-
3
-
-
0024336365
-
Biology of disease: Molecular mechanism of oncogenes
-
Seemayer TA, Cavenee WK: Biology of disease: Molecular mechanism of oncogenes. Lab Invest 60:585, 1989.
-
(1989)
Lab Invest
, vol.60
, pp. 585
-
-
Seemayer, T.A.1
Cavenee, W.K.2
-
4
-
-
0343319476
-
Fluorescence in situ hybridization with human chromosome-specific libraries: Detection of trisomy 21 and translocations of chromosome 4
-
Pinkel D, Landegent J, Collins C, Fuscoe J, Segraves R, Lucas J, Gray J: Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4. Proc Natl Acad Sci USA 85:9138, 1988.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 9138
-
-
Pinkel, D.1
Landegent, J.2
Collins, C.3
Fuscoe, J.4
Segraves, R.5
Lucas, J.6
Gray, J.7
-
5
-
-
1842346815
-
Detection of numeral and structural chromosome aberrations in interphase nuclei by fluorescence in situ hybridization
-
Raap AK, Arnoldus EPJ, Nederlof PM, Smith VTHBM, Cornelisse CJ, van der Ploeg M: Detection of numeral and structural chromosome aberrations in interphase nuclei by fluorescence in situ hybridization. Trans R Microsc Soc 1:661, 1990.
-
(1990)
Trans R Microsc Soc
, vol.1
, pp. 661
-
-
Raap, A.K.1
Arnoldus, E.P.J.2
Nederlof, P.M.3
Smith, V.T.H.B.M.4
Cornelisse, C.J.5
Van Der Ploeg, M.6
-
6
-
-
0025019583
-
Detection of numeral 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 numeral chromosomal abnormalities in neoplastic hematopoietic cells by in situ hybridization with a chromosome-specific probe. Am J Pathol 136:131, 1990.
-
(1990)
Am J Pathol
, vol.136
, pp. 131
-
-
Anastasi, J.1
Le Beau, M.M.2
Vardiman, J.W.3
Westbrook, C.A.4
-
7
-
-
0025811162
-
Detection of trisomy 8 in hematological disorders by in situ hybridization
-
Kibbelaar RE, van Kamp H, Dreef EJ, Wessels JW, Beverstock GC, Raap AK, Fibbe WE, den Ottolander GJ, Kluin PM: Detection of trisomy 8 in hematological disorders by in situ hybridization. Cytogenet Cell Genet 56:132, 1991.
-
(1991)
Cytogenet Cell Genet
, vol.56
, pp. 132
-
-
Kibbelaar, R.E.1
Van Kamp, H.2
Dreef, E.J.3
Wessels, J.W.4
Beverstock, G.C.5
Raap, A.K.6
Fibbe, W.E.7
Den Ottolander, G.J.8
Kluin, P.M.9
-
8
-
-
0026014194
-
Improved interpretation of complex chromosomal rearrangements by combined GTG banding and in situ suppression hybridization using chromosome-specific libraries and cosmid probes
-
Smit VT, Wessels JW, Mollevanger P, Dauwerse JG, van Vliet M, Beverstock GC, Breuning MH, Devilee P, Raap AK, Cornelisse CJ: Improved interpretation of complex chromosomal rearrangements by combined GTG banding and in situ suppression hybridization using chromosome-specific libraries and cosmid probes. Genes Chromosom Cancer 3:239, 1991.
-
(1991)
Genes Chromosom Cancer
, vol.3
, pp. 239
-
-
Smit, V.T.1
Wessels, J.W.2
Mollevanger, P.3
Dauwerse, J.G.4
Van Vliet, M.5
Beverstock, G.C.6
Breuning, M.H.7
Devilee, P.8
Raap, A.K.9
Cornelisse, C.J.10
-
9
-
-
0015246254
-
A rapid banding technique for human chromosomes
-
Seabright M: A rapid banding technique for human chromosomes. Lancet ii:971-972, 1971.
-
(1971)
Lancet
, vol.2
, pp. 971-972
-
-
Seabright, M.1
-
10
-
-
0024424331
-
Detection of chromosome aberrations in interphase tumor nuclei by nonradioactive in situ hybridization
-
Nederlof PM, van der Flier S, Raap AK, Tanke HJ, van der Ploeg M, Kornips F, Geraedts JP: Detection of chromosome aberrations in interphase tumor nuclei by nonradioactive in situ hybridization. Cancer Genet Cytogenet 42:87, 1989.
-
(1989)
Cancer Genet Cytogenet
, vol.42
, pp. 87
-
-
Nederlof, P.M.1
Van Der Flier, S.2
Raap, A.K.3
Tanke, H.J.4
Van Der Ploeg, M.5
Kornips, F.6
Geraedts, J.P.7
-
11
-
-
0025689326
-
Cytogenetic analysis of human solid tumors by in situ hybridization with a set of 12 chromosome-specific DNA probes
-
van Dekken H, Pizzolo JG, Reuter VE, Melamed MR: Cytogenetic analysis of human solid tumors by in situ hybridization with a set of 12 chromosome-specific DNA probes. Cytogenet Cell Genet 54:103, 1990.
-
(1990)
Cytogenet Cell Genet
, vol.54
, pp. 103
-
-
Van Dekken, H.1
Pizzolo, J.G.2
Reuter, V.E.3
Melamed, M.R.4
-
12
-
-
0026026980
-
Detection of monosomy in interphase nuclei and identification of marker chromosomes using biotinylated alpha-satellite DNA probes
-
Kiechle-Schwarz M, Decker HJH, Berger CS, Fiebig HH, Sandberg AA: Detection of monosomy in interphase nuclei and identification of marker chromosomes using biotinylated alpha-satellite DNA probes. Cancer Genet Cytogenet 51:23, 1991.
-
(1991)
Cancer Genet Cytogenet
, vol.51
, pp. 23
-
-
Kiechle-Schwarz, M.1
Decker, H.J.H.2
Berger, C.S.3
Fiebig, H.H.4
Sandberg, A.A.5
-
13
-
-
0023692635
-
Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries
-
Lichter P, Cremer T, Borden J, Manuelidis L, Ward DC: Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries. Human Genet 80:224, 1988.
-
(1988)
Human Genet
, vol.80
, pp. 224
-
-
Lichter, P.1
Cremer, T.2
Borden, J.3
Manuelidis, L.4
Ward, D.C.5
-
14
-
-
0026348682
-
Translocation(8;21) in acute nonlymphocytic leukemia delineated by chromosomal in situ suppression hybridization
-
Popp S, Jauch A, Qiu JY, Smialek B, Cremer T, Becher R: Translocation(8;21) in acute nonlymphocytic leukemia delineated by chromosomal in situ suppression hybridization. Cancer Genet Cytogenet 57: 103, 1991.
-
(1991)
Cancer Genet Cytogenet
, vol.57
, pp. 103
-
-
Popp, S.1
Jauch, A.2
Qiu, J.Y.3
Smialek, B.4
Cremer, T.5
Becher, R.6
-
15
-
-
0026350942
-
Use of fluorescent in situ hybridization for marker chromosome identification in congenital and neoplastic disorders
-
Schad CR, Kraker WJ, Jalal SM, Tallman MS, Londer HN, Cook LP, Jenkins RB: Use of fluorescent in situ hybridization for marker chromosome identification in congenital and neoplastic disorders. Am J Clin Pathol 96:203, 1991.
-
(1991)
Am J Clin Pathol
, vol.96
, pp. 203
-
-
Schad, C.R.1
Kraker, W.J.2
Jalal, S.M.3
Tallman, M.S.4
Londer, H.N.5
Cook, L.P.6
Jenkins, R.B.7
-
16
-
-
0028609788
-
Characterization of the CHOP breakpoints and fusion transcripts in myxoid liposarcomas with the 12:16 translocation
-
Panagopoulos I, Mandahl N, Ron D, Hoglund M, Nilbert M, Mertens F, Mitelman F, Aman P: Characterization of the CHOP breakpoints and fusion transcripts in myxoid liposarcomas with the 12:16 translocation. Cancer Res 54:6500, 1994.
-
(1994)
Cancer Res
, vol.54
, pp. 6500
-
-
Panagopoulos, I.1
Mandahl, N.2
Ron, D.3
Hoglund, M.4
Nilbert, M.5
Mertens, F.6
Mitelman, F.7
Aman, P.8
-
17
-
-
0028100890
-
Mapping of the 12q12-q22 region with respect to tumor translocation breakpoints
-
Pedeutour F, Merscher S, Durieux E, Montgomery K, Krauter K, Clevy JP, Barcelo G, Kecherlapati R, Gaudray P, Turc-Carel C: Mapping of the 12q12-q22 region with respect to tumor translocation breakpoints. Genomics 22:512, 1995.
-
(1995)
Genomics
, vol.22
, pp. 512
-
-
Pedeutour, F.1
Merscher, S.2
Durieux, E.3
Montgomery, K.4
Krauter, K.5
Clevy, J.P.6
Barcelo, G.7
Kecherlapati, R.8
Gaudray, P.9
Turc-Carel, C.10
-
18
-
-
0028924452
-
12q13, a new recurrent breakpoint in acute non-lymphoblastic leukemia
-
Seyger MM, Ritterbach J, Creutzig U, Gnekow AK, Gobel U, Graf N, Reiter A, Lampert F, Harbott J: 12q13, a new recurrent breakpoint in acute non-lymphoblastic leukemia. Cancer Genet Cytogenet 80:23, 1995.
-
(1995)
Cancer Genet Cytogenet
, vol.80
, pp. 23
-
-
Seyger, M.M.1
Ritterbach, J.2
Creutzig, U.3
Gnekow, A.K.4
Gobel, U.5
Graf, N.6
Reiter, A.7
Lampert, F.8
Harbott, J.9
-
19
-
-
0029150161
-
A unique chromosome translocation, t(11;12;18) (q13;q13;q12), in primary lung lymphoma
-
Kubonishi I, Sugito S, Kobayashi M, Asahi Y, Tsuchiya T, Yamashiro T, Miyoshi I: A unique chromosome translocation, t(11;12;18) (q13;q13;q12), in primary lung lymphoma. Cancer Genet Cytogenet 82:54, 1995.
-
(1995)
Cancer Genet Cytogenet
, vol.82
, pp. 54
-
-
Kubonishi, I.1
Sugito, S.2
Kobayashi, M.3
Asahi, Y.4
Tsuchiya, T.5
Yamashiro, T.6
Miyoshi, I.7
-
21
-
-
0026082114
-
Painting of defined chromosomal regions by in situ suppression hybridization of libraries from laser-microdissected chromosomes
-
Lengauer C, Eckelt A, Weith A, Endlich N, Ponelies N, Lichter P, Greulich KO, Cremer T: Painting of defined chromosomal regions by in situ suppression hybridization of libraries from laser-microdissected chromosomes. Cytogenet Cell Genet 56:27, 1991.
-
(1991)
Cytogenet Cell Genet
, vol.56
, pp. 27
-
-
Lengauer, C.1
Eckelt, A.2
Weith, A.3
Endlich, N.4
Ponelies, N.5
Lichter, P.6
Greulich, K.O.7
Cremer, T.8
-
22
-
-
0025120429
-
Mapping small DNA sequences by fluorescence in situ hybridization directly on banded metaphase chromosomes
-
Fan Y, Davis LM, Shows TB: Mapping small DNA sequences by fluorescence in situ hybridization directly on banded metaphase chromosomes. Proc Natl Acad Sci USA 87:6223, 1990.
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 6223
-
-
Fan, Y.1
Davis, L.M.2
Shows, T.B.3
-
23
-
-
0025216124
-
Microdissection of banded human chromosomes
-
Senger G, Luedecke HJ, Horsthemke B, Claussen U: Microdissection of banded human chromosomes. Human Genet 84:507, 1990.
-
(1990)
Human Genet
, vol.84
, pp. 507
-
-
Senger, G.1
Luedecke, H.J.2
Horsthemke, B.3
Claussen, U.4
-
24
-
-
0025237846
-
Construction and characterization of band-specific DNA libraries
-
Luedecke HJ, Senger G, Claussen U, Horsthemke B: Construction and characterization of band-specific DNA libraries. Human Genet 84:512, 1990.
-
(1990)
Human Genet
, vol.84
, pp. 512
-
-
Luedecke, H.J.1
Senger, G.2
Claussen, U.3
Horsthemke, B.4
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