-
1
-
-
0028915802
-
A panel of sub-chromosomal painting libraries representing over 300 regions of the human genome
-
Antonacci R. Marzclla R. Finelli P. Lonoce A, Forabo-sco A, Archidiácono N, Rocchi M: A panel of sub-chromosomal painting libraries representing over 300 regions of the human genome. Cytogenet Cell Genet 68:25-32(1995).
-
(1995)
Cytogenet Cell Genet
, vol.68
, pp. 25-32
-
-
Antonacci, R.1
Marzclla, R.2
Finelli, P.3
Lonoce, A.4
Forabo-Sco, A.5
Archidiácono, N.6
Rocchi, M.7
-
2
-
-
0028710442
-
Preparation of human chromosome painting probes from somatic cell hybrids
-
Choo KHA (ed), Humana Press, Ottawa
-
Archidiácono N. Antonacci R. Forabosco A. Rocci M: Preparation of human chromosome painting probes from somatic cell hybrids, in Choo KHA (ed): Methods in Molecular Biology: In situ Hybridization Protocols, pp 1-13 (Humana Press, Ottawa 1994).
-
(1994)
Methods In Molecular Biology: In Situ Hybridization Protocols
, pp. 1-13
-
-
Archidiácono, N.1
Antonacci, R.2
Forabosco, A.3
Rocci, M.4
-
3
-
-
0025973822
-
Ward. DC: In situ hybridisations of human chromosomes with. I/u-PCR products: A simultaneous karyotype for gene mapping stydies
-
Baldini A. Ward. DC: In situ hybridisations of human chromosomes with. I/u-PCR products: a simultaneous karyotype for gene mapping stydies. Genomics 9:770-774 (1991).
-
(1991)
Genomics
, vol.9
, pp. 770-774
-
-
Baldini, A.1
-
4
-
-
0029653653
-
A YAC contig map of the human genome
-
Chumakov IM, Rigault P, Bdlanné-Chantelot C, Billault T, Guillou S, Soularue P, Guasconi G, Poullier E, Belova M, Santbucy J, Susini L, Gcrvy P, Glibert F, Beauftls S, Bui H, Massart C, De Tand MF, Dukasz F, Lckoulanl S, Ougen Y, Perrot V, Saumier M, Soravito C, Bahouayila R, Cohen-Akenine A, Berillot T, Bertrand S, Codani JJ, Caterina D, Georges I, Lacroix B, Lucotte G, Sahbatou M,: A YAC contig map of the human genome. Nature 377(suppl): 175-297 (1995).
-
(1995)
Nature
, vol.377
, pp. 175-297
-
-
Chumakov, I.M.1
Rigault, P.2
Bdlanné-Chantelot, C.3
T, B.4
Guillou, S.5
Soularue, P.6
Guasconi, G.7
Poullier, E.8
Belova, M.9
Santbucy, J.10
Susini, L.11
Gcrvy, P.12
Glibert, F.13
Beauftls, S.14
Bui, H.15
Massart, C.16
De Tand, M.F.17
Dukasz, F.18
Lckoulanl, S.19
Ougen, Y.20
Perrot, V.21
Saumier, M.22
Soravito, C.23
Bahouayila, R.24
Cohen-Akenine, A.25
Berillot, T.26
Bertrand, S.27
Codani, J.J.28
Caterina, D.29
Georges, I.30
Lacroix, B.31
Lucotte, G.32
Sahbatou, M.33
more..
-
5
-
-
12644260443
-
European Gene Mapping Project (EURO-GEM): Breakpoint panels for human chromosomes based on ihe CEPH reference families
-
Cox SA, Attwood J. Bryant SP, Bains R, Povey S. Rcbello M. Kapsctaki M. Moschonas NK. Grzes-chik KH. Otto M, Dixon M. Sudworth HE. Kooy RF. Wright A. Teague P. Terrenalo L, Vergnaud G, Monfouilloux S. Weissenbach J. European Gene Mapping Project (EURO-GEM): breakpoint panels for human chromosomes based on ihe CEPH reference families. Ann hum Genet 60:447-486 (1996).
-
(1996)
Ann Hum Genet
, vol.60
, pp. 447-486
-
-
Cox, S.A.1
Attwood, J.2
Bryant, S.P.3
Bains, R.4
Povey, S.5
Rcbello, M.6
Kapsctaki, M.7
Moschonas, N.K.8
Grzes-Chik, K.H.9
Otto, M.10
Dixon, M.11
Sudworth, H.E.12
Kooy, R.F.13
Wright, A.14
Teague, P.15
Terrenalo, L.16
Vergnaud, G.17
Monfouilloux, S.18
Weissenbach, J.19
-
6
-
-
15844403609
-
A common region of lOp deleted in DiGcorge and velocardiofacial syndromes
-
Daw SC. Taylor C. Kraman M. Call K. Mao J. Schuf-fenhauer S, Meitinger T, Lipson T. Goodship J, Scrambler P: A common region of lOp deleted in DiGcorge and velocardiofacial syndromes. Nature Genet 13:458-460(1996).
-
(1996)
Nature Genet
, vol.13
, pp. 458-460
-
-
Daw, S.C.1
Taylor, C.2
Kraman, M.3
Call, K.4
Mao, J.5
Schuf-Fenhauer, S.6
Meitinger, T.7
Lipson, T.8
Goodship, J.9
Scrambler, P.10
-
7
-
-
0022967803
-
Construction of human chromosome-specific DNA libraries from flow-sorted chromosomes
-
Deaven LL, Van Dilla M, Barthold MF, Carrano A, Cram L, Fuscoe JC, Gray JW, Hildebrand CE, Moyzis RK, Perlman J: Construction of human chromosome-specific DNA libraries from flow-sorted chromosomes. Cold Spring Harb Symp quant Biol 51:159-167(1986).
-
(1986)
Cold Spring Harb Symp Quant Biol
, vol.51
, pp. 159-167
-
-
Deaven, L.V.1
Dilla, M.2
Barthold, M.F.3
Carranofuscoe, A.L.4
Gray, J.C.5
-
8
-
-
0027327852
-
Three human glutamate dehydrogenase genes (GLUDI, GLIJDP2 and GLUDP3) arc located on chromosome lOq. but are not closely physically linked
-
Deloukas P. Dauwcrsc JG. Moschonas NK, van Om-men G-JB, van Loon APGM: Three human glutamate dehydrogenase genes (GLUDI, GLIJDP2 and GLUDP3) arc located on chromosome lOq. but are not closely physically linked. Genomics 17:676-681 (1993).
-
(1993)
Genomics
, vol.17
, pp. 676-681
-
-
Deloukas, P.1
Dauwcrsc, J.G.2
Moschonas, N.K.3
Van Om-Men, G.-J.4
Van Loon, A.5
-
9
-
-
13344259999
-
A compehensive genetic map of the human genome based on 5,264 microsatcllites
-
Dib C. Fauré S. Fizames C. Samson D. Drouot N. Vignal A. Millasseau P. Marc S. Hazan J. Seboun E, Lathrop M, Gyapay G, Morissettc J. Weissenbach J: A compehensive genetic map of the human genome based on 5,264 microsatcllites. Nature 380:152-154(1996).
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Fauré, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
Marc, S.8
Hazan, J.9
Seboun, E.10
Lathrop, M.11
Gyapay, G.12
Morissettc, J.13
Weissenbach, J.14
-
10
-
-
0030896418
-
Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and Hirschsprung disease
-
Eng C. Mulligan LM: Mutations of the RET proto-oncogene in the multiple endocrine neoplasia type 2 syndromes, related sporadic tumours, and Hirschsprung disease. Hum Mutat 9:97-109 (1997).
-
(1997)
Hum Mutat
, vol.9
, pp. 97-109
-
-
Eng, C.1
Mulligan, L.M.2
-
11
-
-
0028214455
-
A radiation hybrid map of human chromosome 18
-
Francke U. Chang E, Comeau K. Geigle E-M. Giaca-lone J. Li X, Luna J. Moon A, Welch S, Wiigenbus P: A radiation hybrid map of human chromosome 18. Cytogenet Cel I Genet 66:196-213 (1994).
-
(1994)
Cytogenet Cel I Genet
, vol.66
, pp. 196-213
-
-
Francke, U.1
Chang, E.2
Comeau, K.3
Geigle, E.-M.4
Giaca-Lone, J.5
Li, X.6
Luna, J.7
Moon, A.8
Welch, S.9
Wiigenbus, P.10
-
12
-
-
0016862453
-
New method for mapping genes in human chromosomes
-
Goss SJ. Harris H: New method for mapping genes in human chromosomes. Nature 255:680-684 (1975).
-
(1975)
Nature
, vol.255
, pp. 680-684
-
-
Goss, S.J.1
Harris, H.2
-
13
-
-
9044240048
-
A radiation hybrid map of the human genome
-
Gyapay G. Schmitt K. Fizames C. Jones H. Vega-Czar-ny N, Spillett D. Muselet D, Prud'Homme JF, Dib C. Auffray C. Morissettc J. Weissenbach J. Good-fellow PN: A radiation hybrid map of the human genome. Hum molec Genet 5:339-346 (1996).
-
(1996)
Hum Molec Genet
, vol.5
, pp. 339-346
-
-
Gyapay, G.1
Schmitt, K.2
Fizames, C.3
Jones, H.4
Vega-Czar-Ny, N.5
Spillett, D.6
Muselet, D.7
Prud'homme, J.F.8
Dib, C.9
Auffray, C.10
Morissettc, J.11
Weissenbach, J.12
Good-Fellow, P.N.13
-
14
-
-
0029416826
-
An STS-bascd map of the human genome
-
Hudson TJ. Stein LD. Gerety SS. Ma J. Castle AB. Silva JS. Slonim DK. Baptista R. Kruglyak L, Xu Orlin JB. Birrcn BW. Goodman N. Weissenbach J. Hawkins TL, Foote S.: An STS-bascd map of the human genome. Science 270:1945-1954(1995).
-
(1995)
Science
, vol.270
, pp. 1945-1954
-
-
Hudson, T.J.1
Stein, L.D.2
Gerety, S.S.3
Ma, J.4
Castle, A.B.5
Silva, J.S.6
Slonim, D.K.7
Baptista, R.8
Kruglyak Xu, L.9
Orlin, J.B.10
Birrcn, B.W.11
Goodman, N.12
Weissenbach, J.13
Hawkins, T.L.14
Foote, S.15
-
15
-
-
0028318417
-
A new bacteriophage PI-derived vector for the propagation of large human DNA fragments
-
Ioaimou PA, Amemiya CT, Games J. Kroisel PM, Shi-zuya H. Chen C. Batzer MA, de Jong PJ: A new bacteriophage PI-derived vector for the propagation of large human DNA fragments. Nature Genet 6:84-89(1994).
-
(1994)
Nature Genet
, vol.6
, pp. 84-89
-
-
Ioaimou, P.A.1
Amemiya, C.T.2
Games, J.3
Kroisel, P.M.4
Shi-Zuya, H.5
Chen, C.6
Batzer, M.A.7
De Jong, P.J.8
-
16
-
-
0028113931
-
Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2
-
Jabs EW, Li X, Scolt AF, Meyers G, Chen C, Eccles M, Mao J, Chamas LR, Jackson CE, Jaye M: Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2. Nature Genet 8:275-279 (1994).
-
(1994)
Nature Genet
, vol.8
, pp. 275-279
-
-
Jabs, E.W.1
Li, X.2
Scolt, A.F.3
Meyers, G.4
Chen, C.5
Eccles, M.6
Mao, J.7
Chamas, L.R.8
Jackson, C.E.9
Jaye, M.10
-
17
-
-
0028709436
-
The EUROGF.M map of human chromosome 10
-
Kapsetaki M, Kokkinaki M, Angelicheva D, Lubyova B, Mavraki H, Argyrokastritis A, Vergnaud G,: The EUROGF.M map of human chromosome 10. Eur J hum Genet 2:222-223(1994).
-
(1994)
Eur J Hum Genet
, vol.2
, pp. 222-223
-
-
Kapsetaki, M.1
Kokkinaki, M.2
Angelicheva, D.3
Lubyova, B.4
Mavraki, H.5
Argyrokastritis, A.6
Vergnaud, G.7
-
18
-
-
0028982648
-
Eigenanalysis of DAPl-staincd chromosomes: Tools and strategies toward computer-assisted analysis of FISH experiments
-
Knapp RD. Smith LC. Baldini A: Eigenanalysis of DAPl-staincd chromosomes: tools and strategies toward computer-assisted analysis of FISH experiments. Cytogenet Cell Genet 69:81-86 (1995).
-
(1995)
Cytogenet Cell Genet
, vol.69
, pp. 81-86
-
-
Knapp, R.D.1
Smith, L.C.2
Baldini, A.3
-
19
-
-
0023946286
-
Human genome organisation: Alu. Lines and the molecular structure of mctaphase chromosome bands
-
Korenberg JR. Rvkowski MC: Human genome organisation: Alu. Lines and the molecular structure of mctaphase chromosome bands. Cell 53:391-400 (1988).
-
(1988)
Cell
, vol.53
, pp. 391-400
-
-
Korenberg, J.R.1
Rvkowski, M.C.2
-
20
-
-
0027502802
-
Dual Alu polymerase chain reaction primers and conditions lor isolation of human chromosome painting probes from hybrid cells
-
Liu P, Siciliano S, Seong D, Craig J, Zhao Z, de Jong PJ, Siciliano MJ: Dual Alu polymerase chain reaction primers and conditions lor isolation of human chromosome painting probes from hybrid cells. Cancer Genet Cytogenet 65:93-99(1993).
-
(1993)
Cancer Genet Cytogenet
, vol.65
, pp. 93-99
-
-
Liu, P.1
Siciliano, S.2
Seong, D.3
Craig, J.4
Zhao, Z.5
De Jong, P.J.6
Siciliano, M.J.7
-
22
-
-
0031299557
-
Report of the second international workshop on human chromosome 10 mapping 1997
-
Meitinger T. Scharfe C. Call K. Moschonas N: Report of the second international workshop on human chromosome 10 mapping 1997. Cytogenet Cell Genet 78:183-196 (1997).
-
(1997)
Cytogenet Cell Genet
, vol.78
, pp. 183-196
-
-
Meitinger, T.1
Scharfe, C.2
Call, K.3
Moschonas, N.4
-
23
-
-
0029877186
-
Report of the first international workshop on human chromosome 10 mapping 1995
-
Moschonas NK. Spurr NK. Mao J: Report of the first international workshop on human chromosome 10 mapping 1995. Cytogenet Cell Genet 72:99-112 (1996).
-
(1996)
Cytogenet Cell Genet
, vol.72
, pp. 99-112
-
-
Moschonas, N.K.1
Spurr, N.K.2
Mao, J.3
-
24
-
-
0030025687
-
Comparative fluorescence in situ hybridization mapping of primate chromosomes with .Iht-PCR generated probes from human/rodent somatic cell hybrids
-
Muller S, Koehler U. Wienbcrg J. Marzclla R. Finelli P. Antonacci R. Rocchi M. Archidiácono N: Comparative fluorescence in situ hybridization mapping of primate chromosomes with .Iht-PCR generated probes from human/rodent somatic cell hybrids. Chront Res 4:38-42 (1996).
-
(1996)
Chront Res
, vol.4
, pp. 38-42
-
-
Muller, S.1
Koehler, U.2
Wienbcrg, J.3
Marzclla, R.4
Finelli, P.5
Antonaccirocchi, R.6
Archidiácono, M.N.7
-
25
-
-
0030992653
-
Identification of a 790-kilobase region of common allelic loss in chromosome 10q25-q26 in human endometrial cancer
-
Nagase S. Yantakawa H. Salo S. Yajima A. Horii A: Identification of a 790-kilobase region of common allelic loss in chromosome 10q25-q26 in human endometrial cancer. Cancer Res 57:1630-1633 (1997).
-
(1997)
Cancer Res
, vol.57
, pp. 1630-1633
-
-
Nagase, S.1
Yantakawa, H.2
Salo, S.3
Yajima, A.4
Horii, A.5
-
26
-
-
1542471167
-
Alu-polymerasc chain reaction: A method for rapid isolation of human-specific sequences from complex DNA sources
-
USA
-
Nelson DL. Ledbetter SA. Corbo L. Victoria MF. Ram-irez-Solis R. Webster TD. Ledbetter DH. Caskey CT: Alu-polymerasc chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sources. Proc nail Acad Sci, USA 86:6686-6690(1989).
-
(1989)
Proc Nail Acad Sci
, vol.86
, pp. 6686-6690
-
-
Nelson, D.L.1
Ledbetter, S.A.2
Corbo, L.3
Victoria, M.F.4
Ram-Irez-Solis, R.5
Webster, T.D.6
Ledbetter, D.H.7
Caskey, C.T.8
-
27
-
-
0031568287
-
Toward cloning of a novel ataxia gene: Refined assignment and physical map of the lOSC'A locus (SCA8) on I0q24
-
Nikali K. Isosomppi J. Lonnqvist T. Mao JL, Suomal-ainen A. Pellonen L: Toward cloning of a novel ataxia gene: refined assignment and physical map of the lOSC'A locus (SCA8) on I0q24. Genomics 39:185-191 (1997).
-
(1997)
Genomics
, vol.39
, pp. 185-191
-
-
Nikali, K.1
Isosomppi, J.2
Lonnqvist, T.3
Mao, J.L.4
-
29
-
-
15844388219
-
Fibroblast growth factor receptor 2 mutations in Beare-Stcv-enson cutis gyrata syndrome
-
Przvlepa KA, Paznckas W. Zhang M. Golabi M. Bias w. Bamshad MJ. Carey JC. Hall BD. Fibroblast growth factor receptor 2 mutations in Beare-Stcv-enson cutis gyrata syndrome. Nature Genet 13:492-494 (1996).
-
(1996)
Nature Genet
, vol.13
, pp. 492-494
-
-
Przvlepa, K.A.1
Paznckas, W.2
Zhang, M.3
Golabi, M.B.W.4
Bamshad, M.J.5
Carey, J.C.6
Hall, B.D.7
-
31
-
-
0029109137
-
Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes
-
Rutland P. Pulleyn I J. Reardon W, Baraitser M. Hayward R. Jones B. Malcolm S, Winter RM. Oldridge M, Slaney SF. Poole MD. Wilkie AOM: Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes. Nature Genet 9:173-176(1995).
-
(1995)
Nature Genet
, vol.9
, pp. 173-176
-
-
Rutland, P.1
Pulleyn, I.J.2
Reardon, W.3
Baraitser, M.4
Hayward, R.5
Jones, B.6
Malcolm, S.7
Winter, R.M.8
Oldridge, M.9
Slaney, S.F.10
Poole, M.D.11
Wilkie, A.12
-
32
-
-
0028069099
-
European Gene Mapping Project (EUROGEM): Genetic maps based on the CEPH reference families
-
Spurr NK. Bryant SP. Attwood J. Nvberg K. Cox SA. Mills A, Bains R. Warne D, Cullin L. Povey S. Sebaoun JM. Weissenbach J. European Gene Mapping Project (EUROGEM): genetic maps based on the CEPH reference families. Eur J hum Genet 2:193-252 (1994).
-
(1994)
Eur J Hum Genet
, vol.2
, pp. 193-252
-
-
Spurr, N.K.1
Bryant, S.P.2
Attwood, J.3
Nvberg, K.4
Cox, S.A.5
Mills, A.6
Bains, R.7
Warne, D.8
Cullin, L.9
Povey, S.10
Sebaoun, J.M.11
Weissenbach, J.12
-
33
-
-
0027290695
-
Structure and expression analysis of a novel member of the human glutamate dehydrogenase (GLUD) gene family mapped to chromosome 1 Op 11.2
-
Tzimagiotgis G, Leversha M. 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 1 Op 11.2. Hum Genet 91:433-438 (1993).
-
(1993)
Hum Genet
, vol.91
, pp. 433-438
-
-
Tzimagiotgis, G.1
Leversha, M.2
Chroniary, K.3
Goulielmos, G.4
Sargent, C.A.5
Ferguson-Smith, M.6
Moschonas, N.K.7
-
34
-
-
0028798546
-
Apcrt syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome
-
Wilkie AOM. Slaney SF. Oldridge M. Poole MD. Ashworth GJ. Hockley AD. Hayward RD. David DJ. Pulleyn LL Rutland P. Malcolm S, Winter RM, Reardon W: Apcrt syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome. Nature Genet 9:165-172 (1995).
-
(1995)
Nature Genet
, vol.9
, pp. 165-172
-
-
Wilkie, A.1
Slaney, S.F.2
Oldridge, M.3
Poole, M.D.4
Ashworth, G.J.5
Hockley, A.D.6
Hayward, R.D.7
David, D.J.8
Pulleyn Ll Rutland, P.9
Malcolm, S.10
Winter, R.M.11
Reardon, W.12
-
35
-
-
0020027910
-
The origin of man: A chromosomal pictorial legacy
-
Yunis JJ. Prakash O: The origin of man: a chromosomal pictorial legacy. Science 215:1525- 1530 (1982)
-
(1982)
Science
, vol.215
-
-
Yunis, J.J.1
Prakash, O.2
|