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References
Dausset J, Cann H, Cohen D, Lathrop M, Lalouel J-M, White, R: Centre d’etude du polymorphisme humaine (CEPH): Collaborative Genetic Mapping of the Human Genome. Genomics 1990;6:575–577
Weissenbach J, Gyapay G, Dib C, Vignal A, Morissette J, Millasseau P, Vaysseix G, Lathrop M: A secondgeneration linkage map of the human genome. Nature 1992;359:794–801
Gyapay G, Morissette J, Vignal A, Dib C, Fizames C, Millasseau P, Marc S, Bernardi B, Lathrop M, Weissenbach J: The 1993–94 Genethon human genetic linkage map. Nature Genetics 1994;7:246–339
Buetow KH, Weber JL, Lundwigsen S, Scherpbier-Heddema T, Duyk GM, Sheffield VC, Wang Z, Murray JC: Integrated human genome-wide maps constructed using the CEPH reference panel. Nature Genetics 1994;6:391–393
Green P, Falls K, Crooks S: Documentation for CRI-MAP, version 2.4; 1989:available from P. Green.
Spurr NK, Cox S, Bryant SP, Attwood J, Robson EB, Shields DC, Steinbrueck T, Jenkins T, Murray JC, Kidd KK et al: The CEPH consortium linkage map of human chromosome 2. Genomics 1992;14:1055–1063
NIH/CEPH collaborative mapping group: A comprehensive genetic linkage map of the human genome. Science 1992;258:67–68
Matise TC, Perlin M, Chakravarti A: Automated construction of genetic linkage maps using an expert system (MULTTMAP): a human genome linkage map. Nature Genetics 1994;6:384–390
Tory K, Schmidt L, Li H, Wie MH, Geil L, Hustad T, Latif F, Lerman M, Zbar B: Linkage map of 175 loci on human chromosome 3. Cytogenet Cell Genet 1994;65: 67.
O’Connell R, Rains D, Wilkie P, Garcia D, Matsunami N, Albertsen H, Weber J, Weissenbach J, White R, Naylor S: A microsatellite geneti cmap for chromosome 3. Cytogenet Cell Genet 1994;65:43.
Collaborative Human Linkage Center, CHLC Report 1(1), 1993.
Naylor SL, Buys CHCM, Carritt B: Report of the 4th international workshop on human chromosome 3 mapping. Cytogenet Cell Genet 1994;65:2–33
Vignal A, Gyapay G, Hazan J, Nguyen S, Dupraz Ch, Cheron N, Becuwe N, Tranchant M, Weissenbach J: Nonradioactive multiplex for genotyping of microsatelite markers. Methods in Molecular Genetics 1993;1:211–221
Banchs I, Bosch A, Guimera J, Lazaro C, Puig A, Estivill X: New Alleles at microsatellite loci in CEPH families mainly arise from somatic mutations in the lymphoblastoid cell lines. Human Mutation 1994;3:365–372
Beckmann JS, Richard I, Hillare D, Broux O, Antignac C, Bois E, Cann H, Cottingham RW, Feingold N, Kalil J, Lathrop GM, Marcadet A, Masset M, Mignard C, Passos-Bueno MR, Pellerain N, Dausset J, Fardeau M, Cohen D: A gene for limb-girdle muscular dystrophy maps to chromosome 15 by linkage. CR. Acad Sci Paris 1991;312:141–148
Voltz A, Boyle JM, Cann HM, Cottingham RW, Orr HT, Ziegler, A. Report of the Second International Workshop on Human Chromosome 6. Genomics 1994;21:464–472.
Helms C, Mishra SK, Burgess AK, Cline SL, Knobloch D, Hing AV, Vergnaud G, Donis-Keller H: A comprehensive genetic linkage map of the human genome. Science 1992;258:67–68
Hill AS, Pratt WS, Attwood J, Robson EB, Swallow DM: Polymorphism of a MUC3 gene and its localisation within a preliminary framework map of chromosome 7. Cytogenet. Cell Genet. 1994;65:68.
Gurreri F, Trask BJ, van den Engh G, Krauss CM, Schinzel A, Pettenati MJ, Shindler D, Dietz-Band J, Vergnaud G, Scherer SW, Tsui LC and Meunke M: Physical mapping of the holoproscencephaly critical region on chromosome 7q36. Nature Genetics 1993;3:247–251
Attwood J, Chiano M, Collins A, Donis-Keller H, Dracopoli N, Fountain J, Falk C, Goudie D, Gusella J, Haines J, Armour JAL, Jeffreys AJ, Kwiatkowski D, Lathrop M, Matise T, Northrup H, Pericak-Vance MA, Phillips J, Retief A, Robson E, Shields D, Slaugenhaupt S, Verganud G, Weber J, Weissenbach J, White R, Yates J, Povey S: The CEPH Consortium Map of Chromosome9. Genomics 1994;19:203–214
Povey S, Haines J: Report on the constitution of human chromosome 9. HGM 93. 1993; In press.
Povey S, Smith M, Haines J, Kwiatkowski D, Fountain J, Bale A, Abbott C, Jackson I, Lawrie M, Hulten M: Report on the first international workshop on human chromosome 9. Ann Hum Genet 1992;56:167–221
Kwiatkowski DJ, Dib C, Slaugenhaupt SA, Povey S, Gusella JF, Haines JL: An index marker map of chromosome 9 provides strong evidence for positive interference. Am J Hum Genet 1993;53:1279–1288
Povey S, Armour J, Farndon P, Haines JL, Knowles M, Olapade F, Pilz A, White JA, Members of the Utah Genome Centre Genetic Marker and Mapping Groups, Kwiatkowski DJ: Report on the 3rd Human Chromosome 9 Workshop. Annals of Hum. Genet. 1994;58:177–200
Mao I, Simpson NE: Report of the committee on the genetic constitution of chromosome 10; in Cuticchia AJ, Pearson PL (eds): Human Gene Mapping 1993. Johns Hopkins U. Press, 1993, pp.387–406.
Arps S, Rodewald A, Schmalenberger B, Carl P, Bressel M, Kastendieck H: Cytogenetic survey of 32 cancers of the prostate. Cancer Genet Cytogenet 1993;66:93–99
Fults D, Pedone C: Deletion mapping of the long arm of chromosome 10 in glioblastoma multiforme. Genes Chrom Cancer 1993;7:173–177
Deloukas P, Dauwerse JG, Moschonas NK, van Ommen GJ, van Loon AP: Three human glutamate dehydrogenase genes (GLUD1, GLUDP2 and GLUDP3) genes are located on chromosome 10q, but are not closely physically linked. Genomics 1993;17:676–681
Tzimagiorgis G, Leversha MA, Chroniary K, Goulielmos G, Sargent CA, Ferguson-Smith M, Moschonas NK: Structure and expression analysis of a novel member of the human glutamate dehydrogenase (GLUD) gene family mapped to chromosome 10pll.2 Hum Genet 1993:91:433–438.
Hunt D et al.: Physical mapping of 38 highly informative genetic markers to 10 intervals of chromosome 11q: integration of the physical and genetic maps. Ann. Hum. Genet. 1994;58:81–85
Craig I, Gemmill R, Kucherlapati R: Report of the first international workshop on human chromosome 12 mapping. Cyt.Cell Genet. 1992;61:243–251
Morton, NE: Parameters of the human genome. Proc Natl Acad Sci, USA 1991;88:7474–7476
Bowcock AM, Gerken SC, Barnes RI, Shiang R, Wang Jabs E, Warren AC, Antonarakis S, Retief AE, Vergnaud G, Leppert M, Lalouel J-M, White RL, Cavalli-Sforza LL: The CEPH consortium linkage map of human chromosome 13: Genomics 1993;16:486–496.
Bowcock A, Osborne-Lawrence S, Barnes R, Chakravarti A, Washington S, Dunn C: Microsatellite polymorphism linkage map of human chromosome 13q. Genomics 1993;15:376–386
Petrukhin KE, Speer MC, Cayanis E, Bonaldo M de F, Tantravahi U, Soares MB, Fischer SG, Warburton D, Gilliam TC, Ott J: A microsatellite genetic linkage map of human chromosome 13. Genomics 1993;15:76–85
Kooy RF, Verlind E, Shapiro DN, Cowell JK, Scheffer H and Buys CHCM: A deletion hybrid breakpoint map of the chromosomal region 13q14-q21 orders 19 genetic markers in ten intervals Eur J Hum Genet 1994;2;59–65.
Cox D, et al.: A linkage map of human chromosome 14 including 12 gene loci. Genomics 1994;in press.
Sarfarazi M, Tsipouras P, Del Mastro R, Kilpatrick M, Farndon P, Boxed M, Bridges A, Boileau C, Junien C, Hayward C, Brock D, Child A: A linkage map of 10 loci flanking the Marfan syndrome locus on 15q: results of an international consortium study. J. Med. Genet. 1992;29:75–80
Bowcock AM, Barnes RI, White RL, Kruse TA, Tsipouras P, Sarfarazi M, Jenkins T, Viljoen C, Litt M, Kramer PL, Murray JC, Vergnaud G: The CEPH consortium linkage map of human chromosome 15q. Genomics 1992;14:833–840
Donlon TJ, Beckmann JS, Malcolm S: Genome Priority Reports 1993;1:438–447.
Fougerousse F, Broux O, Richard R, Allamand V, de Souza A, Bourg N, Brenguier L, Devaud C, Pasturaud P, Roudant C, Channilkulchai N, Hillaire D, Bui H, Chumakov I, Weissenbach J, Cherif D, Cohen D, Beckmann JS. Mapping of a chromosome 15 region involved in limb girdle muscular dystrophy. J S Hum Mol Genet 1994;3:285–293.
Hidebrand CE, Breunig MH, Reeders ST, Callen D: Report of committee on the genetic constitution of chromosome 16 p448-472 Chromosome Coordinating Meeting (1992): Cuticchia AJ, Pearson PL, Klinger HP (eds) Genome Priority Reports vol. 1. Basel Karger, 1993
Solomon E, Ledbetter D, Fain P: Report on the genetic constitution of chromosome 17p473-504 Chromosome Coordinating Meeting (1992): Cuticchia, AJ, Pearson PL, Klinger HP (eds) Genome Priority Reports vol. 1. Basel Karger, 1993.
Donis-Keller H, Green P, Helms C, Cartinhour S, Weiffenbach B, Stephens K, Keith TP, Bowden DW, Smith DR, Lander ES et al: A genetic linkage map of the human genome. Cell 1987;51:319–337
O’Connell P, Lathrop GM, Leppert M, Nakamura Y, Muller U, Lalouel J-M, White R: Twelve loci form a continuous linkage map for human chromosome 18. Genomics 1988;3:367–372
Straub RE, Speer MC, Luo Y, Rojas K, Overhauser J, Ott J, Gilliam TC: A microsatellite genetic linkage map of human chromosome 18. Genomics 1993;15:48–56
Rojas K, Overhauser J: Sublocalization of 21 chromosome 18-specific microsatellite markers. Genomics 1993;18:169–171
Harley HG, Brook JD, Floyd Rundle SA, Crow S, Walsh KV, Thibault MC, Harper PS, Shaw DJ: Detection of linkage disequilibrium between the Myotonic dystrophy locus and a new polymorphic DNA marker. Am J Hum Genet 1991;49:68–75
Shaw DJ, Harley HG, Brook JD, McKeithan TW: Long range restricton map of a region of human chromosome 19 containing the apolipoprotein genes, a CII - associated break point, and two polymorphic MluI sites. Hum Genet. 1989;83:71–74
Hazan J, Dubay C, Pankowiak MP, Becuwe N, Weissenbach J: A genetic linkage map of human chromosome 20 composed entirely of microsatellite markers. Genomics 1992;12:183–189
Melis R, Bradley P, Eisner T, Robertson M, Lawrence E, Gerken S, Albertsen H, White R: Polymorphic SSR (Simple-Sequence-Repeat) markers for chromosome 20. Genomics 1993;16:56–62
Vergnaud G, Mariat D, Apiou F, Aurias A, Lathrop M, Lauthier V: The use of synthetic tandem repeats to isolate new VNTR loci: cloning of a human hypermutable sequence. Genomics 1991;11:135–144
Lofner C, Rao VVNG, Schnittger S, Pastuszak D, Schubert S, Hansmann I: A first FISH map of human chromosome 20 discloses complete homology with mouse chromosome 2 and assigns candidate mutations. Am J Hum Genet 1993;53:1324.
Mclnnis MG, Chakravarti A, Blaschak J, Petersen MB, Sharma V, Avramopoulos D, Blouin JL, Konig U, Brahe C, Matise TC et al: A linkage map of human chromosome 21: 43 PCR markers at average intervals of 2.5 cM. Genomics 1993;16:562–571
Chumakov I, Rigault P, Guillou S, Ougen P, Billaut A, Guasconi G, Gervy P, LeGall I, Soulare P, Grinas L et al: Continuum of overlapping clones spanning the entire human chromosome 21q. Nature 1992;359:380–387
Bosch A, Nunes V, Patterson D and Estivill X: Isolation and characterisation of fourteen CA-repeat microsatellites from Human Chromosome 21. Genomics 1993;18:151–155
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Spurr, N.K., Bryant, S.P., Attwood, J. et al. European Gene Mapping Project (EUROGEM): Genetic Maps based on the CEPH reference families. Eur J Hum Genet 2, 193–252 (1994). https://doi.org/10.1159/000472364
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DOI: https://doi.org/10.1159/000472364
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