-
2
-
-
0025581552
-
Jauch A, Cremer T, Ward DC, Detection of Down syndrome by in situ hybridization with chromosome 21 specific DNA probes. In: Molecular genetics of chromosome 21 and Down syndrome (ed D Patterson) 69-78
-
Lichter P, Jauch A, Cremer T, Ward DC, Detection of Down syndrome by in situ hybridization with chromosome 21 specific DNA probes. In: Molecular genetics of chromosome 21 and Down syndrome (ed D Patterson) 69-78. Alan R Liss, New York, 1990.
-
(1990)
Alan R Liss, New York
-
-
Lichter, P.1
-
3
-
-
0021351337
-
Gosden JR, Chandley AC, Estimation of aneuploidy levels in human spermatozoa using chromosome specific probes and in situ hybridization
-
Joseph AM, Gosden JR, Chandley AC, Estimation of aneuploidy levels in human spermatozoa using chromosome specific probes and in situ hybridization. Hum Genet (1984) 66: 234-8.
-
(1984)
Hum Genet
, vol.66
, pp. 234-238
-
-
Joseph, A.M.1
-
4
-
-
0022916663
-
Landegent J, Bruckner a et al, Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: Diagnosis of trisomy 18 with probe LI.84
-
Cremer T, Landegent J, Bruckner A et al, Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe LI.84. Hum Genet (1986) 74: 346-52.
-
(1986)
Hum Genet
, vol.74
, pp. 346-352
-
-
Cremer, T.1
-
5
-
-
0029912473
-
Ballard SG, Ward DC, Karyotyping human chromosomes by combinatorial multi-fluor FISH
-
Speicher MR, Ballard SG, Ward DC, Karyotyping human chromosomes by combinatorial multi-fluor FISH. Nature Genet (1995) 12: 368-75.
-
(1995)
Nature Genet
, vol.12
, pp. 368-375
-
-
Speicher, M.R.1
-
6
-
-
0038214755
-
Du Manoir S, Veldman T et al, Multicolor spectral karyotyping of human chromosomes
-
Schröck E, du Manoir S, Veldman T et al, Multicolor spectral karyotyping of human chromosomes. Science (1996) 273: 494-7.
-
(1996)
Science
, vol.273
, pp. 494-497
-
-
Schröck, E.1
-
7
-
-
0026495364
-
Kallioniemi O-P, Sudar D et al, Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors
-
Kallioniemi A, Kallioniemi O-P, Sudar D et al, Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors. Science (1992) 258:818-21.
-
(1992)
Science
, vol.258
, pp. 818-821
-
-
Kallioniemi, A.1
-
8
-
-
0027447797
-
Scherthan H, Speicher MR et al, Detection of amplified genomic sequences by reverse chromosome painting using genomic tumor DNA as probe
-
Joos S, Scherthan H, Speicher MR et al, Detection of amplified genomic sequences by reverse chromosome painting using genomic tumor DNA as probe. Hum Genet (1993) 90: 584-9.
-
(1993)
Hum Genet
, vol.90
, pp. 584-589
-
-
Joos, S.1
-
9
-
-
0027537408
-
Speicher MR, Joos S et al. Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization
-
Du Manoir S, Speicher MR, Joos S et al. Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization. Hum Genet (1993) 90: 590-610.
-
(1993)
Hum Genet
, vol.90
, pp. 590-610
-
-
Du Manoir, S.1
-
10
-
-
0027966172
-
Kallioniemi A, Piper J et al, Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors
-
Kallioniemi O-P, Kallioniemi A, Piper J et al, Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumors. Genes Chromosom Cancer (1994) 10: 231-43.
-
(1994)
Genes Chromosom Cancer
, vol.10
, pp. 231-243
-
-
Kallioniemi, O.-P.1
-
11
-
-
0028934697
-
Schröck E, Bentz M et al, Quantitative analysis of comparative genomic hybridization
-
Du Manoir S, Schröck E, Bentz M et al, Quantitative analysis of comparative genomic hybridization. Cytometry (1995) 19: 27-41.
-
(1995)
Cytometry
, vol.19
, pp. 27-41
-
-
Du Manoir, S.1
-
12
-
-
33748136962
-
Bentz M, du Manoir S, Joos S, Comparative genomic hybridization. In: Human chromosomes (ed RS Verma, a Babu) 191-210
-
Lichter P, Bentz M, du Manoir S, Joos S, Comparative genomic hybridization. In: Human chromosomes (ed RS Verma, A Babu) 191-210. McGraw-Hill, New York, 1995.
-
(1995)
McGraw-Hill, New York
-
-
Lichter, P.1
-
13
-
-
0028907211
-
Rutovitz D, Sudar D et al, Computer image analysis of comparative genomic hybridization
-
Piper J, Rutovitz D, Sudar D et al, Computer image analysis of comparative genomic hybridization. Cytometry (1995) 19: 10-26.
-
(1995)
Cytometry
, vol.19
, pp. 10-26
-
-
Piper, J.1
-
14
-
-
0027376691
-
Du Manoir S, Schröck e et al, Molecular cytogenetic analysis of formalin-fixed, paraffin-embedded solid tumors by comparative genomic hybridization after universal DNA-amplification
-
Speicher MR, du Manoir S, Schröck E et al, Molecular cytogenetic analysis of formalin-fixed, paraffin-embedded solid tumors by comparative genomic hybridization after universal DNA-amplification. Hum Mol Genet (1993) 2: 1907-14.
-
(1993)
Hum Mol Genet
, vol.2
, pp. 1907-1914
-
-
Speicher, M.R.1
-
15
-
-
0029003468
-
Jauch A, Walt H et al, Correlation of microscopic phenotype with genotype in a formalinfixed, paraffin-embedded testicular germ cell tumor with universal DNA amplification, comparative genomic hybridization, and interphase cytogenetics
-
Speicher MR, Jauch A, Walt H et al, Correlation of microscopic phenotype with genotype in a formalinfixed, paraffin-embedded testicular germ cell tumor with universal DNA amplification, comparative genomic hybridization, and interphase cytogenetics. Am J Pathol (1995) 146: 1332-40.
-
(1995)
Am J Pathol
, vol.146
, pp. 1332-1340
-
-
Speicher, M.R.1
-
16
-
-
0029900741
-
Scheurlen W, Krauss J et al, Mapping of chromosomal gains and losses in primitive neuroectodermal tumors by comparative genomic hybridization
-
Schütz BR, Scheurlen W, Krauss J et al, Mapping of chromosomal gains and losses in primitive neuroectodermal tumors by comparative genomic hybridization. Genes Chromosom Cancer (1996) 16:196-203.
-
(1996)
Genes Chromosom Cancer
, vol.16
, pp. 196-203
-
-
Schütz, B.R.1
-
17
-
-
84909874848
-
Fischer K, Cabot GP et al, Incidence and prognostic significance of recurring chromosome abnormalities in chronic B-cell leukemias: An interphase cytogenetic analysis
-
Döhner H, Fischer K, Cabot GP et al, Incidence and prognostic significance of recurring chromosome abnormalities in chronic B-cell leukemias: an interphase cytogenetic analysis. Blood (1993) 83(Suppl 1): 2236.
-
(1993)
Blood
, vol.83
, Issue.SUPPL. 1
, pp. 2236
-
-
Döhner, H.1
-
18
-
-
0027457275
-
Döhner H, Bulgay-Mörschel M et al, High frequency of monoallelic retinoblastoma gene deletion in B-cell chronic lymphoid leukemia shown by interphase cytogenetics
-
Stilgenbauer S, Döhner H, Bulgay-Mörschel M et al, High frequency of monoallelic retinoblastoma gene deletion in B-cell chronic lymphoid leukemia shown by interphase cytogenetics. Blood (1993) 81:2118-24.
-
(1993)
Blood
, vol.81
, pp. 2118-2124
-
-
Stilgenbauer, S.1
-
19
-
-
0028589109
-
Pilz T, Fischer K et al, Molecular cytogenetic analysis of RB-1 deletions in chronic B-cell leukemias
-
Donner H, Pilz T, Fischer K et al, Molecular cytogenetic analysis of RB-1 deletions in chronic B-cell leukemias. Lenk Lymphoma (1994) 16: 97-103.
-
(1994)
Lenk Lymphoma
, vol.16
, pp. 97-103
-
-
Donner, H.1
-
20
-
-
0028987180
-
Fischer K, Bentz M et al, 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 et al, p53 gene deletion predicts for poor survival and non-response to therapy with purine analogs in chronic B-cell leukemias. Blood (1995) 85: 1580-9.
-
(1995)
Blood
, vol.85
, pp. 1580-1589
-
-
Döhner, H.1
-
21
-
-
0028824718
-
Mathieu U, Dreyling MH et al, CDKN2 gene deletion is not found in chronic lymphoid leukemias of B- And T-cell origin but is frequent in acute lymphoblastic leukemia
-
Schröder M, Mathieu U, Dreyling MH et al, CDKN2 gene deletion is not found in chronic lymphoid leukemias of B- and T-cell origin but is frequent in acute lymphoblastic leukemia. Br J Haematol (1995) 91: 865-70.
-
(1995)
Br J Haematol
, vol.91
, pp. 865-870
-
-
Schröder, M.1
-
22
-
-
0029099360
-
Leupolt E, Ohl S et al, Heterogeneity of deletions involving RB-1 and the D13S25 locus in B-cell chronic lymphocytic leukemia revealed by FISH
-
Stilgenbauer S, Leupolt E, Ohl S et al, Heterogeneity of deletions involving RB-1 and the D13S25 locus in B-cell chronic lymphocytic leukemia revealed by FISH. Cancer Res (1995) 55: 3475-7.
-
(1995)
Cancer Res
, vol.55
, pp. 3475-3477
-
-
Stilgenbauer, S.1
-
23
-
-
0029969111
-
Liebisch P, James MR et al, Molecular cytogenetic delineation of a novel critical genomic region in chromosome bands 1 Iq22.3-q23.1 in lymphoproliferative disorders
-
Stilgenbauer S, Liebisch P, James MR et al, Molecular cytogenetic delineation of a novel critical genomic region in chromosome bands 1 Iq22.3-q23.1 in lymphoproliferative disorders. Proc NatlAcad Sei USA (1996) in press.
-
(1996)
Proc NatlAcad Sei USA
-
-
Stilgenbauer, S.1
-
24
-
-
0025815704
-
Wessman M, Tiainen M et al, Trisomy 12 in chronic lymphocytic leukemia: An interphase cytogenetic study
-
Perez Losada A, Wessman M, Tiainen M et al, Trisomy 12 in chronic lymphocytic leukemia: an interphase cytogenetic study. Blood (1991) 78:775-81.
-
(1991)
Blood
, vol.78
, pp. 775-781
-
-
Perez Losada, A.1
-
25
-
-
0026533307
-
Le Beau MM, Vardiman JW et al, 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 et al, Detection of trisomy 12 in chronic lymphocytic leukemia by fluorescence in situ hybridization to interphase cells: a simple and sensitive method. Blood (1992) 79:1796-801.
-
(1992)
Blood
, vol.79
, pp. 1796-1801
-
-
Anastasi, J.1
-
26
-
-
0026680379
-
Wlodarska I, Sayed Aly M et al, Nonradioactive in situ hybridization for the detection and monitoring of trisomy 12 in B-cell chronic lymphocytic leukaemia
-
Cuneo A, Wlodarska I, Sayed Aly M et al, Nonradioactive in situ hybridization for the detection and monitoring of trisomy 12 in B-cell chronic lymphocytic leukaemia. Br J Haematol (1992) 81: 192-6.
-
(1992)
Br J Haematol
, vol.81
, pp. 192-196
-
-
Cuneo, A.1
-
27
-
-
0027288539
-
Pereira-Leahy JM, Drach JW et al, Fluorescent in situ hybridization and cytogenetic studies of trisomy 12 in chronic lymphocytic leukemia
-
Escudier SM, Pereira-Leahy JM, Drach JW et al, Fluorescent in situ hybridization and cytogenetic studies of trisomy 12 in chronic lymphocytic leukemia. Blood (1993) 81: 2702-7.
-
(1993)
Blood
, vol.81
, pp. 2702-2707
-
-
Escudier, S.M.1
-
28
-
-
0026539964
-
Kibbelaar RE, Kleiverda JK et al, Mosaicism of trisomy 12 in chronic lymphocytic leukemia detected by non-radioactive in situ hybridization
-
Raghoebier S, Kibbelaar RE, Kleiverda JK et al, Mosaicism of trisomy 12 in chronic lymphocytic leukemia detected by non-radioactive in situ hybridization. Leukemia (1993) 6:1220-6.
-
(1993)
Leukemia
, vol.6
, pp. 1220-1226
-
-
Raghoebier, S.1
-
29
-
-
0025019583
-
Le Beau MM, Vardiman JW, Westbrook CA, Detection of numerical chromosomal abnormalities in neoplastic hematopoietic cells by in situ hybridization with a chromosome-specific probe
-
Anastasi J, Le Beau MM, Vardiman JW, Westbrook CA, Detection of numerical chromosomal abnormalities in neoplastic hematopoietic cells by in situ hybridization with a chromosome-specific probe. Am J Pathol (1990) 136: 131-9.
-
(1990)
Am J Pathol
, vol.136
, pp. 131-139
-
-
Anastasi, J.1
-
30
-
-
0027310667
-
Pohl S, Bulgay-Mörschel M et al, Trisomy 12 in chronic lymphoid leukemias -a metaphase and interphase cytogenetic analysis
-
Döhner H, Pohl S, Bulgay-Mörschel M et al, Trisomy 12 in chronic lymphoid leukemias -a metaphase and interphase cytogenetic analysis. Leukemia (1993) 7: 516-20.
-
(1993)
Leukemia
, vol.7
, pp. 516-520
-
-
Döhner, H.1
-
31
-
-
0028299948
-
Cabot G, Moos M et al, Detection of chimeric BCR-ABL genes on bone marrow samples and blood smears in chronic myeloid and acute lymphoblastic leukemia by in situ hybridization
-
Bentz M, Cabot G, Moos M et al, Detection of chimeric BCR-ABL genes on bone marrow samples and blood smears in chronic myeloid and acute lymphoblastic leukemia by in situ hybridization. Blood (1994) 83: 1922-8.
-
(1994)
Blood
, vol.83
, pp. 1922-1928
-
-
Bentz, M.1
-
32
-
-
0029843439
-
Scholl C, Salat J et al, Design and validation of DNA probe sets for a comprehensive interphase analysis of acute myeloid leukemia
-
in press.
-
Fischer K, Scholl C, Salat J et al, Design and validation of DNA probe sets for a comprehensive interphase analysis of acute myeloid leukemia. Blood (1996) 88: in press.
-
(1996)
Blood
, vol.88
-
-
Fischer, K.1
-
33
-
-
0028848334
-
Bergerheim USR, Pan Y et al, Mapping of chromosomal gains and losses in prostate cancer by comparative genomic hybridization
-
Joos S, Bergerheim USR, Pan Y et al, Mapping of chromosomal gains and losses in prostate cancer by comparative genomic hybridization. Genes Chromosom Cancer (1995) 14:267-76.
-
(1995)
Genes Chromosom Cancer
, vol.14
, pp. 267-276
-
-
Joos, S.1
-
34
-
-
0029031775
-
Joos S, Vallinga M et al, Detection of chromosomal imbalances in bladder tumors by comparative genomic hybridization
-
Voorter C, Joos S, Vallinga M et al, Detection of chromosomal imbalances in bladder tumors by comparative genomic hybridization. Am J Pathol (1995) 146: 1341-54.
-
(1995)
Am J Pathol
, vol.146
, pp. 1341-1354
-
-
Voorter, C.1
-
35
-
-
0030478646
-
Bergerheim USR, Li C et al, Chromosomal imbalances in renal cell carcinoma and first cytogenetic data of familial cases analyzed by comparative genomic hybridization
-
Bentz M, Bergerheim USR, Li C et al, Chromosomal imbalances in renal cell carcinoma and first cytogenetic data of familial cases analyzed by comparative genomic hybridization. Cytogenet Cell Genet (1996) in press.
-
(1996)
Cytogenet Cell Genet
-
-
Bentz, M.1
-
36
-
-
0029761612
-
Wallrapp C, Muller-Pillasch F et al, Mapping of chromosomal imbalances in pancreatic carcinoma by comparative genomic hybridization
-
Solinas-Toldo S, Wallrapp C, Muller-Pillasch F et al, Mapping of chromosomal imbalances in pancreatic carcinoma by comparative genomic hybridization. Cancer Res (1996) 56: 3803-7.
-
(1996)
Cancer Res
, vol.56
, pp. 3803-3807
-
-
Solinas-Toldo, S.1
-
37
-
-
0028900538
-
Döhner H, Huck K et al, Comparative genomic hybridization in the investigation of myeloid leukemias
-
Bentz M, Döhner H, Huck K et al, Comparative genomic hybridization in the investigation of myeloid leukemias. Genes Chromosom Cancer (1995) 12: 193-200.
-
(1995)
Genes Chromosom Cancer
, vol.12
, pp. 193-200
-
-
Bentz, M.1
-
38
-
-
0029079152
-
Huck K, du Manoir S et al, Comparative genomic hybridization in chronic B-cell leukemias reveals additional chromosomal gains and losses
-
Bentz M, Huck K, du Manoir S et al, Comparative genomic hybridization in chronic B-cell leukemias reveals additional chromosomal gains and losses. Blood (1995) 85:3610-18.
-
(1995)
Blood
, vol.85
, pp. 3610-3618
-
-
Bentz, M.1
-
39
-
-
9444227674
-
Werner CA, Döhner H et al, High incidences of chromosomal imbalances and gene amplifications in the classical follicular variant of follicle center lymphoma
-
Bentz M, Werner CA, Döhner H et al, High incidences of chromosomal imbalances and gene amplifications in the classical follicular variant of follicle center lymphoma. Blood (1996) 88: 1437t4.
-
(1996)
Blood
, vol.88
, pp. 1437
-
-
Bentz, M.1
-
40
-
-
0030041048
-
Otano-Joos MI, Ziegler S et al, Primary mediastinal (thymic) B-cell lymphoma is characterized by gains of chromosomal material including 9p and of the REL gene
-
Joos S, Otano-Joos MI, Ziegler S et al, Primary mediastinal (thymic) B-cell lymphoma is characterized by gains of chromosomal material including 9p and of the REL gene. Blood (1996) 87: 1571-8.
-
(1996)
Blood
, vol.87
, pp. 1571-1578
-
-
Joos, S.1
-
41
-
-
0028143269
-
DeVries S, Chu L et al, Analysis of changes in DNA sequence copy number by comparative genomic hybridization in archival paraffin-embedded tumor samples
-
Isola J, DeVries S, Chu L et al, Analysis of changes in DNA sequence copy number by comparative genomic hybridization in archival paraffin-embedded tumor samples. Am J Pathol ( 1994) 145: 1301-8.
-
(1994)
Am J Pathol
, vol.145
, pp. 1301-1308
-
-
Isola, J.1
-
42
-
-
0028887369
-
Kallioniemi A-C, Syvänen A-C et al, Genedc changes in primary and recurrent prostate cancer by comparative genomic hybridization
-
Visakorpi T, Kallioniemi A-C, Syvänen A-C et al, Genedc changes in primary and recurrent prostate cancer by comparative genomic hybridization. Cancer Res (1995) 55: 342-7.
-
(1995)
Cancer Res
, vol.55
, pp. 342-347
-
-
Visakorpi, T.1
-
43
-
-
85176675347
-
Hyytinen E, Palmberg C et al, Analysis of genetic changes underlying local recurrence of prostate carcinoma during androgen deprivation therapy
-
Koivisto P, Hyytinen E, Palmberg C et al, Analysis of genetic changes underlying local recurrence of prostate carcinoma during androgen deprivation therapy. AmJPathol( 1995) 6: 1606-14.
-
(1995)
AmJPathol
, vol.6
, pp. 1606-1614
-
-
Koivisto, P.1
-
44
-
-
0030068216
-
Schröck E, du Manoir S et al, Gain of chromosome 3q defines the transition from severe dysplasia to invasive carcinoma of the uterine cervix
-
Heselmeyer K, Schröck E, du Manoir S et al, Gain of chromosome 3q defines the transition from severe dysplasia to invasive carcinoma of the uterine cervix. Proc Natl Acad Sei USA (1996) 93: 479-84.
-
(1996)
Proc Natl Acad Sei USA
, vol.93
, pp. 479-484
-
-
Heselmeyer, K.1
-
45
-
-
0029736825
-
Säbel M, Reifenberger J et al, Characterization of genomic alterations associated with glioma progression by comparative genomic hybridization
-
Weber R, Säbel M, Reifenberger J et al, Characterization of genomic alterations associated with glioma progression by comparative genomic hybridization. Oncogene (1996) in press.
-
(1996)
Oncogene
-
-
Weber, R.1
-
47
-
-
0028848339
-
Almeida A, Gerbault-Seureau M et al, Identification of amplified DNA sequences in breast cancer and their organization within homogeneously staining regions
-
Muleris M, Almeida A, Gerbault-Seureau M et al, Identification of amplified DNA sequences in breast cancer and their organization within homogeneously staining regions. Genes Chromosom Cancer (1995) 14: 155-63.
-
(1995)
Genes Chromosom Cancer
, vol.14
, pp. 155-163
-
-
Muleris, M.1
-
48
-
-
0028849283
-
Just KE, Holtgreve-Grez H et al, Comparative genomic hybridization of formalinfixed, paraffin-embedded breast tumors reveals different patterns of chromosomal gains and losses in fibroadenomas and aneuploid carcinomas
-
Ried T, Just KE, Holtgreve-Grez H et al, Comparative genomic hybridization of formalinfixed, paraffin-embedded breast tumors reveals different patterns of chromosomal gains and losses in fibroadenomas and aneuploid carcinomas. Cancer Res (1995) 55:5415-23.
-
(1995)
Cancer Res
, vol.55
, pp. 5415-5423
-
-
Ried, T.1
-
49
-
-
0028874583
-
Kallioniemi OP, Chu LAV et al, Genetic aberrations detected by comparative genomic hybridization predict outcome in node-negative breast cancer
-
Isola JJ, Kallioniemi OP, Chu LAV et al, Genetic aberrations detected by comparative genomic hybridization predict outcome in node-negative breast cancer. AmJPathol (1995) 147: 905-11.
-
(1995)
AmJPathol
, vol.147
, pp. 905-911
-
-
Isola, J.J.1
-
50
-
-
33748154959
-
Catalog of Chromosome Aberrations in Cancer (assoc eds Johansson B, Mertens F). 5th edn
-
Mitelman, Catalog of Chromosome Aberrations in Cancer (assoc eds Johansson B, Mertens F). 5th edn, Wiley-Liss, New York 1994.
-
(1994)
Wiley-Liss, New York
-
-
Mitelman1
|