch, H.T.1
Mulcahy, G.M.2
Harris, R.E.3
Guirgis, H.A.4
Lynch, J.F.5
-
75
-
-
0025295852
-
The Li-Fraumeni cancer family syndrome
-
Birch JM. The Li-Fraumeni cancer family syndrome. J Pathol 1990; 161: 1-2.
-
(1990)
J Pathol
, vol.161
, pp. 1-2
-
-
Birch, J.M.1
-
76
-
-
0023803484
-
Cancer families: Human models of susceptibility to neoplasia - The Richard and Hinda Rosenthal Foundation Award Lecture
-
Li FP. Cancer families: human models of susceptibility to neoplasia - the Richard and Hinda Rosenthal Foundation Award Lecture. Cancer Res 1988; 48: 5381-6.
-
(1988)
Cancer Res
, vol.48
, pp. 5381-5386
-
-
Li, F.P.1
-
77
-
-
0023715595
-
A cancer family syndrome in twenty-four kindreds
-
Li FP, Fraumeni Jr JF, Mulvihill JJ, Blattner WA, Dreyfus MG, Tucker MA, et al. A cancer family syndrome in twenty-four kindreds. Cancer Res 1988; 48: 5358-62.
-
(1988)
Cancer Res
, vol.48
, pp. 5358-5362
-
-
Li, F.P.1
Fraumeni Jr., J.F.2
Mulvihill, J.J.3
Blattner, W.A.4
Dreyfus, M.G.5
Tucker, M.A.6
-
78
-
-
0026324439
-
Follow-up study of twenty-four families with Li-Fraumeni syndrome
-
Garber JE, Goldstein AM, Kantor AF, Dreyfus MG, Fraumeni Jr JF, Li FP. Follow-up study of twenty-four families with Li-Fraumeni syndrome. Cancer Res 1991; 51: 6094-7.
-
(1991)
Cancer Res
, vol.51
, pp. 6094-6097
-
-
Garber, J.E.1
Goldstein, A.M.2
Kantor, A.F.3
Dreyfus, M.G.4
Fraumeni Jr., J.F.5
Li, F.P.6
-
79
-
-
0026578534
-
The Li-Fraumeni syndrome: From clinical epidemiology to molecular genetics
-
Strong LC, Williams WR, Tainsky MA. The Li-Fraumeni syndrome: from clinical epidemiology to molecular genetics. Am J Epidemiol 1992; 135: 190-9.
-
(1992)
Am J Epidemiol
, vol.135
, pp. 190-199
-
-
Strong, L.C.1
Williams, W.R.2
Tainsky, M.A.3
-
80
-
-
0028353711
-
Multifactorial analysis of p53 alteration in human cancer: A review
-
Soussi T, Legros Y, Lubin R, Ory K, Schlichtholz B. Multifactorial analysis of p53 alteration in human cancer: a review. Int J Cancer 1994; 57: 1-9.
-
(1994)
Int J Cancer
, vol.57
, pp. 1-9
-
-
Soussi, T.1
Legros, Y.2
Lubin, R.3
Ory, K.4
Schlichtholz, B.5
-
81
-
-
0025633582
-
Germ-line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms
-
Malkin D, Li FP, Strong LC, Fraumeni Jr JF, Nelson CE, Kim DH, et al. Germ-line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms. Science 1990; 250: 1233-8.
-
(1990)
Science
, vol.250
, pp. 1233-1238
-
-
Malkin, D.1
Li, F.P.2
Strong, L.C.3
Fraumeni Jr., J.F.4
Nelson, C.E.5
Kim, D.H.6
-
82
-
-
0025648762
-
Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome
-
Srivastava S, Zou Z, Pirollo K, Blattner W, Chang EH. Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome. Nature 1990; 348: 747-9.
-
(1990)
Nature
, vol.348
, pp. 747-749
-
-
Srivastava, S.1
Zou, Z.2
Pirollo, K.3
Blattner, W.4
Chang, E.H.5
-
83
-
-
0028220688
-
Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-Fraumeni families
-
Birch JM, Hartley AL, Tricker KJ, Prosser J, Condie A, Kelsey AM, et al. Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-Fraumeni families. Cancer Res 1994; 54: 1298-304.
-
(1994)
Cancer Res
, vol.54
, pp. 1298-1304
-
-
Birch, J.M.1
Hartley, A.L.2
Tricker, K.J.3
Prosser, J.4
Condie, A.5
Kelsey, A.M.6
-
84
-
-
0026525839
-
Prevalence and spectrum of germ-line mutations of the p53 gene among patients with sarcoma
-
Toguchida J, Yamaguchi T, Dayton SH, Beauchamp RL, Herrera GE, Ishizaki K, et al. Prevalence and spectrum of germ-line mutations of the p53 gene among patients with sarcoma. N Engl J Med 1992; 326: 1301-8.
-
(1992)
N Engl J Med
, vol.326
, pp. 1301-1308
-
-
Toguchida, J.1
Yamaguchi, T.2
Dayton, S.H.3
Beauchamp, R.L.4
Herrera, G.E.5
Ishizaki, K.6
-
85
-
-
0027265630
-
Patterns of cancer in the families of children with soft tissue sarcoma
-
Hartley AL, Birch JM, Blair V, Kelsey AM, Harris M, Morris Jones PH. Patterns of cancer in the families of children with soft tissue sarcoma. Cancer 1993; 72: 923-30.
-
(1993)
Cancer
, vol.72
, pp. 923-930
-
-
Hartley, A.L.1
Birch, J.M.2
Blair, V.3
Kelsey, A.M.4
Harris, M.5
Morris Jones, P.H.6
-
86
-
-
0027252913
-
Predictive testing for germline mutations in the p53 gene: Are all the questions answered?
-
Eeles RA. Predictive testing for germline mutations in the p53 gene: are all the questions answered? Eur J Cancer 1993; 29A: 1361-5.
-
(1993)
Eur J Cancer
, vol.29 A
, pp. 1361-1365
-
-
Eeles, R.A.1
-
87
-
-
0028077208
-
Von Hippel-Lindau disease
-
Maher ER. von Hippel-Lindau disease. Eur J Cancer 1994; 30A: 1987-90.
-
(1994)
Eur J Cancer
, vol.30 A
, pp. 1987-1990
-
-
Maher, E.R.1
-
89
-
-
0027240519
-
Identification of the von Hippel-Lindau disease tumor suppressor gene
-
Latif F, Tory K, Gnarra J, Yao M, Duh FM, Orcutt ML, et al. Identification of the von Hippel-Lindau disease tumor suppressor gene. Science 1993; 260: 1317-20.
-
(1993)
Science
, vol.260
, pp. 1317-1320
-
-
Latif, F.1
Tory, K.2
Gnarra, J.3
Yao, M.4
Duh, F.M.5
Orcutt, M.L.6
-
90
-
-
0029057487
-
Loss of heterozygosity on the short arm of chromosome 3 in sporadic, von Hippel-Lindau disease-associated, and familial pheochromocytoma
-
Zeiger MA, Zbar B, Keiser H, Marston Linehan W, Gnarra JR. Loss of heterozygosity on the short arm of chromosome 3 in sporadic, von Hippel-Lindau disease-associated, and familial pheochromocytoma. Genes Chromosome Cancer 1995; 13: 151-6.
-
(1995)
Genes Chromosome Cancer
, vol.13
, pp. 151-156
-
-
Zeiger, M.A.1
Zbar, B.2
Keiser, H.3
Marston Linehan, W.4
Gnarra, J.R.5
-
91
-
-
0028235907
-
Frequent somatic mutations and loss of heterozygosity of the von Hippel-Lindau tumor suppressor gene in primary human renal cell carcinomas
-
Shuin T, Kondo K, Torigoe S, Kishida T, Kubota Y, Hosaka M, et al. Frequent somatic mutations and loss of heterozygosity of the von Hippel-Lindau tumor suppressor gene in primary human renal cell carcinomas. Cancer Res 1994; 54: 2852-5.
-
(1994)
Cancer Res
, vol.54
, pp. 2852-2855
-
-
Shuin, T.1
Kondo, K.2
Torigoe, S.3
Kishida, T.4
Kubota, Y.5
Hosaka, M.6
-
92
-
-
0028109496
-
Clinical value of direct DNA analysis of the RET proto-oncogene in families with multiple endocrine neoplasia type 2A
-
Feldman GL, Kambouris M, Talpos GB, Mulligan LM, Ponder BA, Jackson CE. Clinical value of direct DNA analysis of the RET proto-oncogene in families with multiple endocrine neoplasia type 2A. Surgery 1994; 116: 1042-7.
-
(1994)
Surgery
, vol.116
, pp. 1042-1047
-
-
Feldman, G.L.1
Kambouris, M.2
Talpos, G.B.3
Mulligan, L.M.4
Ponder, B.A.5
Jackson, C.E.6
-
93
-
-
0011153988
-
Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma
-
Kovacs G, Erlandsson R, Boldog F, Ingvarsson S, Müller-Brechlin R, Klein G, et al. Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma. Proc Natl Acad Sci 1988; 85: 1571-5.
-
(1988)
Proc Natl Acad Sci
, vol.85
, pp. 1571-1575
-
-
Kovacs, G.1
Erlandsson, R.2
Boldog, F.3
Ingvarsson, S.4
Müller-Brechlin, R.5
Klein, G.6
-
94
-
-
0027282013
-
Chromosome 17p deletions and p53 mutations in renal cell carcinoma
-
Reiter RE, Anglard P, Liu S, Gnarra JR, Marston Linehan W. Chromosome 17p deletions and p53 mutations in renal cell carcinoma. Cancer Res 1993; 53: 3092-7.
-
(1993)
Cancer Res
, vol.53
, pp. 3092-3097
-
-
Reiter, R.E.1
Anglard, P.2
Liu, S.3
Gnarra, J.R.4
Marston Linehan, W.5
-
95
-
-
0029321141
-
Molecular diagnosis
-
Korf B. Molecular diagnosis. N Engl J Med 1995; 332: 1499-502.
-
(1995)
N Engl J Med
, vol.332
, pp. 1499-1502
-
-
Korf, B.1
-
96
-
-
0028911597
-
Human DNA polymorphism
-
Housman D. Human DNA polymorphism. N Engl J Med 1995; 332: 318-20.
-
(1995)
N Engl J Med
, vol.332
, pp. 318-320
-
-
Housman, D.1
|