-
1
-
-
0028942620
-
A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3 and PHKA2 genes
-
Alitalo T, Francis F, Kere J, Lehrach H, Schlessinger D, Willard HF (1995) A 6-Mb YAC contig in Xp22.1-p22.2 spanning the DXS69E, XE59, GLRA2, PIGA, GRPR, CALB3 and PHKA2 genes. Genomics 25, 691-700
-
(1995)
Genomics
, vol.25
, pp. 691-700
-
-
Alitalo, T.1
Francis, F.2
Kere, J.3
Lehrach, H.4
Schlessinger, D.5
Willard, H.F.6
-
2
-
-
0028304893
-
Nance-Horan syndrome: Linkage analysis in a family from the Netherlands
-
Bergen AA, Ten Brink J, Schuurman EJ, Bleeker-Wagemakers EM (1994) Nance-Horan syndrome: linkage analysis in a family from the Netherlands. Genomics 21, 238-240
-
(1994)
Genomics
, vol.21
, pp. 238-240
-
-
Bergen, A.A.1
Ten Brink, J.2
Schuurman, E.J.3
Bleeker-Wagemakers, E.M.4
-
3
-
-
0028821829
-
Crossover analysis in a British family suggests that Coffin-Lowry syndrome maps to a 3.4-cM interval in Xp22
-
Bird H, Collins AL, Oley C, Lindsay S (1995) Crossover analysis in a British family suggests that Coffin-Lowry syndrome maps to a 3.4-cM interval in Xp22. Am J Med Genet 59, 512-516
-
(1995)
Am J Med Genet
, vol.59
, pp. 512-516
-
-
Bird, H.1
Collins, A.L.2
Oley, C.3
Lindsay, S.4
-
4
-
-
0026878925
-
Dinucleotide repeat polymorphisms at the DXS365, DXS443 and DXS451 loci
-
Browne D, Barker D, Litt M. (1992) Dinucleotide repeat polymorphisms at the DXS365, DXS443 and DXS451 loci. Hum Mol Genet 1, 213
-
(1992)
Hum Mol Genet
, vol.1
, pp. 213
-
-
Browne, D.1
Barker, D.2
Litt, M.3
-
5
-
-
0029653653
-
A YAC contig map of the human genome
-
Chumakov IM, Rigault P, Le Gall I, Bellanné-Chantelot C, Billault A, Guillou S, Soularue P, Guasconi G, Poullier E, Gros I, Belova M, Sambucy JL, Susini L, Gervy P, Glibert F, Beaufils S, Bui H, Massart C, De Tand MF, Dukasz F, Lecoulant S, Ougen P, Perrot V, Saumler M, (1995) A YAC contig map of the human genome. Nature 377 Suppl, 175-183
-
(1995)
Nature
, vol.377
, Issue.SUPPL.
, pp. 175-183
-
-
Chumakov, I.M.1
Rigault, P.2
Le Gall, I.3
Bellanné-Chantelot, C.4
Billault, A.5
Guillou, S.6
Soularue, P.7
Guasconi, G.8
Poullier, E.9
Gros, I.10
Belova, M.11
Sambucy, J.L.12
Susini, L.13
Gervy, P.14
Glibert, F.15
Beaufils, S.16
Bui, H.17
Massart, C.18
De Tand, M.F.19
Dukasz, F.20
Lecoulant, S.21
Ougen, P.22
Perrot, V.23
Saumler, M.24
more..
-
6
-
-
0027723477
-
A first generation physical map of the human genome
-
Cohen D, Chumakov I, Weissenbach J. (1993) A first generation physical map of the human genome. Nature 366, 698-701
-
(1993)
Nature
, vol.366
, pp. 698-701
-
-
Cohen, D.1
Chumakov, I.2
Weissenbach, J.3
-
7
-
-
19244364120
-
Closing in on the Rieger syndrome gene on 4q25: Mapping translocation breakpoints within a 50-kb region
-
Datson NA, Semina E, Van Staalduinen AAA, Dauwerse HG, Meershoek EJ, Heus JJ, Frants RR, Den Dunnen JT, Murray JC, Van Ommen GJB (1996a) Closing in on the Rieger syndrome gene on 4q25: mapping translocation breakpoints within a 50-kb region. Am J Hum Genet 59, 1297-1305
-
(1996)
Am J Hum Genet
, vol.59
, pp. 1297-1305
-
-
Datson, N.A.1
Semina, E.2
Van Staalduinen, A.A.A.3
Dauwerse, H.G.4
Meershoek, E.J.5
Heus, J.J.6
Frants, R.R.7
Den Dunnen, J.T.8
Murray, J.C.9
Van Ommen, G.J.B.10
-
8
-
-
0029914506
-
Scanning for genes in large genomic regions: Cosmid-based exon trapping of multiple exons in a single product
-
Datson NA, Van de Vosse E, Dauwerse HG, Bout M, Van Ommen GJB, Den Dunnen JT (1996b) Scanning for genes in large genomic regions: cosmid-based exon trapping of multiple exons in a single product. Nucleic Acids Res. 24, 1105-1111
-
(1996)
Nucleic Acids Res.
, vol.24
, pp. 1105-1111
-
-
Datson, N.A.1
Van De Vosse, E.2
Dauwerse, H.G.3
Bout, M.4
Van Ommen, G.J.B.5
Den Dunnen, J.T.6
-
9
-
-
0019868389
-
Base sequence studies of 300 nucleotide renatured repeated human DNA clones
-
Deininger PL, Jolly DJ, Rubin CM, Friedmann T, Schmid CW (1993) Base sequence studies of 300 nucleotide renatured repeated human DNA clones. J Mol Biol 151, 17-33
-
(1993)
J Mol Biol
, vol.151
, pp. 17-33
-
-
Deininger, P.L.1
Jolly, D.J.2
Rubin, C.M.3
Friedmann, T.4
Schmid, C.W.5
-
11
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5,264 microsatellites
-
Dib C, Faure S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P, Marc S, Hazan J, Seboun E, Gyapay G, Morissette J, Weissenbach J (1996) A comprehensive genetic map of the human genome based on 5,264 microsatellites. Nature 380, 152-154
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, 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
Gyapay, G.11
Morissette, J.12
Weissenbach, J.13
-
12
-
-
0028892091
-
An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3
-
Ferrero GB, Franco B, Roth EJ, Firulli BA, Borsani G, Delmas-Mata J, Weissenbach J, Halley G, Schlessinger D, Chinault AC, Zoghbi HY, Nelson DL, Ballabio A (1995) An integrated physical and genetic map of a 35 Mb region on chromosome Xp22.3-Xp21.3. Hum Mol Genet 4, 1821-1827
-
(1995)
Hum Mol Genet
, vol.4
, pp. 1821-1827
-
-
Ferrero, G.B.1
Franco, B.2
Roth, E.J.3
Firulli, B.A.4
Borsani, G.5
Delmas-Mata, J.6
Weissenbach, J.7
Halley, G.8
Schlessinger, D.9
Chinault, A.C.10
Zoghbi, H.Y.11
Nelson, D.L.12
Ballabio, A.13
-
13
-
-
9044240048
-
A radiation hybrid map of the human genome
-
Gyapay G, Schmitt K, Fizames C. Jones H, Vega-Czarny N, Spillett D, Muselet D, Prud'Homme J-F, Dib C, Auffray C, Morisette J, Weissenbach J, Goodfellow P (1996) A radiation hybrid map of the human genome. Hum Mol Genet 5, 339-346
-
(1996)
Hum Mol Genet
, vol.5
, pp. 339-346
-
-
Gyapay, G.1
Schmitt, K.2
Fizames, C.3
Jones, H.4
Vega-Czarny, N.5
Spillett, D.6
Muselet, D.7
Prud'Homme, J.-F.8
Dib, C.9
Auffray, C.10
Morisette, J.11
Weissenbach, J.12
Goodfellow, P.13
-
15
-
-
0030955038
-
Linkage disequilibrium and physical mapping of X-linked juvenile retinoschisis
-
in press
-
Huopaniemi L, Rantala A, Tahvanainen E, De la Chapelle A, Alitalo T (1997) Linkage disequilibrium and physical mapping of X-linked juvenile retinoschisis. Am J Hum Genet, in press.
-
(1997)
Am J Hum Genet
-
-
Huopaniemi, L.1
Rantala, A.2
Tahvanainen, E.3
De La Chapelle, A.4
Alitalo, T.5
-
16
-
-
0026440240
-
Mapping human chromosomes by walking with Sequence-Tagged Sites from end fragments of Yeast Artificial Chromosome inserts
-
Kere J, Nagaraja R, Mumm S, Ciccodicola A, D'Urso M, Schlessinger D (1992) Mapping human chromosomes by walking with Sequence-Tagged Sites from end fragments of Yeast Artificial Chromosome inserts. Genomics 14, 241-248
-
(1992)
Genomics
, vol.14
, pp. 241-248
-
-
Kere, J.1
Nagaraja, R.2
Mumm, S.3
Ciccodicola, A.4
D'Urso, M.5
Schlessinger, D.6
-
18
-
-
0029076161
-
Refinement of the localisation of X-linked keratosis follicularis spinulosa decalvans (KFSD) gene in Xp22.1-p22.2
-
Oosterwijk JC, Van der Wielen MJR, Van de Vosse E, Voorhoeve E, Bakker E (1995) Refinement of the localisation of X-linked keratosis follicularis spinulosa decalvans (KFSD) gene in Xp22.1-p22.2. J Med Genet 32, 736-739
-
(1995)
J Med Genet
, vol.32
, pp. 736-739
-
-
Oosterwijk, J.C.1
Van Der Wielen, M.J.R.2
Van De Vosse, E.3
Voorhoeve, E.4
Bakker, E.5
-
19
-
-
0025037630
-
Generation of deletion derivatives by targeted transformation of human-derived yeast artificial chromosomes
-
Pavan WJ, Hieter P, Reeves RH (1990) Generation of deletion derivatives by targeted transformation of human-derived yeast artificial chromosomes. Proc Natl Acad Sci USA. 87, 1300-1304
-
(1990)
Proc Natl Acad Sci USA.
, vol.87
, pp. 1300-1304
-
-
Pavan, W.J.1
Hieter, P.2
Reeves, R.H.3
-
20
-
-
0029678618
-
Use of YAC fragmentation to delimit a duplicated region on human chromosome 21
-
Potier M-C, Dutriaux A, Reeves R (1996) Use of YAC fragmentation to delimit a duplicated region on human chromosome 21. Mamm Genome 7, 85-88
-
(1996)
Mamm Genome
, vol.7
, pp. 85-88
-
-
Potier, M.-C.1
Dutriaux, A.2
Reeves, R.3
-
21
-
-
0344570067
-
Construction, characterization and screening of YAC libraries
-
R. Anand, ed. (London: Academic Press)
-
Riley JH, Ogilvie D, Anand R (1992) Construction, characterization and screening of YAC libraries. In: Techniques for the Analysis of Complex Genomes, R. Anand, ed. (London: Academic Press) pp 59-79
-
(1992)
Techniques for the Analysis of Complex Genomes
, pp. 59-79
-
-
Riley, J.H.1
Ogilvie, D.2
Anand, R.3
-
22
-
-
0027291742
-
A high resolution deletion map of human chromosome Xp22
-
Schaefer L, Ferrero GB Grillo A, Bassi MT, Roth EJ, Wapenaar MC, Van Ommen GJB, Mohandas TK, Rocchi M, Zoghbi HY, Ballabio A (1993) A high resolution deletion map of human chromosome Xp22. Nature Genet 4, 272-279
-
(1993)
Nature Genet
, vol.4
, pp. 272-279
-
-
Schaefer, L.1
Ferrero, G.B.2
Grillo, A.3
Bassi, M.T.4
Roth, E.J.5
Wapenaar, M.C.6
Van Ommen, G.J.B.7
Mohandas, T.K.8
Rocchi, M.9
Zoghbi, H.Y.10
Ballabio, A.11
-
23
-
-
0028065054
-
Yeast karl mutants provide an effective method for YAC transfer to new hosts
-
Spencer F, Hugerat Y, Simchen G, Hurko O, Connelly C, Hieter P (1994) Yeast karl mutants provide an effective method for YAC transfer to new hosts. Genomics 22, 118-126
-
(1994)
Genomics
, vol.22
, pp. 118-126
-
-
Spencer, F.1
Hugerat, Y.2
Simchen, G.3
Hurko, O.4
Connelly, C.5
Hieter, P.6
-
24
-
-
13344275870
-
Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1
-
Trump D, Pilia G, Dixon PH, Wooding C, Thakrar R, Leigh SEA, Nagaraja R, Whyte MP, Schlessinger D, Thakker RV (1996) Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1 Hum Genet 97, 60-68
-
(1996)
Hum Genet
, vol.97
, pp. 60-68
-
-
Trump, D.1
Pilia, G.2
Dixon, P.H.3
Wooding, C.4
Thakrar, R.5
Leigh, S.E.A.6
Nagaraja, R.7
Whyte, M.P.8
Schlessinger, D.9
Thakker, R.V.10
-
25
-
-
0027749355
-
A CA-repeat polymorphism near DXS418 (P122)
-
Van de Vosse E, Booms PFM, Vossen RHAM, Wapenaar MC, Van Ommen GJB, Den Dunnen JT (1993) A CA-repeat polymorphism near DXS418 (P122). Hum Mol Genet 2, 1202
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1202
-
-
Van De Vosse, E.1
Booms, P.F.M.2
Vossen, R.H.A.M.3
Wapenaar, M.C.4
Van Ommen, G.J.B.5
Den Dunnen, J.T.6
-
26
-
-
0029918833
-
A Xp22.1-p22.2 YAC contig encompassing the disease loci for RS, KFSD, CLS, HYP and RP15; refined localization of RS
-
Van de Vosse E, Bergen AAB, Meershoek EJ, Oosterwijk JC, Gregory S, Bakker B, Weissenbach J, Coffey AJ, Van Ommen GJB, Den Dunnen JT (1996) A Xp22.1-p22.2 YAC contig encompassing the disease loci for RS, KFSD, CLS, HYP and RP15; refined localization of RS. Eur J Hum Genet 4, 101-104
-
(1996)
Eur J Hum Genet
, vol.4
, pp. 101-104
-
-
Van De Vosse, E.1
Bergen, A.A.B.2
Meershoek, E.J.3
Oosterwijk, J.C.4
Gregory, S.5
Bakker, B.6
Weissenbach, J.7
Coffey, A.J.8
Van Ommen, G.J.B.9
Den Dunnen, J.T.10
|