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A mapped set of markers for human chromosome 15
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An extended linkage map for human chromosome 10
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Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5
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Nakamura Y, Lathrop M, Leppert M, Dobbes M, Wasumuth J, Wolff E, Carlson M, Fujimoto E, Krapcho K, Woodward S, Burt R, Hughes J, Gardner E, Lalouel J-M, White R (1988f): Localization of the genetic defect in familial adenomatous polyposis within a small region of chromosome 5. Am J Hum Genet 43: 638-644, 1988
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40
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Frequent recombination was observed in the distal end of the long arm of human chromosome 14
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Nakamura Y, Lathrop M, O'Connell P, Leppert M, Lalouel J-M, White R (1989a): Frequent recombination was observed in the distal end of the long arm of human chromosome 14. Genomics 4: 76-81
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41
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A genetic linkage map of markers for human chromosome 20
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The role of the APC (adenomatous polyposis coli) gene in human cancers
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Nakamura Y (1993): The role of the APC (adenomatous polyposis coli) gene in human cancers. Adv Cancer Genet 62: 65-87
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Isolation and mapping of 328 new cosmid markers on human chromosome 8: Construction of a high resolution cytogenetic map of chromosome 8 with 416 markers
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Nakamura Y, Okui K, Takahashi E, Koyama K (1994): Isolation and mapping of 328 new cosmid markers on human chromosome 8: construction of a high resolution cytogenetic map of chromosome 8 with 416 markers. Cytogenet Cell Genet 65: 115-118
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Somatic mutation of the APC gene in gastric cancer: Frequent mutations in very well differentiated adenocarcinoma and signet-ring cell carcinoma
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Nakatsuru S, Yanagisawa A, Ichii S, Tahara E, Kalo Y, Nakamura Y, Horii A (1992): Somatic mutation of the APC gene in gastric cancer: frequent mutations in very well differentiated adenocarcinoma and signet-ring cell carcinoma. Hum Mol Genet 1: 559-563
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A comprehensive genetic linkage map of the human genome
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NIH/CEPH Collaborative Mapping Group (1992): A comprehensive genetic linkage map of the human genome. Science 258: 67-86
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0025899162
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Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients
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Nishisho I, Nakamura Y, Miyoshi Y, Miki Y, Ando H, Horii A, Koyama K, Utsunomiya J, Baba S, Hedge P, Markham A, Krush AJ, Petersen G, Hamilton SR, Nilbert MC, Levy DB, Bryan TM, Preisinger AC, Smith KJ, Su L, Kinzler KW, Vogelstein B (1991): Mutations of chromosome 5q21 genes in FAP and colorectal cancer patients. Science 253: 665-669
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Science
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Markham, A.11
Krush, A.J.12
Petersen, G.13
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Nilbert, M.C.15
Levy, D.B.16
Bryan, T.M.17
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Smith, K.J.19
Su, L.20
Kinzler, K.W.21
Vogelstein, B.22
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47
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0024120348
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Twelve loci form a continuous linkage map for human chromosome 18
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O'Connell P, Lathrop M, Leppert M, Nakamura Y, Muller U, Lalouel J-M, White R (1989a): Twelve loci form a continuous linkage map for human chromosome 18. Genomics 3: 367-372
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Genomics
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White, R.7
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48
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0024572895
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Twenty-eight loci form a continuous linkage map of markers for human chromosome 1
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O'Connell P, Lathrop M, Nakamura Y, Leppert M, Ardinger RH, Murray JL, Lalouel J-M, White R (1989b): Twenty-eight loci form a continuous linkage map of markers for human chromosome 1. Genomics 4: 12-20
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Genomics
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49
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0024762579
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Twenty loci form a continuous linkage map of markers for human chromosome 2
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O'Connell P, Lathrop M, Nakamura Y, Leppert M, Lalouel J-M, White R (1989c): Twenty loci form a continuous linkage map of markers for human chromosome 2. Genomics 5: 738-745
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Genomics
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50
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0024757983
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Characterization of VNTR loci by high-resolution agarose gel electrophoresis: Implications for parentage testing and forensic individualization
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Odelberg SJ, Plaetke R, Eldridge JR, Ballard L, O'Connell P, Nakamura Y, Leppert M, Lalouel J-M, White R (1989): Characterization of VNTR loci by high-resolution agarose gel electrophoresis: implications for parentage testing and forensic individualization. Genomics 5: 915-924
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Genomics
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51
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0025941543
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Allelotype of human ovarian cancer
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Sato T, Saito H, Morita R, Koi S, Lee JH, Nakamura Y (199la): Allelotype of human ovarian cancer. Cancer Res 51: 5118-5121
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Cancer Res
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52
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Accumulation of genetic alterations and progression of primary breast cancer
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Sato T, Akiyama F, Sakamoto G, Kasumi F, Nakamura Y (1991b): Accumulation of genetic alterations and progression of primary breast cancer. Cancer Res 51: 5794-5799
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Cancer Res
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53
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0026728003
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A high resolution cytogenetic map of human chromosome 3: Localization of 292 new cosmid markers by a direct mapping system with fluorescence in situ hybridization
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Takahashi E, Yamakawa K, Nakamura Y, Hori T (1992): A high resolution cytogenetic map of human chromosome 3: localization of 292 new cosmid markers by a direct mapping system with fluorescence in situ hybridization. Genomics 13: 1047-1055
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(1992)
Genomics
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Takahashi, E.1
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0027320808
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A high-resolution cytogenetic map of human chromosome 5: Localization of 206 new cosmid markers by direct R-banding fluorescence in situ hybridization
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Takahashi E, Hitomi S, Koyama K, Nakamura Y (1993a): A high-resolution cytogenetic map of human chromosome 5: localization of 206 new cosmid markers by direct R-banding fluorescence in situ hybridization. Genomics 17: 234-236
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Genomics
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0027437261
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A high-resolution cytogenetic map of human chromosome 12: Localization of 195 new cosmid markers by direct R-banding fluorescence in situ hybridization
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Takahashi E, Koyama K, Hitomi S, Nakamura Y (1993b): A high-resolution cytogenetic map of human chromosome 12: localization of 195 new cosmid markers by direct R-banding fluorescence in situ hybridization. Hum Genet 92: 405-409
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Hum Genet
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0027958173
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A high-resolution cytogenetic map of human chromosome 9: Localization of 203 new cosmid markers by direct R-banding fluorescence in situ hybridization
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Takahashi E, Koyama K, Hitomi A, Itoh H, Nakamura Y (1994a): A high-resolution cytogenetic map of human chromosome 9: localization of 203 new cosmid markers by direct R-banding fluorescence in situ hybridization. Genomics 19: 373-375
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Genomics
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0028961358
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A high-resolution cytogenetic map of human chromosome 2: Localization of 434 cosmid markers by direct R-banding fluorescence in situ hybridization
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Takahashi E, Koyama K, Hirai M, Itoh H, Nakamura Y (1994b): A high-resolution cytogenetic map of human chromosome 2: localization of 434 cosmid markers by direct R-banding fluorescence in situ hybridization. Cytogenet Cell Genet 68: 112-114
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Cytogenet Cell Genet
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58
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0026751502
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Allelotype of non-small cell lung carcinoma-comparison of loss of heterozygosity between squamous cell carcinoma and adenocarcinoma
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Tsuchiya E, Nakamura Y, Weng S, Nakagawa K, Tsuchiya S, Sugano H, Kitagawa T (1992): Allelotype of non-small cell lung carcinoma-comparison of loss of heterozygosity between squamous cell carcinoma and adenocarcinoma. Cancer Res 52: 2478-2481
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(1992)
Cancer Res
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Tsuchiya, E.1
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Kitagawa, T.7
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59
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0024891161
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Linkage maps of human chromosomes
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White R, Lalouel J-M, Leppert M, Lathrop M, Nakamura Y, O'Connell P (1989): Linkage maps of human chromosomes. Genome 31: 1066-1072
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(1989)
Genome
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White, R.1
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61
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0025955422
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I991b: A genetic linkage map of 41 RFLP markers for human chromosome 3
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Yamakawa K, Morita R, Takahashi E, Lathrop M. Nakamura Y (I991b): A genetic linkage map of 41 RFLP markers for human chromosome 3. Genomics 11: 565-572
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Genomics
, vol.11
, pp. 565-572
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Yamakawa, K.1
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