-
1
-
-
0027730639
-
Definition and mapping of STSs at STR and RFLP loci in Xpll-Xq22
-
Barker, D. F., and Fain, P. M. (1993). Definition and mapping of STSs at STR and RFLP loci in Xpll-Xq22. Genomics 18: 712-716.
-
(1993)
Genomics
, vol.18
, pp. 712-716
-
-
Barker, D.F.1
Fain, P.M.2
-
2
-
-
0024670007
-
A method for generating hybrids containing nonselected fragments of human chromosomes
-
Benham, F., Hart, K., Crolla, J., Bobrow, M., Francavilla, M., and Goodfellow, P. M. (1989). A method for generating hybrids containing nonselected fragments of human chromosomes. Genomics 4: 509-517.
-
(1989)
Genomics
, vol.4
, pp. 509-517
-
-
Benham, F.1
Hart, K.2
Crolla, J.3
Bobrow, M.4
Francavilla, M.5
Goodfellow, P.M.6
-
3
-
-
0024530511
-
Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes
-
Cremers, F. P. M., van de Pol, D. J. R., Diergaarde, P. J., Wier- inga, B., Nussbaum, R. L., Schwartz, M., and Ropers, H. H. (1989). Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes. Genomics 4:41-46.
-
(1989)
Genomics
, vol.4
, pp. 41-46
-
-
Cremers, F.P.M.1
Van De Pol, D.J.R.2
Diergaarde, P.J.3
Wier-Inga, B.4
Nussbaum, R.L.5
Schwartz, M.6
Ropers, H.H.7
-
4
-
-
0025064847
-
Cloning of a gene that is rearranged in patients with choroideremia
-
Cremers, F. P. M., van de Pol, D. J. R., van Kerkhoff, L. P. M., Wieringa, B., and Ropers, H. H. (1990). Cloning of a gene that is rearranged in patients with choroideremia. Nature 347:674- 677.
-
(1990)
Nature
, vol.347
-
-
Cremers, F.P.M.1
Van De Pol, D.J.R.2
Van Kerkhoff, L.P.M.3
Wieringa, B.4
Ropers, H.H.5
-
5
-
-
11944250330
-
Two dinucleotide repeat polymorphisms at the DXS571 locus
-
Curtis, A. R. J., Roustan, P., Kamakari, S., Thiselton, D., Lindsay, S., and Bhattacharya, S. S. (1992). Two dinucleotide repeat polymorphisms at the DXS571 locus. Hum. Mol. Genet. 1: 776.
-
(1992)
Hum. Mol. Genet.
, vol.1
, pp. 776
-
-
Curtis, A.R.J.1
Roustan, P.2
Kamakari, S.3
Thiselton, D.4
Lindsay, S.5
Bhattacharya, S.S.6
-
6
-
-
0028988233
-
Association between X- linked mixed deafness and mutations in the POU domain gene brain 4
-
de Kok, Y. J. M., van der Maarel, S. M., Bitner-Glindzicz, M., Huber, I., Monaco, A. P., Malcolm, S., Pembrey, M. E., Ropers, H. H., and Cremers, F. P. M. (1995). Association between X- linked mixed deafness and mutations in the POU domain gene brain 4. Science 27: 685-688.
-
(1995)
Science
, vol.27
, pp. 685-688
-
-
De Kok, Y.J.M.1
Van Der Maarel, S.M.2
Bitner-Glindzicz, M.3
Huber, I.4
Monaco, A.P.5
Malcolm, S.6
Pembrey, M.E.7
Ropers, H.H.8
Cremers, F.P.M.9
-
7
-
-
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
-
8
-
-
0028388730
-
The brain-specific POU-box gene Brn4 is a sex-linked transcription factor located on the human and mouse X chromosomes
-
Douville, P. J., Atanasoski, S., Tobler, A., Fontana, A., and Schwab, M. E. (1994). The brain-specific POU-box gene Brn4 is a sex-linked transcription factor located on the human and mouse X chromosomes. Mamm. Genome 5: 180-182.
-
(1994)
Mamm. Genome
, vol.5
, pp. 180-182
-
-
Douville, P.J.1
Atanasoski, S.2
Tobler, A.3
Fontana, A.4
Schwab, M.E.5
-
9
-
-
0028231090
-
The 1993-94 Genethon human genetic linkage map
-
Gyapay, G., Morissette, J., Vignal, A., Dib, C., Fizames, C., Millasseau, P., Marc, S., Bernardi, G., Lathrop, M., and Weissenbach, J. (1994). The 1993-94 Genethon 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
Millasseau, P.6
Marc, S.7
Bernardi, G.8
Lathrop, M.9
Weissenbach, J.10
-
10
-
-
0027849627
-
X-linked a thalassemia/mental retardation syndrome: Analysis in a new family further supports localization in proximal Xq
-
Houdayer, C., Toutain, A., Ronce, N., Lefort, G., Sarda, P., Taib, J., Briault, S., Lambert, J. C., and Moraine, C. (1993). X-linked a thalassemia/mental retardation syndrome: Analysis in a new family further supports localization in proximal Xq. Ann. Genet. 36: 194-199.
-
(1993)
Ann. Genet.
, vol.36
, pp. 194-199
-
-
Houdayer, C.1
Toutain, A.2
Ronce, N.3
Lefort, G.4
Sarda, P.5
Taib, J.6
Briault, S.7
Lambert, J.C.8
Moraine, C.9
-
11
-
-
0028334226
-
X-linked mixed deafness (DFN3): Cloning and characterization of the critical region allows the identification of novel microdeletions
-
Huber, I., Bitner-Glindzicz, M., de Kok, Y. J. M., van de Maarel, S. M., Ishikawa-Brush, Y., Monaco, A. P., Robinson, D., Malcolm, S., Pembrey, E., Brunner, H. G., Cremers, F. P. M., and Ropers, H. H. (1994). X-linked mixed deafness (DFN3): Cloning and characterization of the critical region allows the identification of novel microdeletions. Hum. Mol. Genet. 3: 1151-1154.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1151-1154
-
-
Huber, I.1
Bitner-Glindzicz, M.2
De Kok, Y.J.M.3
Van De Maarel, S.M.4
Ishikawa-Brush, Y.5
Monaco, A.P.6
Robinson, D.7
Malcolm, S.8
Pembrey, E.9
Brunner, H.G.10
Cremers, F.P.M.11
Ropers, H.H.12
-
12
-
-
0026736249
-
Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms
-
Hudson, T. J., Engelstein, M., Lee, M. K, Ho, E. C., Rubenfield, M. J., Adams, C. P., Housman, D. E., and Dracopoli, N. C. (1992). Isolation and chromosomal assignment of 100 highly informative human simple sequence repeat polymorphisms. Genomics 13: 622-629.
-
(1992)
Genomics
, vol.13
, pp. 622-629
-
-
Hudson, T.J.1
Engelstein, M.2
Lee, M.K.3
Ho, E.C.4
Rubenfield, M.J.5
Adams, C.P.6
Housman, D.E.7
Dracopoli, N.C.8
-
13
-
-
0027209471
-
Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosome
-
Lindsay, S., Curtis, A. J. R., Roustan, P., Kamakari, S., Thisel- ton, D. L., Stephenson, A., and Battacharya, S. S. (1993). Isolation and characterization of three microsatellite markers in the proximal long arm of the human X chromosome. Genomics 17: 208-210.
-
(1993)
Genomics
, vol.17
, pp. 208-210
-
-
Lindsay, S.1
Curtis, A.J.R.2
Roustan, P.3
Kamakari, S.4
Thisel-Ton, D.L.5
Stephenson, A.6
Battacharya, S.S.7
-
14
-
-
0025273118
-
Five polymorphic microsatellite VNTRs on the human X chromosome
-
Luty, J. A., Guo, Z., Willard, H. F., Ledbetter, D. H., Ledbetter, S., and Litt, M. (1990). Five polymorphic microsatellite VNTRs on the human X chromosome. Am. J. Hum. Genet. 46: 776-783.
-
(1990)
Am. J. Hum. Genet
, vol.46
, pp. 776-783
-
-
Luty, J.A.1
Guo, Z.2
Willard, H.F.3
Ledbetter, D.H.4
Ledbetter, S.5
Litt, M.6
-
15
-
-
0026529434
-
Isolation of a candidate gene for choroideremia
-
Merry, D. E., Janne, P. A., Landers, J. E., Lewis, R. A., and Nussbaum, R. L. (1992). Isolation of a candidate gene for choroideremia. Proc. Natl. Acad. Sci. USA 89: 2135-2139.
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 2135-2139
-
-
Merry, D.E.1
Janne, P.A.2
Landers, J.E.3
Lewis, R.A.4
Nussbaum, R.L.5
-
16
-
-
0027283764
-
Physical mapping of DNA markers in the ql3-q22 region of the human X chromosome
-
Philippe, C., Cremers, F. P. M., Chery, M., Bach, I., Abbadi, N., Ropers, H. H., and Gilgenkrantz, S. (1993). Physical mapping of DNA markers in the ql3-q22 region of the human X chromosome. Genomics 17: 147-152.
-
(1993)
Genomics
, vol.17
, pp. 147-152
-
-
Philippe, C.1
Cremers, F.P.M.2
Chery, M.3
Bach, I.4
Abbadi, N.5
Ropers, H.H.6
Gilgenkrantz, S.7
-
17
-
-
0026447017
-
The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xpll.2-Xql3)
-
Porteus, M. E. M., Curtis, A., Lindsay, S., Williams, O., Goudie, D., Kamakari, S., and Bhattacharya, S. S. (1992). The gene for Aarskog syndrome is located between DXS255 and DXS566 (Xpll.2-Xql3). Genomics 14: 298-301.
-
(1992)
Genomics
, vol.14
, pp. 298-301
-
-
Porteus, M.E.M.1
Curtis, A.2
Lindsay, S.3
Williams, O.4
Goudie, D.5
Kamakari, S.6
Bhattacharya, S.S.7
-
18
-
-
0026596195
-
Dinucleotide repeat polymorphism at the DXS441 locus
-
Ram, K. T., Barker, D. F., and Puck, J. M. (1992). Dinucleotide repeat polymorphism at the DXS441 locus. Nucleic Acids Res. 20: 1428.
-
(1992)
Nucleic Acids Res
, vol.20
, pp. 1428
-
-
Ram, K.T.1
Barker, D.F.2
Puck, J.M.3
-
19
-
-
12044253625
-
Primers for the dinucleotide repeat at the DXS453 locus also recognize the DXS983 locus
-
Rider, S. H., and Monaco, A. P. (1993). Primers for the dinucleotide repeat at the DXS453 locus also recognize the DXS983 locus. Hum. Mol. Genet. 2: 1510.
-
(1993)
Hum. Mol. Genet.
, vol.2
, pp. 1510
-
-
Rider, S.H.1
Monaco, A.P.2
-
20
-
-
0027440973
-
The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xql2-q21)
-
Saugier-Veber, P., Abadie, V., Moncla, A., Mathieu, M., Puis- san, C., Turleau, C., Mattei, J. F., Munnich, A., and Lyonnet, S. (1993). The Juberg-Marsidi syndrome maps to the proximal long arm of the X chromosome (Xql2-q21). Am. J. Hum. Genet. 52: 1040-1045.
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 1040-1045
-
-
Saugier-Veber, P.1
Abadie, V.2
Moncla, A.3
Mathieu, M.4
Puis-San, C.5
Turleau, C.6
Mattei, J.F.7
Munnich, A.8
Lyonnet, S.9
-
21
-
-
19144365441
-
Allan-Herndon-Dudley syndrome, linkage analysis in a third family and refinement of the localization in Xq21
-
Schwartz, C. E., Martin, J., Ouzts, L., Arena, J. F., Lubs, A. H., and Stevenson, R. E. (1994). Allan-Herndon-Dudley syndrome, linkage analysis in a third family and refinement of the localization in Xq21. Cytogenet. Cell Genet. 67: 351.
-
(1994)
Cytogenet. Cell Genet.
, vol.67
, pp. 351
-
-
Schwartz, C.E.1
Martin, J.2
Ouzts, L.3
Arena, J.F.4
Lubs, A.H.5
Stevenson, R.E.6
-
22
-
-
85027590662
-
Physical mapping of the X-linked cleft palate locus
-
Stanier, P., Forbes, S., Richardson, M., Brennan, L., Cole, C. G., Bentley, D. R., and Moore, G. E. (1994). Physical mapping of the X-linked cleft palate locus. Cytogenet. Cell Genet. 67:351-352.
-
(1994)
Cytogenet. Cell Genet.
, vol.67
, pp. 351-352
-
-
Stanier, P.1
Forbes, S.2
Richardson, M.3
Brennan, L.4
Cole, C.G.5
Bentley, D.R.6
Moore, G.E.7
-
23
-
-
0028237921
-
Cloning and characterization of the human choroideremia gene
-
van Bokhoven, H., van den Hurk, J., Bogerd, L., Philippe, C., Gilgenkrantz, S., de Jong, P., Ropers, H. H., and Cremers, F. P. M. (1994). Cloning and characterization of the human choroideremia gene. Hum. Mol. Genet. 3: 1041-1046.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1041-1046
-
-
Van Bokhoven, H.1
Van Den Hurk, J.2
Bogerd, L.3
Philippe, C.4
Gilgenkrantz, S.5
De Jong, P.6
Ropers, H.H.7
Cremers, F.P.M.8
-
24
-
-
0028285493
-
Mutation spectrum in the CHM gene of Danish and Swedish choroideremia patients
-
van Bokhoven, H., Schwartz, M., Andréasson, S., van den Hurk, A. J. M., Bogerd, L., Jay, M., Ruther, K., Jay, B., Pawlowitzki, I. H., Sankila, E. M., Wright, A., Ropers, H. H., Rosenberg, T., and Cremers, F. P. M. (1994). Mutation spectrum in the CHM gene of Danish and Swedish choroideremia patients. Hum. Mol. Genet. 3: 1047-1051.
-
(1994)
Hum. Mol. Genet.
, vol.3
, pp. 1047-1051
-
-
Van Bokhoven, H.1
Schwartz, M.2
Andréasson, S.3
Van Den Hurk, A.J.M.4
Bogerd, L.5
Jay, M.6
Ruther, K.7
Jay, B.8
Pawlowitzki, I.H.9
Sankila, E.M.10
Wright, A.11
Ropers, H.H.12
Rosenberg, T.13
Cremers, F.P.M.14
-
25
-
-
0025371201
-
Dinucleotide repeat polymorphisms at the DXS453, DXS454 and DXS458 loci
-
Weber, J. L., Kwitek, A. E., May, P. E., Polymeropoulos, M. H., and Ledbetter, S. (1990). Dinucleotide repeat polymorphisms at the DXS453, DXS454 and DXS458 loci. Nucleic Acids Res. 18: 4037.
-
(1990)
Nucleic Acids Res
, vol.18
, pp. 4037
-
-
Weber, J.L.1
Kwitek, A.E.2
May, P.E.3
Polymeropoulos, M.H.4
Ledbetter, S.5
-
26
-
-
0027936475
-
Report of the fifth international workshop on human X chromosome mapping 1994
-
Willard, H. F., Cremers, F. P. M., Mandel, J. L., Monaco, A. P., Nelson, D. L., and Schlessinger, D. (1994). Report of the fifth international workshop on human X chromosome mapping 1994. Cytogenet. Cell Genet. 67: 295-358.
-
(1994)
Cytogenet. Cell Genet.
, vol.67
, pp. 295-358
-
-
Willard, H.F.1
Cremers, F.P.M.2
Mandel, J.L.3
Monaco, A.P.4
Nelson, D.L.5
Schlessinger, D.6
|