-
1
-
-
0026089211
-
Localization of the Åland Island eye disease locus to the pericentromeric region of the X chromosome by linkage analysis
-
Alitalo, T., Kruse, T. A., Forsius, H., Eriksson, A. W., and de la Chapelle, A. (1991). Localization of the Åland Island Eye Disease locus to the pericentromeric region of the X chromosome by linkage analysis. Am. J. Hum. Genet. 48: 31-38.
-
(1991)
Am. J. Hum. Genet.
, vol.48
, pp. 31-38
-
-
Alitalo, T.1
Kruse, T.A.2
Forsius, H.3
Eriksson, A.W.4
De La Chapelle, A.5
-
2
-
-
0025183708
-
Basic local alignment search tool
-
Altschul, S. F., Gish, W., Miller, W., Myers, E. W., and Lipman, D. J. (1990). Basic local alignment search tool. J. Mol. Biol. 215: 403-410.
-
(1990)
J. Mol. Biol.
, vol.215
, pp. 403-410
-
-
Altschul, S.F.1
Gish, W.2
Miller, W.3
Myers, E.W.4
Lipman, D.J.5
-
3
-
-
0027474273
-
Manifestations of X-linked congenital stationary night blindness in three daughters of an affected male: Demonstration of homozygosity
-
Bech-Hansen, N. T., and Pearce, W. G. (1993). Manifestations of X-linked Congenital Stationary Night Blindness in three daughters of an affected male: Demonstration of homozygosity. Am. J. Hum. Genet. 52: 71-77.
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 71-77
-
-
Bech-Hansen, N.T.1
Pearce, W.G.2
-
4
-
-
0025061096
-
TFE3: A helixloop-helix protein that activates transcription through the immunoglobulin enhancer μE3 motif
-
Beckmann, H., Su, L.-K., and Kadesch, T. (1990). TFE3: A helixloop-helix protein that activates transcription through the immunoglobulin enhancer μE3 motif. Genes Dev. 4: 167-179.
-
(1990)
Genes Dev.
, vol.4
, pp. 167-179
-
-
Beckmann, H.1
Su, L.-K.2
Kadesch, T.3
-
5
-
-
0025963263
-
Mapping the gene encoding the human erythroid transcription factor NFE1-GF1 to Xp11.23
-
Caiulo, A., Nicolis, S., Bianchi, P., Zuffardi, O., Bardoni, B., Maraschio, P., Ottolenghi, S., Camerino, G., and Giglioni, B. (1991). Mapping the gene encoding the human erythroid transcription factor NFE1-GF1 to Xp11.23. Hum. Genet. 86: 388-390.
-
(1991)
Hum. Genet.
, vol.86
, pp. 388-390
-
-
Caiulo, A.1
Nicolis, S.2
Bianchi, P.3
Zuffardi, O.4
Bardoni, B.5
Maraschio, P.6
Ottolenghi, S.7
Camerino, G.8
Giglioni, B.9
-
6
-
-
0027723477
-
A first-generation physical map of the human genome
-
Cohen, D., Chumakov, I., and 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
-
-
0028236066
-
A 1.8-Mb YAC contig in Xp11.23: Identification of CpG islands and physical mapping of CA repeats in a region of high gene density
-
Coleman, M. P., Nemeth, A. H., Campbell, L., Raut, C. P., Weissenbach, J., and Davies, K. E. (1994). A 1.8-Mb YAC contig in Xp11.23: Identification of CpG islands and physical mapping of CA repeats in a region of high gene density. Genomics 21: 337-343.
-
(1994)
Genomics
, vol.21
, pp. 337-343
-
-
Coleman, M.P.1
Nemeth, A.H.2
Campbell, L.3
Raut, C.P.4
Weissenbach, J.5
Davies, K.E.6
-
8
-
-
0027280576
-
Sublocalization of the synovial sarcoma-associated t(X; 18) chromosomal breakpoint in Xp11.2 using cosmid cloning and fluorescence in situ hybridization
-
de Leeuw, B., Suijkerbuijk, R. F., Balemans, M., Sinke, R. J., de Jong, B., Molenaar, W. M., Meloni, A. M., Sandberg, A. A., Geraghty, M., Hofker, M., Ropers, H. H., and van Kessel, A. G. (1993). Sublocalization of the synovial sarcoma-associated t(X; 18) chromosomal breakpoint in Xp11.2 using cosmid cloning and fluorescence in situ hybridization. Oncogene 8: 1457-1463.
-
(1993)
Oncogene
, vol.8
, pp. 1457-1463
-
-
De Leeuw, B.1
Suijkerbuijk, R.F.2
Balemans, M.3
Sinke, R.J.4
De Jong, B.5
Molenaar, W.M.6
Meloni, A.M.7
Sandberg, A.A.8
Geraghty, M.9
Hofker, M.10
Ropers, H.H.11
Van Kessel, A.G.12
-
9
-
-
0027937223
-
Isolation of a novel gene mutated in Wiskott-Aldrich syndrome
-
Derry, J. M. J., Ochs, H. D., and Francke, U. (1994). Isolation of a novel gene mutated in Wiskott-Aldrich syndrome. Cell 78: 635-644.
-
(1994)
Cell
, vol.78
, pp. 635-644
-
-
Derry, J.M.J.1
Ochs, H.D.2
Francke, U.3
-
10
-
-
0028264926
-
A linkage map of microsatellite markers on the human X chromosome
-
Donnelly, A., Kozman, H., Gedeon, A. K., Webb, S., Lynch, M., Sutherland, G. R., Richards, R. I., and Mulley, J. C. (1994). A linkage map of microsatellite markers on the human X chromosome. Genomics 20: 363-370.
-
(1994)
Genomics
, vol.20
, pp. 363-370
-
-
Donnelly, A.1
Kozman, H.2
Gedeon, A.K.3
Webb, S.4
Lynch, M.5
Sutherland, G.R.6
Richards, R.I.7
Mulley, J.C.8
-
11
-
-
0024691032
-
Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22
-
Fraser, N. J., Boyd, Y., and Craig, I. (1989). Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22. Genomics 5: 144-148.
-
(1989)
Genomics
, vol.5
, pp. 144-148
-
-
Fraser, N.J.1
Boyd, Y.2
Craig, I.3
-
12
-
-
0027310955
-
The isolation of cDNAs from OATL1 at Xp11.2 using a 480-kb YAC
-
Geraghty, M. T., Brody, L. C., Martin, L. S., Marble, M., Kearns, W., Pearson, P., Monaco, A. P., Lehrach, H., and Valle, D. (1993). The isolation of cDNAs from OATL1 at Xp11.2 using a 480-kb YAC. Genomics 16: 440-446.
-
(1993)
Genomics
, vol.16
, pp. 440-446
-
-
Geraghty, M.T.1
Brody, L.C.2
Martin, L.S.3
Marble, M.4
Kearns, W.5
Pearson, P.6
Monaco, A.P.7
Lehrach, H.8
Valle, D.9
-
13
-
-
0025346105
-
Sublocalisation of the X breakpoint in the translocation (X; 18)(p11.2;q11.2) primary change in synovial sarcomas
-
Gilgenkrantz, S., Chery, M., Teboul, M., Mujica, P., Leotard, B., Gregoire, M. J., Boman, F., Duprez, A., and Hanauer, A. (1990). Sublocalisation of the X breakpoint in the translocation (X; 18)(p11.2;q11.2) primary change in synovial sarcomas. Oncogene 5: 1063-1066.
-
(1990)
Oncogene
, vol.5
, pp. 1063-1066
-
-
Gilgenkrantz, S.1
Chery, M.2
Teboul, M.3
Mujica, P.4
Leotard, B.5
Gregoire, M.J.6
Boman, F.7
Duprez, A.8
Hanauer, A.9
-
14
-
-
0027482799
-
Genetic mapping of a cone and rod dysfunction (Åland Island eye disease) to the proximal short arm of the human X chromosome
-
Glass, I. A., Good, P., Coleman, M. P., Fullwood, P., Giles, M. G., Lindsay, S., Nemeth, A. H., Davies, K E., Willshaw, H. A., Fielder, A., Kilpatrick, M., and Farndon, P. A. (1993). Genetic mapping of a cone and rod dysfunction (Åland Island eye disease) to the proximal short arm of the human X chromosome. J. Med. Genet. 30: 1044-1050.
-
(1993)
J. Med. Genet.
, vol.30
, pp. 1044-1050
-
-
Glass, I.A.1
Good, P.2
Coleman, M.P.3
Fullwood, P.4
Giles, M.G.5
Lindsay, S.6
Nemeth, A.H.7
Davies, K.E.8
Willshaw, H.A.9
Fielder, A.10
Kilpatrick, M.11
Farndon, P.A.12
-
15
-
-
0026254597
-
Sequence-tagged site (STS) content mapping of human chromosomes: Theoretical considerations and early experiences
-
Green, E. D., and Green, P. (1991). Sequence-tagged site (STS) content mapping of human chromosomes: Theoretical considerations and early experiences. PCR Methods Appl. 1: 77-90.
-
(1991)
PCR Methods Appl.
, vol.1
, pp. 77-90
-
-
Green, E.D.1
Green, P.2
-
16
-
-
0028231090
-
The 1993-1994 Généthon human genetic linkage map
-
Gyapay, G., Morissette, J., Vignal, A., Dib, C., Fizames, C., Missasseau, P., Marc, S., Bernardi, G., Lathrop, M., and Weissenbach, J. (1994). The 1993-1994 Généthon human genetic linkage map. Nature Genet. 7: 246-339.
-
(1994)
Nature Genet.
, vol.7
, pp. 246-339
-
-
Gyapay, G.1
Morissette, J.2
Vignal, A.3
Dib, C.4
Fizames, C.5
Missasseau, P.6
Marc, S.7
Bernardi, G.8
Lathrop, M.9
Weissenbach, J.10
-
17
-
-
0028304894
-
Physical mapping in a YAC contig of 11 markers on the human X chromosome in Xp11.23
-
Hagemann, T., Surosky, R., Monaco, A. P., Lehrach, H., Rosen, F. S., and Kwan, S.-P. (1994). Physical mapping in a YAC contig of 11 markers on the human X chromosome in Xp11.23. Genomics 21: 262-265.
-
(1994)
Genomics
, vol.21
, pp. 262-265
-
-
Hagemann, T.1
Surosky, R.2
Monaco, A.P.3
Lehrach, H.4
Rosen, F.S.5
Kwan, S.-P.6
-
18
-
-
0028606172
-
Large human YACs constructed in a rad52 strain show a reduced rate of chimerism
-
Haldi, M., Perrot, V., Saumier, M., Desai, T., Cohen, D., Cherif, D., Ward, D., and Lander, E. S. (1994). Large human YACs constructed in a rad52 strain show a reduced rate of chimerism. Genomics 24: 478-484.
-
(1994)
Genomics
, vol.24
, pp. 478-484
-
-
Haldi, M.1
Perrot, V.2
Saumier, M.3
Desai, T.4
Cohen, D.5
Cherif, D.6
Ward, D.7
Lander, E.S.8
-
19
-
-
0025760204
-
Twenty-seven nonoverlapping zinc finger cDNAs from human T cells map to nine different chromosomes with apparent clustering
-
Huebner, K., Druck, T., Croce, C.M., and Thiesen, H.-J. (1991). Twenty-seven nonoverlapping zinc finger cDNAs from human T cells map to nine different chromosomes with apparent clustering. Am J. Hum Genet. 48: 726-740.
-
(1991)
Am J. Hum Genet.
, vol.48
, pp. 726-740
-
-
Huebner, K.1
Druck, T.2
Croce, C.M.3
Thiesen, H.-J.4
-
20
-
-
0021816507
-
Mapping DNA sequences in a human X chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation
-
Ingle, C., Williamson, R., de la Chapelle, A., Herva, R. R., Haapala, K., Bates, G., Willard, H. F., Pearson, P., and Davies, K. E. (1985). Mapping DNA sequences in a human X chromosome deletion which extends across the region of the Duchenne muscular dystrophy mutation. Am. J. Hum. Genet. 37: 451-462.
-
(1985)
Am. J. Hum. Genet.
, vol.37
, pp. 451-462
-
-
Ingle, C.1
Williamson, R.2
De La Chapelle, A.3
Herva, R.R.4
Haapala, K.5
Bates, G.6
Willard, H.F.7
Pearson, P.8
Davies, K.E.9
-
21
-
-
0028318417
-
A new bacteriophage P1-derived vector for the propagation of large human DNA fragments
-
Ioannou, P. A., Amemiya, C. T., Garnes, J., Kroisel, P. M., Shizuya, H., Chen, C., Batzer, M. A., and de Jong, P. J. (1994). A new bacteriophage P1-derived vector for the propagation of large human DNA fragments. Nature Genet. 6: 84-89.
-
(1994)
Nature Genet.
, vol.6
, pp. 84-89
-
-
Ioannou, P.A.1
Amemiya, C.T.2
Garnes, J.3
Kroisel, P.M.4
Shizuya, H.5
Chen, C.6
Batzer, M.A.7
De Jong, P.J.8
-
22
-
-
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., and 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
-
23
-
-
0028183128
-
Clustered organization of Kruppel zinc-finger genes at Xp11.23, flanking a translocation breakpoint at OATL1: A physical map with locus assignments for ZNF21, ZNF41, ZNF81, and ELK1
-
Knight, J. C., Grimaldi, G., Thiesen, H.-J., Bech-Hansen, N. T., Fletcher, C. D. M., and Coleman, M. P. (1994). Clustered organization of Kruppel Zinc-Finger genes at Xp11.23, flanking a translocation breakpoint at OATL1: A physical map with locus assignments for ZNF21, ZNF41, ZNF81, and ELK1. Genomics 21: 180-187.
-
(1994)
Genomics
, vol.21
, pp. 180-187
-
-
Knight, J.C.1
Grimaldi, G.2
Thiesen, H.-J.3
Bech-Hansen, N.T.4
Fletcher, C.D.M.5
Coleman, M.P.6
-
24
-
-
0028679188
-
Stability of YACs containing ribosomal or RCP/GCP locus DNA in wild-type S. cerevisiae and RAD mutant strains
-
Kohno, K., Wada, M., Schlessinger, D., D'Urso, M., Tanabe, S., Oshiro, T., and Imamoto, F. (1994). Stability of YACs containing ribosomal or RCP/GCP locus DNA in wild-type S. cerevisiae and RAD mutant strains. DNA Res. 1: 191-199.
-
(1994)
DNA Res.
, vol.1
, pp. 191-199
-
-
Kohno, K.1
Wada, M.2
Schlessinger, D.3
D'Urso, M.4
Tanabe, S.5
Oshiro, T.6
Imamoto, F.7
-
25
-
-
0029144041
-
A high-resolution map of genes, microsatellite markers, and new dinucleotide repeats from UBE1 to the GATA locus in the region Xp11.23
-
Kwan, S.-P., Hagemann, T. L., Blaese, R. M., and Rosen, F. S. (1995). A high-resolution map of genes, microsatellite markers, and new dinucleotide repeats from UBE1 to the GATA locus in the region Xp11.23. Genomics 29: 247-252.
-
(1995)
Genomics
, vol.29
, pp. 247-252
-
-
Kwan, S.-P.1
Hagemann, T.L.2
Blaese, R.M.3
Rosen, F.S.4
-
26
-
-
0027486438
-
The gene for autosomal dominant spinocerebellar ataxia (SCAI) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus
-
Kwiatkowski, T. J., Jr., Orr, H. T., Banfi, S., McCall, A. E., Jodice, C., Persichetti, F., Novelletto, A., LeBorgne-DeMarquoy, F., Divick, L. A., Frontali, M., Subramony, S. H., Beaudet, A. L., Terrenato, L., Zoghbi, H. Y., and Ranum, L. P. W. (1993). The gene for autosomal dominant Spinocerebellar Ataxia (SCAI) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus. Am. J. Hum. Genet. 53: 391-400.
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 391-400
-
-
Kwiatkowski T.J., Jr.1
Orr, H.T.2
Banfi, S.3
McCall, A.E.4
Jodice, C.5
Persichetti, F.6
Novelletto, A.7
LeBorgne-DeMarquoy, F.8
Divick, L.A.9
Frontali, M.10
Subramony, S.H.11
Beaudet, A.L.12
Terrenato, L.13
Zoghbi, H.Y.14
Ranum, L.P.W.15
-
27
-
-
0025918417
-
Physical mapping of 60 DNA markers in the p21.1-q21.3 region of the human X chromosome
-
Lafreniere, R. G., Brown, C. J., Powers, V. E., Carrel, L., Davies, K. E., Barker, D. F., and Willard, H. F. (1991). Physical mapping of 60 DNA markers in the p21.1-q21.3 region of the human X chromosome. Genomics 11: 352-363.
-
(1991)
Genomics
, vol.11
, pp. 352-363
-
-
Lafreniere, R.G.1
Brown, C.J.2
Powers, V.E.3
Carrel, L.4
Davies, K.E.5
Barker, D.F.6
Willard, H.F.7
-
28
-
-
0025334285
-
Rapid isolation of DNA probes within specific chromosome regions by interspersed repetitive sequences polymerase chain reaction
-
Ledbetter, S. A., Nelson, D. L., Warren, S. T., and Ledbetter, D. H. (1990). Rapid isolation of DNA probes within specific chromosome regions by interspersed repetitive sequences polymerase chain reaction. Genomics 6: 475-481.
-
(1990)
Genomics
, vol.6
, pp. 475-481
-
-
Ledbetter, S.A.1
Nelson, D.L.2
Warren, S.T.3
Ledbetter, D.H.4
-
29
-
-
0026725180
-
Fluorescence in situ hybridization of YAC clones after Alu-PCR amplification
-
Lengauer, C., Green, E. D., and Cremer, T. (1992). Fluorescence in situ hybridization of YAC clones after Alu-PCR amplification. Genomics 13: 826-828.
-
(1992)
Genomics
, vol.13
, pp. 826-828
-
-
Lengauer, C.1
Green, E.D.2
Cremer, T.3
-
30
-
-
0028358375
-
Physical linkage of expressed sequence tags (ESTs) to polymorphic markers on the X chromosome
-
Mazzarella, R., and Srivastava, A. K. (1994). Physical linkage of expressed sequence tags (ESTs) to polymorphic markers on the X chromosome. Hum. Mol. Genet. 3: 1095-1101.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1095-1101
-
-
Mazzarella, R.1
Srivastava, A.K.2
-
31
-
-
0342850276
-
Two novel genes mapped to cosmid contigs in Xp21.1 and Xp11.23
-
Meindl, A., de Carvalho, M. R. S., Schindelhauer, D., Herrmann, K., Grimm, L., Wehnert, M., Ross, M. T., and Meitinger, T. (1995). Two novel genes mapped to cosmid contigs in Xp21.1 and Xp11.23. Cytogenet. Cell Genet. 71: 340.
-
(1995)
Cytogenet. Cell Genet.
, vol.71
, pp. 340
-
-
Meindl, A.1
De Carvalho, M.R.S.2
Schindelhauer, D.3
Herrmann, K.4
Grimm, L.5
Wehnert, M.6
Ross, M.T.7
Meitinger, T.8
-
32
-
-
0023785183
-
Human ornithine-δ-aminotransferase
-
Mitchell, G. A., Looney, J. E., Brody, L. C., Steel, G., Suchanek, M., Engelhard, J. F., Willard, H. F., and Valle, D. (1988). Human ornithine-δ-aminotransferase. J. Biol. Chem. 263: 14288-14295.
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 14288-14295
-
-
Mitchell, G.A.1
Looney, J.E.2
Brody, L.C.3
Steel, G.4
Suchanek, M.5
Engelhard, J.F.6
Willard, H.F.7
Valle, D.8
-
33
-
-
0024756571
-
Assignment of the gene for complete X-linked Congenital Stationary Night Blindness (CSNB1) to Xp11.3
-
Musarella, M. A., Weleber, R. G., Murphey, W. H., Young, R. S. L., Anson-Cartwright, L., Mets, M., Kraft, S. P., Polemeno, R., Litt, M., and Worton, R. G. (1989). Assignment of the gene for complete X-linked Congenital Stationary Night Blindness (CSNB1) to Xp11.3. Genomics 5: 727-737.
-
(1989)
Genomics
, vol.5
, pp. 727-737
-
-
Musarella, M.A.1
Weleber, R.G.2
Murphey, W.H.3
Young, R.S.L.4
Anson-Cartwright, L.5
Mets, M.6
Kraft, S.P.7
Polemeno, R.8
Litt, M.9
Worton, R.G.10
-
34
-
-
0028114080
-
Characterization of four human YAC libraries for clone size, chimerism and X chromosome sequence representation
-
Nagaraja, R., Kere, J., MacMillan, S., Masisi, M. W. J., Johnson, D., Molini, B. J., Halley, G. R., Wein, K., Trusgnich, M., Eble, B., Railey, B., Brownstein, B. H., and Schlessinger, D. (1994). Characterization of four human YAC libraries for clone size, chimerism and X chromosome sequence representation. Nucleic Acids Res. 22: 3406-3411.
-
(1994)
Nucleic Acids Res.
, vol.22
, pp. 3406-3411
-
-
Nagaraja, R.1
Kere, J.2
MacMillan, S.3
Masisi, M.W.J.4
Johnson, D.5
Molini, B.J.6
Halley, G.R.7
Wein, K.8
Trusgnich, M.9
Eble, B.10
Railey, B.11
Brownstein, B.H.12
Schlessinger, D.13
-
35
-
-
0028868393
-
Report of the sixth international workshop on X chromosome mapping 1995
-
Nelson, D. L., Ballabio, A., Cremers, F., Monaco, A. P., and Schlessinger, D. (1995). Report of the sixth international workshop on X chromosome mapping 1995. Cytogenet. Cell Genet. 71: 307-342.
-
(1995)
Cytogenet. Cell Genet.
, vol.71
, pp. 307-342
-
-
Nelson, D.L.1
Ballabio, A.2
Cremers, F.3
Monaco, A.P.4
Schlessinger, D.5
-
36
-
-
0026345290
-
Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: Their potential as reference libraries
-
Nizetic, D., Zehetner, G., Monaco, A. P., Gellen, L., Young, B. D., and Lehrach, H. (1991). Construction, arraying, and high-density screening of large insert libraries of human chromosomes X and 21: Their potential as reference libraries. Proc. Natl. Acad. Sci. USA 88: 3233-3237.
-
(1991)
Proc. Natl. Acad. Sci. USA
, vol.88
, pp. 3233-3237
-
-
Nizetic, D.1
Zehetner, G.2
Monaco, A.P.3
Gellen, L.4
Young, B.D.5
Lehrach, H.6
-
37
-
-
0025190712
-
Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests
-
Ott, J., Bhattacharya, S., Chen, J. D., Denton, M. J., Donald, J., Dubay, C., Farrar, G. J., Fishman, G. A., Frey, D., Gal, A., Humphries, P., Jay, B., Jay, M., Litt, M., Machler, M., Musarella, M., Neugebauer, M., Nussbaum, R. L., Terwilliger, J. D., Weleber, R. G., Wirth, B., Wong, F., Worton, R. G., and Wright, A. F. (1990). Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests. Proc. Natl. Acad. Sci. USA 87: 701-704.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 701-704
-
-
Ott, J.1
Bhattacharya, S.2
Chen, J.D.3
Denton, M.J.4
Donald, J.5
Dubay, C.6
Farrar, G.J.7
Fishman, G.A.8
Frey, D.9
Gal, A.10
Humphries, P.11
Jay, B.12
Jay, M.13
Litt, M.14
Machler, M.15
Musarella, M.16
Neugebauer, M.17
Nussbaum, R.L.18
Terwilliger, J.D.19
Weleber, R.G.20
Wirth, B.21
Wong, F.22
Worton, R.G.23
Wright, A.F.24
more..
-
38
-
-
0025064534
-
Synaptophysin: Structure of the human gene and assignment to the X chromosome in man and mouse
-
Ozcelik, T., Lafreniere, R. G., Archer, B. T., Johnston, P. A., Willard, H. F., Francke, U., and Sudhof, T. C. (1990). Synaptophysin: Structure of the human gene and assignment to the X chromosome in man and mouse. Am. J. Hum. Genet. 47: 551-561.
-
(1990)
Am. J. Hum. Genet.
, vol.47
, pp. 551-561
-
-
Ozcelik, T.1
Lafreniere, R.G.2
Archer, B.T.3
Johnston, P.A.4
Willard, H.F.5
Francke, U.6
Sudhof, T.C.7
-
39
-
-
0027435571
-
Regional assignment of 19 X-linked ESTs
-
Parrish, J. E., and Nelson, D. L. (1993). Regional assignment of 19 X-linked ESTs. Hum. Mol. Genet. 2: 1901-1905.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1901-1905
-
-
Parrish, J.E.1
Nelson, D.L.2
-
40
-
-
0022884671
-
Regional localization of X chromosome short arm probes
-
Paulsen, K., Forrest, S., Scherer, G., Ropers, H.-H., and Davies, K. (1986). Regional localization of X chromosome short arm probes. Hum. Genet. 74: 155-159.
-
(1986)
Hum. Genet.
, vol.74
, pp. 155-159
-
-
Paulsen, K.1
Forrest, S.2
Scherer, G.3
Ropers, H.-H.4
Davies, K.5
-
41
-
-
0027268587
-
Chromosomal distribution of 320 genes from a brain cDNA library
-
Polymeropoulos, M. H., Xiao, H., Sikela, J. M., Adams, M., Venter, J. C., and Merril, C. R. (1993). Chromosomal distribution of 320 genes from a brain cDNA library. Nature Genet 4: 381-386.
-
(1993)
Nature Genet
, vol.4
, pp. 381-386
-
-
Polymeropoulos, M.H.1
Xiao, H.2
Sikela, J.M.3
Adams, M.4
Venter, J.C.5
Merril, C.R.6
-
42
-
-
0028601340
-
A YAC clone map spanning 7.5 megabases of human chromosome band Xq28
-
Rogner, U. C., Kioschis, P., Wilke, K., Gong, W., Pick, E., Dietrich, A., Lehrach, H., and Poustka, A. (1994). A YAC clone map spanning 7.5 megabases of human chromosome band Xq28. Hum. Mol. Genet. 3: 2137-2146.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 2137-2146
-
-
Rogner, U.C.1
Kioschis, P.2
Wilke, K.3
Gong, W.4
Pick, E.5
Dietrich, A.6
Lehrach, H.7
Poustka, A.8
-
43
-
-
0027401084
-
Dinucleotide repeat polymorphism at the DXS573 locus
-
Roustan, P., Curtis, A. R. J., Kamakari, S., Thiselton, D., Lindsay, S., and Bhattacharya, S. S. (1992). Dinucleotide repeat polymorphism at the DXS573 locus. Hum. Mol. Genet. 2: 92.
-
(1992)
Hum. Mol. Genet.
, vol.2
, pp. 92
-
-
Roustan, P.1
Curtis, A.R.J.2
Kamakari, S.3
Thiselton, D.4
Lindsay, S.5
Bhattacharya, S.S.6
-
44
-
-
0027177179
-
Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies
-
Scheinman, S. J., Pook, M. A., Wooding, C., Pang, J. T., Frymoyer, P. A., and Thakker, R. V. (1993). Mapping the gene causing X-linked recessive nephrolithiasis to Xp11.22 by linkage studies. J. Clin. Invest. 91: 2351-2357.
-
(1993)
J. Clin. Invest.
, vol.91
, pp. 2351-2357
-
-
Scheinman, S.J.1
Pook, M.A.2
Wooding, C.3
Pang, J.T.4
Frymoyer, P.A.5
Thakker, R.V.6
-
45
-
-
0025940605
-
Aland eye disease: Linkage data
-
Schwartz, M., and Rosenberg, T. (1991). Aland Eye Disease: Linkage data. Genomics 10: 327-332.
-
(1991)
Genomics
, vol.10
, pp. 327-332
-
-
Schwartz, M.1
Rosenberg, T.2
-
46
-
-
0028911437
-
Genetic and physical mapping of five novel microsatellite markers on human Xp21.1-p11.22
-
Thiselton, D. L., Lindsay, S., Kamakari, S., Hardcastle, A. J., Roustan, R., and Bhattacharya, S. S. (1995). Genetic and physical mapping of five novel microsatellite markers on human Xp21.1-p11.22. Genomics 25: 279-281.
-
(1995)
Genomics
, vol.25
, pp. 279-281
-
-
Thiselton, D.L.1
Lindsay, S.2
Kamakari, S.3
Hardcastle, A.J.4
Roustan, R.5
Bhattacharya, S.S.6
-
47
-
-
0343285018
-
Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1
-
Trump, D., Pilia, G., Dixon, P. H., Wooding, C., Thakrar, R., Leigh, S. E. A., Nagaraja, R., Whyte, M. P., Schlessinger, D., and Thakker, R. V. (1995). Construction of a YAC contig and an STS map spanning 3.6 megabase pairs in Xp22.1. Cytogenet. Cell Genet. 71: 337.
-
(1995)
Cytogenet. Cell Genet.
, vol.71
, pp. 337
-
-
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
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