-
1
-
-
0033068058
-
The impact of the new fish technologies on the cytogenetics of haematological malignancies
-
Kearney L: The impact of the new fish technologies on the cytogenetics of haematological malignancies. Br J Haematol 4: 648-658, 1999.
-
(1999)
Br J Haematol
, vol.4
, pp. 648-658
-
-
Kearney, L.1
-
2
-
-
0037202151
-
Molecular cytogenetic aspects of hematologic malignancies: Clinical implications
-
Chen Z and Sanderbrg AA: Molecular cytogenetic aspects of hematologic malignancies: clinical implications. Am J Med Genet 115: 130-141, 2002.
-
(2002)
Am J Med Genet
, vol.115
, pp. 130-141
-
-
Chen, Z.1
Sanderbrg, A.A.2
-
3
-
-
0032784783
-
World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: Report of the Clinical Advisory Committee meeting-Airlie House, Virginia
-
Harris NL, Jaffe ES, Diebold J, Frandrin G, Muller-Hermelink HK, Vardiman J, Lister TA and Bloomfield CD: World Health Organization classification of neoplastic diseases of the hematopoietic and lymphoid tissues: report of the Clinical Advisory Committee meeting-Airlie House, Virginia. Clin Oncol 17: 3835-3849, 1997.
-
(1997)
Clin Oncol
, vol.17
, pp. 3835-3849
-
-
Harris, N.L.1
Jaffe, E.S.2
Diebold, J.3
Frandrin, G.4
Muller-Hermelink, H.K.5
Vardiman, J.6
Lister, T.A.7
Bloomfield, C.D.8
-
4
-
-
0003477486
-
-
Lyon, IARC Press
-
Jaffe ES, Harris NL, Stein H, Vardiman JW (eds.): World Health Organization Classification of Tumours. Pathology and genetics of tumours of haematopoietic and lymphoid tissues. Lyon, IARC Press, 2001.
-
(2001)
World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Haematopoietic and Lymphoid Tissues
-
-
Jaffe, E.S.1
Harris, N.L.2
Stein, H.3
Vardiman, J.W.4
-
5
-
-
0036786901
-
The World Health Organization (WHO) classification of the myeloid neoplasms
-
Vardiman JW, Harris NL and Brunning RD: The World Health Organization (WHO) classification of the myeloid neoplasms. Blood 100: 2292-2302, 2002.
-
(2002)
Blood
, vol.100
, pp. 2292-2302
-
-
Vardiman, J.W.1
Harris, N.L.2
Brunning, R.D.3
-
6
-
-
0021264226
-
Fourth International Workshop on Chromosomes in Leukemia: Clinical significance of chromosomal abnormalities in acute non lymphoblastic leukemia
-
Bloomfield CD, Goldman A, Hossfeld D and de la Chapelle A: Fourth International Workshop on Chromosomes in Leukemia: clinical significance of chromosomal abnormalities in acute non lymphoblastic leukemia. Cancer Genet Cytogenet 11: 332-350, 1984.
-
(1984)
Cancer Genet Cytogenet
, vol.11
, pp. 332-350
-
-
Bloomfield, C.D.1
Goldman, A.2
Hossfeld, D.3
De La Chapelle, A.4
-
7
-
-
0034758836
-
The clinical significance of cytogenetic abnormalities in acute myeloid leukemia
-
Grimwade D: The clinical significance of cytogenetic abnormalities in acute myeloid leukemia. Best Pract Res Clin Haematol 14: 497-529, 2001.
-
(2001)
Best Pract Res Clin Haematol
, vol.14
, pp. 497-529
-
-
Grimwade, D.1
-
8
-
-
0035339877
-
Comparison of cytogenetic and molecular genetic detection of t (8;21) and inv (16) in a prospective series of adults with de novo acute myeloid leukemia: A Cancer and Leukemia Group B study
-
Mrozek K, Prior TW, Edwards C et al: Comparison of cytogenetic and molecular genetic detection of t (8;21) and inv (16) in a prospective series of adults with de novo acute myeloid leukemia: a Cancer and Leukemia Group B study. J Clin Oncol 19: 2482-2492, 2001.
-
(2001)
J Clin Oncol
, vol.19
, pp. 2482-2492
-
-
Mrozek, K.1
Prior, T.W.2
Edwards, C.3
-
9
-
-
0037269184
-
Acute myeloid leukemia with MLL rearrangements: Clinicobiological features, prognostic impact and value of flowcytometry in the detection of residual leukemic cells
-
Minoz L, Nomded JF, Villamor N et al: Acute myeloid leukemia with MLL rearrangements: clinicobiological features, prognostic impact and value of flowcytometry in the detection of residual leukemic cells. Leukemia 17: 76-82, 2003.
-
(2003)
Leukemia
, vol.17
, pp. 76-82
-
-
Minoz, L.1
Nomded, J.F.2
Villamor, N.3
-
10
-
-
0015246254
-
A rapid banding technique for human chromosomes
-
Seabright M: A rapid banding technique for human chromosomes. Lancet 30: 971-972, 1971
-
(1971)
Lancet
, vol.30
, pp. 971-972
-
-
Seabright, M.1
-
11
-
-
0017258328
-
High resolution of human chromosomes
-
Yunis JG: High resolution of human chromosomes. Science 26: 1268-1270, 1976.
-
(1976)
Science
, vol.26
, pp. 1268-1270
-
-
Yunis, J.G.1
-
12
-
-
0001745242
-
Molecular cytogenetics of contiguous gene syndromes: Mechanisms and consequences of gene dosage imbalance
-
Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Kinzler KW, Vogelstein B (eds.) MacGraw Hill, New York, NY, Chap. 65
-
Shaffer LG, Ledbetter DH and Lupski JR: Molecular cytogenetics of contiguous gene syndromes: mechanisms and consequences of gene dosage imbalance. In: Scriver CR, Beaudet AL, Sly WS, Valle D, Childs B, Kinzler KW, Vogelstein B (eds.) Metabolic and Molecular Basis of Inherited Disease, 8th edition, MacGraw Hill, New York, NY, Chap. 65, 1999.
-
(1999)
Metabolic and Molecular Basis of Inherited Disease, 8th Edition
-
-
Shaffer, L.G.1
Ledbetter, D.H.2
Lupski, J.R.3
-
14
-
-
0022916663
-
Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: Detection of trisomy 18 with probe L1. 84
-
Cremer T, Landegent J and Bruckner A: Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: detection of trisomy 18 with probe L1. 84. Human Genetics 74: 346-352, 1986.
-
(1986)
Human Genetics
, vol.74
, pp. 346-352
-
-
Cremer, T.1
Landegent, J.2
Bruckner, A.3
-
15
-
-
0029843439
-
Deciding and validation of DNA probe sets for a comprehensive interphase cytogenetic analysis of acute myeloid leukemia
-
Fischer K, Scholl C, Salat J, Frohling S, Schénk K, Bentz M, Stilgenbauer S, Lichter P and Dohner H: Deciding and validation of DNA probe sets for a comprehensive interphase cytogenetic analysis of acute myeloid leukemia. Blood 88: 3962-3971, 1996.
-
(1996)
Blood
, vol.88
, pp. 3962-3971
-
-
Fischer, K.1
Scholl, C.2
Salat, J.3
Frohling, S.4
Schénk, K.5
Bentz, M.6
Stilgenbauer, S.7
Lichter, P.8
Dohner, H.9
-
16
-
-
0026533307
-
Detection of trisomy 12 in chronic lymphocytic leukemia by fluorescence in situ hybridization to interphase cells: A simple and sensitive method
-
Anastasi J, Le Beau MM, Vardiman JW, Fernald AA, Larson RA and Rowley JD: Detection of trisomy 12 in chronic lymphocytic leukemia by fluorescence in situ hybridization to interphase cells: a simple and sensitive method. Blood 79: 1796-1801, 1992.
-
(1992)
Blood
, vol.79
, pp. 1796-1801
-
-
Anastasi, J.1
Le Beau, M.M.2
Vardiman, J.W.3
Fernald, A.A.4
Larson, R.A.5
Rowley, J.D.6
-
18
-
-
0029099360
-
Heterogeneity of deletions involving RB-1 and the D13S25 locus in B-cell chronic lymphocytic leukemia revealed by fluorescence in situ hybridization
-
Stilgenbauer S, Leupolt E, Ohl S, Weiss G, Schröder M, Fischer K, Bentz M, Lichter P and Döhner H: Heterogeneity of deletions involving RB-1 and the D13S25 locus in B-cell chronic lymphocytic leukemia revealed by fluorescence in situ hybridization. Cancer Res 55: 3475-3477, 1995.
-
(1995)
Cancer Res
, vol.55
, pp. 3475-3477
-
-
Stilgenbauer, S.1
Leupolt, E.2
Ohl, S.3
Weiss, G.4
Schröder, M.5
Fischer, K.6
Bentz, M.7
Lichter, P.8
Döhner, H.9
-
19
-
-
0027457275
-
High frequency of monoallelic retinoblastoma gene deletion in B-cell chronic lymphoid leukemia shown by interphase cytogenetics
-
Stilgenbauer S, Dohner H, Bulgay-Morschel M, Weitz S, Bentz M and Lichter P: High frequency of monoallelic retinoblastoma gene deletion in B-cell chronic lymphoid leukemia shown by interphase cytogenetics. Blood 81: 2118-2124, 1993.
-
(1993)
Blood
, vol.81
, pp. 2118-2124
-
-
Stilgenbauer, S.1
Dohner, H.2
Bulgay-Morschel, M.3
Weitz, S.4
Bentz, M.5
Lichter, P.6
-
20
-
-
0028987180
-
p53 gene deletion predicts for poor survival and non-response to therapy with purine analogs in chronic B-cell leukemias
-
Döhner H, Fischer K, Bentz M, Hansen K, Benner A, Cabot G, Diehl D, Schlenk R, Coy J, Stilgenbauer S, Volkmann M, Galle PR, Poustka A, Hunstein W and Lichter P: p53 gene deletion predicts for poor survival and non-response to therapy with purine analogs in chronic B-cell leukemias. Blood 85: 1580-1589, 1995.
-
(1995)
Blood
, vol.85
, pp. 1580-1589
-
-
Döhner, H.1
Fischer, K.2
Bentz, M.3
Hansen, K.4
Benner, A.5
Cabot, G.6
Diehl, D.7
Schlenk, R.8
Coy, J.9
Stilgenbauer, S.10
Volkmann, M.11
Galle, P.R.12
Poustka, A.13
Hunstein, W.14
Lichter, P.15
-
21
-
-
0030248425
-
Trisomy 12 and p53 deletion in chronic lymphocytic leukemia detected by fluorescence in situ hybridization: Association with morphology and resistance to conventional chemotherapy
-
Cano I, Martinez J, Quevedo E, Pinilla J, Martin-Recio A, Rodriguez A, Castaneda A, Lopez R, Perez-Pino T and Hernandez-Navarro F: Trisomy 12 and p53 deletion in chronic lymphocytic leukemia detected by fluorescence in situ hybridization: association with morphology and resistance to conventional chemotherapy. Cancer Genet Cytogenet 90: 118-124, 1996.
-
(1996)
Cancer Genet Cytogenet
, vol.90
, pp. 118-124
-
-
Cano, I.1
Martinez, J.2
Quevedo, E.3
Pinilla, J.4
Martin-Recio, A.5
Rodriguez, A.6
Castaneda, A.7
Lopez, R.8
Perez-Pino, T.9
Hernandez-Navarro, F.10
-
22
-
-
0030797830
-
Biallelic mutations in the ATM gene in T-prolymphocytic leukemia
-
Stilgenbauer S, Schaffner C, Litterst A, Liebisch P, Gilad S, Bar-Shira A, James MR, Lichter P and Dohner H: Biallelic mutations in the ATM gene in T-prolymphocytic leukemia. Nature Med 3: 1155-1159, 1997.
-
(1997)
Nature Med
, vol.3
, pp. 1155-1159
-
-
Stilgenbauer, S.1
Schaffner, C.2
Litterst, A.3
Liebisch, P.4
Gilad, S.5
Bar-Shira, A.6
James, M.R.7
Lichter, P.8
Dohner, H.9
-
23
-
-
0026023565
-
Interphase cytogenetic analysis detects minimal residual disease in a case of acute lymphoblastic leukemia and resolves the question of relapse after allogeneic bone marrow transplantation
-
Anastasi J, Thangavely M, Vardiman JW, Hooberman AL, Bian ML, Larson RA and Le Beau MM: Interphase cytogenetic analysis detects minimal residual disease in a case of acute lymphoblastic leukemia and resolves the question of relapse after allogeneic bone marrow transplantation. Blood 77: 1087-1091, 1991.
-
(1991)
Blood
, vol.77
, pp. 1087-1091
-
-
Anastasi, J.1
Thangavely, M.2
Vardiman, J.W.3
Hooberman, A.L.4
Bian, M.L.5
Larson, R.A.6
Le Beau, M.M.7
-
24
-
-
0027401551
-
Detection of residual host cells after bone marrow transplantation using non-isotopic in situ hybridisation and karyotype analysis
-
Wessman M, Popp S, Ruutu T, Volin L, Cremer T and Knuutila S: Detection of residual host cells after bone marrow transplantation using non-isotopic in situ hybridisation and karyotype analysis. Bone Marrow Transplant 11: 279-284, 1993.
-
(1993)
Bone Marrow Transplant
, vol.11
, pp. 279-284
-
-
Wessman, M.1
Popp, S.2
Ruutu, T.3
Volin, L.4
Cremer, T.5
Knuutila, S.6
-
25
-
-
0030974970
-
Increased sensitivity of minimal residual disease detection by interphase FISH in acute lymphoblastic leukemia with hyperdiploidy
-
Kasprzyk A and Seeker-Walker LM: Increased sensitivity of minimal residual disease detection by interphase FISH in acute lymphoblastic leukemia with hyperdiploidy. Leukemia 11: 429-135, 1997.
-
(1997)
Leukemia
, vol.11
, pp. 429-1135
-
-
Kasprzyk, A.1
Seeker-Walker, L.M.2
-
26
-
-
0026736660
-
Simultaneous genotypic and immunophenotypic analysis of interphase cells using dual-colour fluorescence: A demonstration of lineage involvement in polycythemia vera
-
Price CM, Kanfer EJ, Colman SM, Westwood N, Barret AJ and Greaves MF: Simultaneous genotypic and immunophenotypic analysis of interphase cells using dual-colour fluorescence: a demonstration of lineage involvement in polycythemia vera. Blood 80: 1033-1038, 1992.
-
(1992)
Blood
, vol.80
, pp. 1033-1038
-
-
Price, C.M.1
Kanfer, E.J.2
Colman, S.M.3
Westwood, N.4
Barret, A.J.5
Greaves, M.F.6
-
27
-
-
0027524856
-
Cell lineage involvement in four patients with myelodysplastic syndrome and t (1;7) or trisomy 8 studied by simultaneous immunophenotyping and fluorescence in situ hybridization
-
Nylund SJ, Verbeek W, Larramendy ML, Ruutu T, Heinonen K, Hallman H and Knuutila S: Cell lineage involvement in four patients with myelodysplastic syndrome and t (1;7) or trisomy 8 studied by simultaneous immunophenotyping and fluorescence in situ hybridization. Cancer Genet Cytogenet 70: 120-124, 1993.
-
(1993)
Cancer Genet Cytogenet
, vol.70
, pp. 120-124
-
-
Nylund, S.J.1
Verbeek, W.2
Larramendy, M.L.3
Ruutu, T.4
Heinonen, K.5
Hallman, H.6
Knuutila, S.7
-
28
-
-
0027984279
-
Direct detection of the Philadelphia chromosome in CD20-positive lymphocytes in chronic myeloid leukemia by tri-color immunophenotyping/FISH
-
Torlakovic E, Litz CE, McClure JS and Brunning RD: Direct detection of the Philadelphia chromosome in CD20-positive lymphocytes in chronic myeloid leukemia by tri-color immunophenotyping/FISH. Leukemia 8: 1940-1943, 1994.
-
(1994)
Leukemia
, vol.8
, pp. 1940-1943
-
-
Torlakovic, E.1
Litz, C.E.2
McClure, J.S.3
Brunning, R.D.4
-
29
-
-
0029032664
-
Combined immunophenotying and in situ hybridization (FICTION): A rapid method to study cell lineage involvment in myelodysplastic syndromes
-
Soenen V, Fenaux P, Flactif M, Lepelley P, Lai JL, Cosson A and Preudhomme C: Combined immunophenotying and in situ hybridization (FICTION): a rapid method to study cell lineage involvment in myelodysplastic syndromes. Br J Haematol 90: 701-706, 1995.
-
(1995)
Br J Haematol
, vol.90
, pp. 701-706
-
-
Soenen, V.1
Fenaux, P.2
Flactif, M.3
Lepelley, P.4
Lai, J.L.5
Cosson, A.6
Preudhomme, C.7
-
30
-
-
0006701543
-
Which compartments are involved in Philadelphia-chromosome positive chronic myeloid leukemia? An answer at the single cell level by combining May-Grunwald-Giemsa staining and fluorescence in situ hybridization techniques
-
Haferlach T, Winkemann M, Nickenig C, Meeder M., Ramm-Petersen L, Schoch R, Nickelsen M, Weber-Matthiesen K, Schlegelberger B, Schoch C, Nickelsen M, Weber-Mathiesen K, Schlegelberger B, Schoch C, Gassmann W and Löffler H: Which compartments are involved in Philadelphia-chromosome positive chronic myeloid leukemia? An answer at the single cell level by combining May-Grunwald-Giemsa staining and fluorescence in situ hybridization techniques. Br J Haematol 97: 99-106, 1997.
-
(1997)
Br J Haematol
, vol.97
, pp. 99-106
-
-
Haferlach, T.1
Winkemann, M.2
Nickenig, C.3
Meeder, M.4
Ramm-Petersen, L.5
Schoch, R.6
Nickelsen, M.7
Weber-Matthiesen, K.8
Schlegelberger, B.9
Schoch, C.10
Nickelsen, M.11
Weber-Mathiesen, K.12
Schlegelberger, B.13
Schoch, C.14
Gassmann, W.15
Löffler, H.16
-
31
-
-
0027494194
-
Leukaemia arising in donor cells following allegeneic bone marrow transplantation for thalassaemia demonstrated by immunological, DNA and cytogenetic analysis
-
Katz F, Reeves BR, Alexander S, Kearney L and Chessells J: Leukaemia arising in donor cells following allegeneic bone marrow transplantation for thalassaemia demonstrated by immunological, DNA and cytogenetic analysis. Br J Haematol 85: 326-331, 1993.
-
(1993)
Br J Haematol
, vol.85
, pp. 326-331
-
-
Katz, F.1
Reeves, B.R.2
Alexander, S.3
Kearney, L.4
Chessells, J.5
-
33
-
-
0026345679
-
Construction and characterization of plasmid libraries enriched in sequences from single human chromosomes
-
Collins C, Kuo WL, Segraves R, Fuscoe J, Pinkel D and Gray JW: Construction and characterization of plasmid libraries enriched in sequences from single human chromosomes. Genomics 11: 997-1006, 1991.
-
(1991)
Genomics
, vol.11
, pp. 997-1006
-
-
Collins, C.1
Kuo, W.L.2
Segraves, R.3
Fuscoe, J.4
Pinkel, D.5
Gray, J.W.6
-
34
-
-
0026587345
-
Cytogenetic analysis by chromosome painting using degenerate oligonucleotide-primed-polymerase chain reaction amplified flow-sorted chromosomes
-
Telenius H, Pelmear AH, Tunnacliffe A, Carter NP, Behmel A, Ferguson-Smith MA, Nordenskjold M, Pfragner R and Ponder BAJ: Cytogenetic analysis by chromosome painting using degenerate oligonucleotide-primed- polymerase chain reaction amplified flow-sorted chromosomes. Genes Chrom Cancer 4: 257-263, 1992.
-
(1992)
Genes Chrom Cancer
, vol.4
, pp. 257-263
-
-
Telenius, H.1
Pelmear, A.H.2
Tunnacliffe, A.3
Carter, N.P.4
Behmel, A.5
Ferguson-Smith, M.A.6
Nordenskjold, M.7
Pfragner, R.8
Ponder, B.A.J.9
-
35
-
-
0027365062
-
Libraries for each human chromosome, constructed from sorter-enriched chromosomes by using linker-adaptor PCR
-
Vooijs M, Yu LC, Tkachuk D, Pinkel D, Johnson D and Gray JW: Libraries for each human chromosome, constructed from sorter-enriched chromosomes by using linker-adaptor PCR. Am J Hum Genet 52: 586-597, 1993.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 586-597
-
-
Vooijs, M.1
Yu, L.C.2
Tkachuk, D.3
Pinkel, D.4
Johnson, D.5
Gray, J.W.6
-
36
-
-
0029684940
-
Chromosome arm painting probes
-
Guan XY, Zhang H, Bittner M, Jiang Y, Meltzer P and Trent VJ: Chromosome arm painting probes. Nat Genet 12: 10-11, 1996.
-
(1996)
Nat Genet
, vol.12
, pp. 10-11
-
-
Guan, X.Y.1
Zhang, H.2
Bittner, M.3
Jiang, Y.4
Meltzer, P.5
Trent, V.J.6
-
37
-
-
0026948875
-
Multiple colors by fluorescence in situ hybridization using radiolabelled DNA probes create a molecular karyotype
-
Dauwerse JG, Wiegant J, Raap AK, Breuning MH and van Ommen GJB: Multiple colors by fluorescence in situ hybridization using radiolabelled DNA probes create a molecular karyotype. Hum Mol Genet 1: 593-598, 1992.
-
(1992)
Hum Mol Genet
, vol.1
, pp. 593-598
-
-
Dauwerse, J.G.1
Wiegant, J.2
Raap, A.K.3
Breuning, M.H.4
Van Ommen, G.J.B.5
-
38
-
-
0026454451
-
Involvement of a homolog of Drosophila trithorax by 11q23 chromosomal translocations in acute leukemias
-
Tkachuk DC, Kohler S and Cleary ML: Involvement of a homolog of Drosophila trithorax by 11q23 chromosomal translocations in acute leukemias. Cell 71: 691-700, 1992.
-
(1992)
Cell
, vol.71
, pp. 691-700
-
-
Tkachuk, D.C.1
Kohler, S.2
Cleary, M.L.3
-
39
-
-
0028908542
-
Interphase cytogenetics of the t 8;21 (q22;q22) associated with acute mylogenous leukemia by two-color fluorescence in situ hybridisation
-
Sacchi N, Magnani I, Kearney L, Wijsman J, Hagemeijer A and Darfler M: Interphase cytogenetics of the t 8;21) (q22;q22) associated with acute mylogenous leukemia by two-color fluorescence in situ hybridisation. Cancer Genet Cytogenet 79: 97-103, 1995.
-
(1995)
Cancer Genet Cytogenet
, vol.79
, pp. 97-103
-
-
Sacchi, N.1
Magnani, I.2
Kearney, L.3
Wijsman, J.4
Hagemeijer, A.5
Darfler, M.6
-
40
-
-
0031745208
-
Molecular cytogenetic delineation of the critical deleted region in the 5q- Syndrome
-
Jaju RJ, Boultwood J, Oliver FJ, Kostrzewa M, Fidler C, Parker N, McPherson JD, Morris SW, Wainscoat JS and Kearney L: Molecular cytogenetic delineation of the critical deleted region in the 5q- syndrome. Genes Chrom Cancer 22: 251-256, 1998.
-
(1998)
Genes Chrom Cancer
, vol.22
, pp. 251-256
-
-
Jaju, R.J.1
Boultwood, J.2
Oliver, F.J.3
Kostrzewa, M.4
Fidler, C.5
Parker, N.6
McPherson, J.D.7
Morris, S.W.8
Wainscoat, J.S.9
Kearney, L.10
-
41
-
-
0030960829
-
Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres
-
Knight SJL, Horsley SW, Regan R, Lawrie M, Maher EJ, Cardy DLN, Flint J and Kearney L: Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres. Eur J Hum Genet 5: 1-8, 1997.
-
(1997)
Eur J Hum Genet
, vol.5
, pp. 1-8
-
-
Knight, S.J.L.1
Horsley, S.W.2
Regan, R.3
Lawrie, M.4
Maher, E.J.5
Cardy, D.L.N.6
Flint, J.7
Kearney, L.8
-
42
-
-
0029912473
-
Karyotyping human chromosomes by combinatorial multi-fluor FISH
-
Speicher MR, Ballard SG and Ward DC: Karyotyping human chromosomes by combinatorial multi-fluor FISH. Nat Genet 12: 368-375, 1996.
-
(1996)
Nat Genet
, vol.12
, pp. 368-375
-
-
Speicher, M.R.1
Ballard, S.G.2
Ward, D.C.3
-
43
-
-
0038214755
-
Multicolor spectral karyotyping of human chromosomes
-
Schröck E, du Manoir S, Veldman T, Schoell B, Wienberg J, Ferguson-Smith MA, Ning Y, Ledbetter DH, Bar-Am I, Soenksen D, Garini Y and Ried T: Multicolor spectral karyotyping of human chromosomes. Science 273: 494-497, 1996.
-
(1996)
Science
, vol.273
, pp. 494-497
-
-
Schröck, E.1
Du Manoir, S.2
Veldman, T.3
Schoell, B.4
Wienberg, J.5
Ferguson-Smith, M.A.6
Ning, Y.7
Ledbetter, D.H.8
Bar-Am, I.9
Soenksen, D.10
Garini, Y.11
Ried, T.12
-
44
-
-
0026495364
-
Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
-
Kallionemi A, Kallionemi OP, Sudar D, Rutovitz D, Gray JW, Waldman F and Pinkel D: Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science 258: 818-821, 1992.
-
(1992)
Science
, vol.258
, pp. 818-821
-
-
Kallionemi, A.1
Kallionemi, O.P.2
Sudar, D.3
Rutovitz, D.4
Gray, J.W.5
Waldman, F.6
Pinkel, D.7
-
45
-
-
0031939328
-
Minimal sizes of deletions detected by comparative genomic hybridization
-
Bentz M, Plesch A, Stilgenbauer S, Döhner H and Lichter P: Minimal sizes of deletions detected by comparative genomic hybridization. Genes Chrom Cancer 21: 172-175, 1998.
-
(1998)
Genes Chrom Cancer
, vol.21
, pp. 172-175
-
-
Bentz, M.1
Plesch, A.2
Stilgenbauer, S.3
Döhner, H.4
Lichter, P.5
-
46
-
-
0030763177
-
Genome screening by comparative genomic hybridization
-
Forozan F, Karhu R, Kononen J, Kallioniemi A and Kallioniemi OP: Genome screening by comparative genomic hybridization. Trends Genet 13: 405-409, 1997.
-
(1997)
Trends Genet
, vol.13
, pp. 405-409
-
-
Forozan, F.1
Karhu, R.2
Kononen, J.3
Kallioniemi, A.4
Kallioniemi, O.P.5
-
47
-
-
0028900538
-
Comparative genomic hybridization in the investigation of myeloid leukemias
-
Bentz M, Döhner H, Huck K, Schütz B, Ganser A, Joos S, du Manior S and Lichter P: Comparative genomic hybridization in the investigation of myeloid leukemias. Genes Chrom Cancer 12: 193-200, 1995a.
-
(1995)
Genes Chrom Cancer
, vol.12
, pp. 193-200
-
-
Bentz, M.1
Döhner, H.2
Huck, K.3
Schütz, B.4
Ganser, A.5
Joos, S.6
Du Manior, S.7
Lichter, P.8
-
48
-
-
0029079152
-
Comparative genomic hybridization in chronic B-cell leukemias shows a high incidence of chromosomal gains and losses
-
Bentz M, Huck K, du Manoir S, Joos S, Werner CA, Fischer K, Döhner H and Lichter P: Comparative genomic hybridization in chronic B-cell leukemias shows a high incidence of chromosomal gains and losses. Blood 85: 3610-3618, 1995b.
-
(1995)
Blood
, vol.85
, pp. 3610-3618
-
-
Bentz, M.1
Huck, K.2
Du Manoir, S.3
Joos, S.4
Werner, C.A.5
Fischer, K.6
Döhner, H.7
Lichter, P.8
-
49
-
-
0030041048
-
Primary mediastinal (thymic) B-cell lymphoma is characterized by gains of chromosomal material including 9p and amplification of the REL gene
-
Joos S, Otãno-Joos MI, Ziegler S, Brüderlein S, du Manior S, Bentz M, Möller P and Lichter P: Primary mediastinal (thymic) B-cell lymphoma is characterized by gains of chromosomal material including 9p and amplification of the REL gene. Blood 87: 1571-1578, 1996.
-
(1996)
Blood
, vol.87
, pp. 1571-1578
-
-
Joos, S.1
Otãno-Joos, M.I.2
Ziegler, S.3
Brüderlein, S.4
Du Manior, S.5
Bentz, M.6
Möller, P.7
Lichter, P.8
-
50
-
-
0029904295
-
DNA copy number changes in diffuse large B-cell lymphoma: Comparative genomic hybridization study
-
Monni O, Joensuu H, Franssila K and Knuutila S: DNA copy number changes in diffuse large B-cell lymphoma: comparative genomic hybridization study. Blood 87: 5269-5278, 1996.
-
(1996)
Blood
, vol.87
, pp. 5269-5278
-
-
Monni, O.1
Joensuu, H.2
Franssila, K.3
Knuutila, S.4
-
51
-
-
0030795838
-
Chromosomal breakpoints and changes in DNA copy number in refractory acute myeloid leukemia
-
El-Rifai W, Elonen E, Larramendy M, Ruutu T and Knuutila S: Chromosomal breakpoints and changes in DNA copy number in refractory acute myeloid leukemia. Leukemia 11: 958-963, 1997.
-
(1997)
Leukemia
, vol.11
, pp. 958-963
-
-
El-Rifai, W.1
Elonen, E.2
Larramendy, M.3
Ruutu, T.4
Knuutila, S.5
-
52
-
-
0030701970
-
Matrix-based comparative genomic hybridization: Biochips to screen for genomic imbalances
-
Solinas-Toldo S, Lampel S, Stilgenbauer S, Nickolenko J, Benner A, Dohner H, Cremer T and Lichter P: Matrix-based comparative genomic hybridization: biochips to screen for genomic imbalances. Genes Chrom Cancer 20: 399-407, 1997.
-
(1997)
Genes Chrom Cancer
, vol.20
, pp. 399-407
-
-
Solinas-Toldo, S.1
Lampel, S.2
Stilgenbauer, S.3
Nickolenko, J.4
Benner, A.5
Dohner, H.6
Cremer, T.7
Lichter, P.8
-
53
-
-
0035179871
-
Assembly of microarrays for genome-wide measurement of DNA copy number
-
Snijders AM, Nowak N, Segraves, R, Blackwood S, Brown N, Conroy J, Hamilton G, Hindle AK, Huey B and Kimura K et al: Assembly of microarrays for genome-wide measurement of DNA copy number. Nat Genet 29: 263-264, 2001.
-
(2001)
Nat Genet
, vol.29
, pp. 263-264
-
-
Snijders, A.M.1
Nowak, N.2
Segraves, R.3
Blackwood, S.4
Brown, N.5
Conroy, J.6
Hamilton, G.7
Hindle, A.K.8
Huey, B.9
Kimura, K.10
-
54
-
-
10744221541
-
Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions
-
Yu W, Ballif BC, Kashork CD, Heilstedt HA, Howard LA, Cai WW, White LD, Liu W, Beaudet AL, Bejjani BA et al: Development of a comparative genomic hybridization microarray and demonstration of its utility with 25 well-characterized 1p36 deletions. Hum Mol Genet 12: 2145-2152, 2003.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 2145-2152
-
-
Yu, W.1
Ballif, B.C.2
Kashork, C.D.3
Heilstedt, H.A.4
Howard, L.A.5
Cai, W.W.6
White, L.D.7
Liu, W.8
Beaudet, A.L.9
Bejjani, B.A.10
-
55
-
-
2942575149
-
A cytogeneticist's perspective on genomic microarrays
-
Shaffer LG and Bejjani BA: A cytogeneticist's perspective on genomic microarrays. Hum Reprod Update 10(3): 221-226, 2004.
-
(2004)
Hum Reprod Update
, vol.10
, Issue.3
, pp. 221-226
-
-
Shaffer, L.G.1
Bejjani, B.A.2
-
56
-
-
0037422174
-
Hidden gene amplifications in aggressive B-cell non-Hodgkin lymphomas detected by microarray-based comparative genomic hybridization
-
Wessendorf S, Schwaenen C, Kohlhammer H, Kienle D, Wrobel G, Barth TF, Nessling M, Moller P, Dohner H and Lichter P et al: Hidden gene amplifications in aggressive B-cell non-Hodgkin lymphomas detected by microarray-based comparative genomic hybridization. Oncogene 22: 1425-1429, 2003.
-
(2003)
Oncogene
, vol.22
, pp. 1425-1429
-
-
Wessendorf, S.1
Schwaenen, C.2
Kohlhammer, H.3
Kienle, D.4
Wrobel, G.5
Barth, T.F.6
Nessling, M.7
Moller, P.8
Dohner, H.9
Lichter, P.10
|