-
1
-
-
0030842882
-
Abnormalities of chromosome band 8p11 in leukemia: Two clinical syndromes can be distinguished on the basis of MOZ involvement
-
Aguiar, R.C.T., Chase, A., Coulthard, S., Macdonald, D.H.C., Carapeti, M., Reiter, A., Sohal, J., Lennard, A., Goldman, J.M. & Cross, N.C.P. (1997) Abnormalities of chromosome band 8p11 in leukemia: two clinical syndromes can be distinguished on the basis of MOZ involvement. Blood, 90, 3130-3135.
-
(1997)
Blood
, vol.90
, pp. 3130-3135
-
-
Aguiar, R.C.T.1
Chase, A.2
Coulthard, S.3
Macdonald, D.H.C.4
Carapeti, M.5
Reiter, A.6
Sohal, J.7
Lennard, A.8
Goldman, J.M.9
Cross, N.C.P.10
-
2
-
-
13344259999
-
A comprehensive genetic map of the human genome based on 5264 microsatellites
-
Dib, C., Faure, S., Fizames, C., Samson, D., Drouot, N., Vignal, A., Millasseau, P., Marc, S., Hazan, J., Seboun, E., Lathrop, M., Gyapay, G., Morissette, J. & Weissenbach, J. (1996) A comprehensive genetic map of the human genome based on 5264 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
Lathrop, M.11
Gyapay, G.12
Morissette, J.13
Weissenbach, J.14
-
3
-
-
0030930177
-
Cytogenetic, fluorescence in situ hybridisation, and clinical evaluation of translocations with concomitant deletion at 13q14 in chronic lymphocytic leukaemia
-
Gardiner, A.C., Corcoran, M.M. & Oscier, D.G. (1997) Cytogenetic, fluorescence in situ hybridisation, and clinical evaluation of translocations with concomitant deletion at 13q14 in chronic lymphocytic leukaemia. Genes, Chromosomes and Cancer, 20, 73-81.
-
(1997)
Genes, Chromosomes and Cancer
, vol.20
, pp. 73-81
-
-
Gardiner, A.C.1
Corcoran, M.M.2
Oscier, D.G.3
-
4
-
-
0029149080
-
A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsyndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C)
-
Guilford, P., Dode, C., Crozet, F., Blanchard, S., Chaib, H., Levilliers, J., Levi-Acobas, F., Weil, D., Weissenbach, J., Cohen, D., Le Paslier, D., Kaplan, J.C. & Petit, C. (1995) A YAC contig and an EST map in the pericentromeric region of chromosome 13 surrounding the loci for neurosensory nonsyndromic deafness (DFNB1 and DFNA3) and limb-girdle muscular dystrophy type 2C (LGMD2C). Genomics, 29, 163-169.
-
(1995)
Genomics
, vol.29
, pp. 163-169
-
-
Guilford, P.1
Dode, C.2
Crozet, F.3
Blanchard, S.4
Chaib, H.5
Levilliers, J.6
Levi-Acobas, F.7
Weil, D.8
Weissenbach, J.9
Cohen, D.10
Le Paslier, D.11
Kaplan, J.C.12
Petit, C.13
-
5
-
-
0028869005
-
A new myeloproliferative disorder associated with chromosomal translocations involving 8p11: A review
-
Macdonald, D.. Aguiar, R.C., Mason, P.J., Goldman, J.M. & Cross, N.C. (1995) A new myeloproliferative disorder associated with chromosomal translocations involving 8p11: a review, Leukemia, 9, 1628-1630.
-
(1995)
Leukemia
, vol.9
, pp. 1628-1630
-
-
Macdonald, D.1
Aguiar, R.C.2
Mason, P.J.3
Goldman, J.M.4
Cross, N.C.5
-
6
-
-
0029032790
-
Karyotypic evolution in a granulocytic sarcoma developing in a myeloproliferative disorder with a novel (3;4) translocation
-
Myint, H., Chacko, J., Mould, S., Ross, F. & Oscier, D.G. (1995) Karyotypic evolution in a granulocytic sarcoma developing in a myeloproliferative disorder with a novel (3;4) translocation. British Journal of Haematology, 90, 462-464.
-
(1995)
British Journal of Haematology
, vol.90
, pp. 462-464
-
-
Myint, H.1
Chacko, J.2
Mould, S.3
Ross, F.4
Oscier, D.G.5
-
7
-
-
0028675056
-
Construction of cosmid libraries from flow-sorted human chromosomes 1, 6, 7, 11, 13, and 18 for reference library resources
-
Nizetic, D., Monard, S., Young, B., Cotter, F., Zehetner, G. & Lehrach, H. (1994) Construction of cosmid libraries from flow-sorted human chromosomes 1, 6, 7, 11, 13, and 18 for reference library resources. Mammalian Genome, 5, 801-802.
-
(1994)
Mammalian Genome
, vol.5
, pp. 801-802
-
-
Nizetic, D.1
Monard, S.2
Young, B.3
Cotter, F.4
Zehetner, G.5
Lehrach, H.6
-
8
-
-
0023726654
-
Translocation t(3;4)(q26;q21) in myelodysplastic syndrome with megakaryoblastic proliferation
-
Ohyashiki, K., Enomoto, Y., Watanabe, Y., Nehashi, Y., Ohyashiki, J.H. & Toyama, K. (1988) Translocation t(3;4)(q26;q21) in myelodysplastic syndrome with megakaryoblastic proliferation. Cancer, Genetics and Cytogenetics, 34, 5-9.
-
(1988)
Cancer, Genetics and Cytogenetics
, vol.34
, pp. 5-9
-
-
Ohyashiki, K.1
Enomoto, Y.2
Watanabe, Y.3
Nehashi, Y.4
Ohyashiki, J.H.5
Toyama, K.6
-
9
-
-
0030748326
-
Cytogenetic abnormalities and their prognostic significance in idiopathic myelofibrosis: A study of 106 cases
-
Reilly, J.T., Snowden, J.A., Spearing, R.L., Fitzgerald, P.M., Jones, N., Watmore, A. & Potter, A. (1997) Cytogenetic abnormalities and their prognostic significance in idiopathic myelofibrosis: a study of 106 cases. British Journal of Haematology, 98, 96-102.
-
(1997)
British Journal of Haematology
, vol.98
, pp. 96-102
-
-
Reilly, J.T.1
Snowden, J.A.2
Spearing, R.L.3
Fitzgerald, P.M.4
Jones, N.5
Watmore, A.6
Potter, A.7
-
10
-
-
0032170974
-
Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(p11:q12) myeloproliferative syndrome
-
Reiter, A., Sohal. J.. Kulkarni, S., Chase, A., Macdonald, D.H.C., Aguiar, R.C.T., Goncalves, C., Hernandez, J.M., Jennings, B.A., Goldman, J.M. & Cross, N.C.P. (1998) Consistent fusion of ZNF198 to the fibroblast growth factor receptor-1 in the t(8;13)(p11:q12) myeloproliferative syndrome. Blood, 92, 1735-1742.
-
(1998)
Blood
, vol.92
, pp. 1735-1742
-
-
Reiter, A.1
Sohal, J.2
Kulkarni, S.3
Chase, A.4
Macdonald, D.H.C.5
Aguiar, R.C.T.6
Goncalves, C.7
Hernandez, J.M.8
Jennings, B.A.9
Goldman, J.M.10
Cross, N.C.P.11
-
11
-
-
0031046448
-
Fine structure physical mapping of a 1-9 Mb region of chromosome 13q12
-
Still, I.H., Roberts, T. & Cowell. J.K. (1997) Fine structure physical mapping of a 1-9 Mb region of chromosome 13q12. Annals of Human Genetics, 61, 15-24.
-
(1997)
Annals of Human Genetics
, vol.61
, pp. 15-24
-
-
Still, I.H.1
Roberts, T.2
Cowell, J.K.3
-
12
-
-
0029916167
-
Small cell variant of Ki-1 lymphoma associated with myelofibrosis and a novel constitutional chromosomal translocation t(3;4)(q13;q12)
-
Yeo, W., Wong, N., Chow, J., Tsoi, W.C., Johnson, P.J. & Wickham, N. (1996) Small cell variant of Ki-1 lymphoma associated with myelofibrosis and a novel constitutional chromosomal translocation t(3;4)(q13;q12). Journal of Clinical Pathology, 49, 259-262.
-
(1996)
Journal of Clinical Pathology
, vol.49
, pp. 259-262
-
-
Yeo, W.1
Wong, N.2
Chow, J.3
Tsoi, W.C.4
Johnson, P.J.5
Wickham, N.6
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