-
1
-
-
17344366773
-
Establishment and characterization of a megakaryoblast cell line with amplication of MLL
-
ALLEN, R.J., SMITH, S.D., MOLDWIN, R.L., LU, M.M., GIORDANO, L., VIGNON, C., SUTO, Y., HARDEN, A., TOMEK, R., VELDMAN, T., REID, T., LARSON, R.A., LE BEAU, M.M., ROWLEY, J.D., and ZELEZNIK-LE, N. (1998). Establishment and characterization of a megakaryoblast cell line with amplication of MLL. Leukemia 12, 1119-1127.
-
(1998)
Leukemia
, vol.12
, pp. 1119-1127
-
-
Allen, R.J.1
Smith, S.D.2
Moldwin, R.L.3
Lu, M.M.4
Giordano, L.5
Vignon, C.6
Suto, Y.7
Harden, A.8
Tomek, R.9
Veldman, T.10
Reid, T.11
Larson, R.A.12
Le Beau, M.M.13
Rowley, J.D.14
Zeleznik-Le, N.15
-
2
-
-
0002425517
-
Subtelomeric rearrangements detected by FISH in patients with idiopathic mental retardation
-
ANDERLID, B., ANNERÉN, G., BLENNOW, E., and NORDENSKJOLD, M. (1999). Subtelomeric rearrangements detected by FISH in patients with idiopathic mental retardation. Am. J. Hum. Genet. 65 (Suppl.), A67.
-
(1999)
Am. J. Hum. Genet.
, vol.65
, Issue.SUPPL.
-
-
Anderlid, B.1
Annerén, G.2
Blennow, E.3
Nordenskjold, M.4
-
3
-
-
0011720930
-
Fluorescence in situ hybridization
-
S.L. Gersen and M.B. Keagle (eds.). Humana Press
-
BLANCATO, J.K. (1999). Fluorescence in situ hybridization. In The Principles of Clinical Cytogenetics. S.L. Gersen and M.B. Keagle (eds.). Humana Press, pp. 445-471.
-
(1999)
The Principles of Clinical Cytogenetics
, pp. 445-471
-
-
Blancato, J.K.1
-
4
-
-
1842415978
-
Previously hidden chromosome aberrations in t(12;15)-positive BALB/c plasmacytoma uncovered by multicolor spectral karyotyping
-
COLEMAN, A.E., SCHRÖCK, E., WEAVER, Z., DU MANOIR, S., YANG, F., FERGUSON-SMITH, M.A., RIED, T., and JANZ, S. (1997). Previously hidden chromosome aberrations in t(12;15)-positive BALB/c plasmacytoma uncovered by multicolor spectral karyotyping. Cancer Res. 57, 4585-4592.
-
(1997)
Cancer Res.
, vol.57
, pp. 4585-4592
-
-
Coleman, A.E.1
Schröck, E.2
Weaver, Z.3
Du Manoir, S.4
Yang, F.5
Ferguson-Smith, M.A.6
Ried, T.7
Janz, S.8
-
5
-
-
0023691590
-
Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes
-
CREMER, T., LICHTER, P., BORDEN, J., WARD, D.C., and MANUELIDIS, L. (1998). Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes. Hum. Genet. 80, 235-246.
-
(1998)
Hum. Genet.
, vol.80
, pp. 235-246
-
-
Cremer, T.1
Lichter, P.2
Borden, J.3
Ward, D.C.4
Manuelidis, L.5
-
6
-
-
0025120429
-
Mapping small DNA sequences by fluorescence in situ hybridization directly on banded metaphase chromosomes
-
FAN, Y.S., DAVIS, L.M., and SHOWS, T.B. (1990). Mapping small DNA sequences by fluorescence in situ hybridization directly on banded metaphase chromosomes. Proc. Natl. Acad. Sci. USA 87, 6223-6227.
-
(1990)
Proc. Natl. Acad. Sci. USA
, vol.87
, pp. 6223-6227
-
-
Fan, Y.S.1
Davis, L.M.2
Shows, T.B.3
-
7
-
-
0033001140
-
Complex rearrangement of chromosome 1, 7, and 16 in chronic myelocytic leukemia
-
FAN, Y.S., RIZKALLA, K., and BARR, R.M. (1999a). Complex rearrangement of chromosome 1, 7, and 16 in chronic myelocytic leukemia. Cancer Genet. Cytogenet. 112, 190-192.
-
(1999)
Cancer Genet. Cytogenet.
, vol.112
, pp. 190-192
-
-
Fan, Y.S.1
Rizkalla, K.2
Barr, R.M.3
-
8
-
-
0032828878
-
A new complex variant Philadelphia chromosome, t(1;9;22)ins(17;22), characterized by fluorescence in situ hybridization in an adult ALL
-
FAN, Y.S., RIZKALLA, K., and BARR, R.M. (1999b). A new complex variant Philadelphia chromosome, t(1;9;22)ins(17;22), characterized by fluorescence in situ hybridization in an adult ALL. Leukemia Res. 23, 1001-1006.
-
(1999)
Leukemia Res.
, vol.23
, pp. 1001-1006
-
-
Fan, Y.S.1
Rizkalla, K.2
Barr, R.M.3
-
9
-
-
0033543457
-
Small terminal deletion of 1p and duplication of 1q: Cytogenetics, FISH studies, and clinical observations at newborn and at age 16 years
-
FAN, Y.S., JUNG, J., and HAMILTON, B. (1999c). Small terminal deletion of 1p and duplication of 1q: cytogenetics, FISH studies, and clinical observations at newborn and at age 16 years. Am. J. Med. Genet. 86, 118-123.
-
(1999)
Am. J. Med. Genet.
, vol.86
, pp. 118-123
-
-
Fan, Y.S.1
Jung, J.2
Hamilton, B.3
-
10
-
-
0033555777
-
Increased karyotype precision using fluorescence in situ hybridization and spectral karyotyping in patients with myeloid malignancies
-
FLEISCHMAN, E.W., RESHMI, S., SOKOVA, O.I., KIRICHENKO, O.P., KONSTANTINOVA, L.N., KULAGINA, O.E., FRENKEL, M.A., and ROWLEY, J.D. (1999). Increased karyotype precision using fluorescence in situ hybridization and spectral karyotyping in patients with myeloid malignancies. Cancer Genet. Cytogenet. 108, 166-170.
-
(1999)
Cancer Genet. Cytogenet.
, vol.108
, pp. 166-170
-
-
Fleischman, E.W.1
Reshmi, S.2
Sokova, O.I.3
Kirichenko, O.P.4
Konstantinova, L.N.5
Kulagina, O.E.6
Frenkel, M.A.7
Rowley, J.D.8
-
11
-
-
0030511960
-
Spectral karyotyping
-
GARINI, Y., MACVILLE, M., DU MANOIR, S., BUCKWALD, R.A., LAVI, M., KATZIR N., WINE, D., BAR-AM, I., SCHRÖCK, E., CABIB, D., and RIED, T. (1996). Spectral karyotyping. Bioimaging 4, 65-72.
-
(1996)
Bioimaging
, vol.4
, pp. 65-72
-
-
Garini, Y.1
Macville, M.2
Du Manoir, S.3
Buckwald, R.A.4
Lavi, M.5
Katzir, N.6
Wine, D.7
Bar-Am, I.8
Schröck, E.9
Cabib, D.10
Ried, T.11
-
12
-
-
0027981573
-
Rapid generation of whole chromosome painting probes (WCPs) by chromosome microdissection
-
GUAN, X.Y., MELTZER, P., and TRENT, J. (1994). Rapid generation of whole chromosome painting probes (WCPs) by chromosome microdissection. Genomics 22, 101-107.
-
(1994)
Genomics
, vol.22
, pp. 101-107
-
-
Guan, X.Y.1
Meltzer, P.2
Trent, J.3
-
13
-
-
0031769001
-
Identification of de novo chromosomal markers and derivatives by spectral karyotyping
-
HADDAD, B.R., SCHRÖCK, E., MECK, J., COWAN J., YOUNG, H., FERGUSON-SMITH, M.A., DU MANOIR, S., and RIED, T. (1998). Identification of de novo chromosomal markers and derivatives by spectral karyotyping. Hum. Genet. 103, 619-625.
-
(1998)
Hum. Genet.
, vol.103
, pp. 619-625
-
-
Haddad, B.R.1
Schröck, E.2
Meck, J.3
Cowan, J.4
Young, H.5
Ferguson-Smith, M.A.6
Du Manoir, S.7
Ried, T.8
-
14
-
-
0031772122
-
Identification of an unusual marker chromosome by spectral karyotyping
-
HUANG, B., NING, Y., LAMB, A.N., SANDLIN, C.J., JAMEHDOR, M., RIED, T., and BARTLEY, J. (1998). Identification of an unusual marker chromosome by spectral karyotyping. Am. J. Med. Genet. 80, 368-372.
-
(1998)
Am. J. Med. Genet.
, vol.80
, pp. 368-372
-
-
Huang, B.1
Ning, Y.2
Lamb, A.N.3
Sandlin, C.J.4
Jamehdor, M.5
Ried, T.6
Bartley, J.7
-
15
-
-
0030960829
-
Development and clinical application of an innovative fluorescence in situ hybridization technique which detects submicroscopic rearrangements involving telomeres
-
KNIGHT S.J.L., HORSLEY, S.W., REGAN, R., LANVRIE, N.M., MAHER, E.J., CARDY, D.L.N., FLINT, J., and KEARNEY, L. (1997). 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)
Eur. J. Hum. Genet.
, vol.5
, pp. 1-8
-
-
Knight, S.J.L.1
Horsley, S.W.2
Regan, R.3
Lanvrie, N.M.4
Maher, E.J.5
Cardy, D.L.N.6
Flint, J.7
Kearney, L.8
-
16
-
-
0001745242
-
Molecular cytogenetics of continuous gene syndromes
-
C. Scriver, A. Beaudet, W. Sly, and D. Valle (eds.). McGraw Hill
-
LEDBETTER, D., and BALLABIO, A. (1995). Molecular cytogenetics of continuous gene syndromes. In The Metabolic Bases of Inherited Diseases, 7th ed. C. Scriver, A. Beaudet, W. Sly, and D. Valle (eds.). McGraw Hill, pp. 811-839.
-
(1995)
The Metabolic Bases of Inherited Diseases, 7th Ed.
, pp. 811-839
-
-
Ledbetter, D.1
Ballabio, A.2
-
17
-
-
1642642150
-
Comparative genomic hybridization arrays: Towards a "telomere chip"
-
LESE, C.M., ZHANG, X., PINKEL, D., BAO, P., LERMER, N., CHE, D., SHI, J., MÜLER, U., and LEDBETTER, D.H. (1999). Comparative genomic hybridization arrays: towards a "telomere chip." Am. J. Hum. Genet. 65 (Suppl.), A9.
-
(1999)
Am. J. Hum. Genet.
, vol.65
, Issue.SUPPL.
-
-
Lese, C.M.1
Zhang, X.2
Pinkel, D.3
Bao, P.4
Lermer, N.5
Che, D.6
Shi, J.7
Müler, U.8
Ledbetter, D.H.9
-
18
-
-
0032195407
-
Clinical applications of comparative genomic hybridization
-
LEVY, B., DUNN, T.M., KAFFE, S., KARDON, N., and HIRSCHHORN, K. (1998). Clinical applications of comparative genomic hybridization. Genet. Med. 1, 4-12.
-
(1998)
Genet. Med.
, vol.1
, pp. 4-12
-
-
Levy, B.1
Dunn, T.M.2
Kaffe, S.3
Kardon, N.4
Hirschhorn, K.5
-
19
-
-
16044371402
-
A complete set of human telomeric probes and their clinical application
-
NING, Y., ROSCHKE, A., SMITH, A.C.M., MACHA, M., PRECHT, K., REITHMAN, H., LEDBETTER, D., FLINT, J., HORSLEY, S., REGAN, R., KEARNEY, L., KNIGHT, S., KVALOY, K., and BROWN, W.R.A. (1996). A complete set of human telomeric probes and their clinical application. Nature Genet. 14, 86-89.
-
(1996)
Nature Genet.
, vol.14
, pp. 86-89
-
-
Ning, Y.1
Roschke, A.2
Smith, A.C.M.3
Macha, M.4
Precht, K.5
Reithman, H.6
Ledbetter, D.7
Flint, J.8
Horsley, S.9
Regan, R.10
Kearney, L.11
Knight, S.12
Kvaloy, K.13
Brown, W.R.A.14
-
20
-
-
0032934462
-
Molecular cytogenetic analysis of the bladder carcinoma cell line BK-10 by spectral karyotyping
-
PADILLA-NASH, H.M., NASH, W.G., PADILLA, G.M., ROBERSON, K.M., ROBERSON, C.N., MACVILLE, M., SCHROCK, E., and RIED, T. (1999). Molecular cytogenetic analysis of the bladder carcinoma cell line BK-10 by spectral karyotyping. Genes Chromosomes Cancer 25, 53-59.
-
(1999)
Genes Chromosomes Cancer
, vol.25
, pp. 53-59
-
-
Padilla-Nash, H.M.1
Nash, W.G.2
Padilla, G.M.3
Roberson, K.M.4
Roberson, C.N.5
Macville, M.6
Schrock, E.7
Ried, T.8
-
21
-
-
0031729663
-
FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14, and 16
-
PHELAN, M.C., BLACKBURN, W., ROGERS, R.C., CRAWFORD, E.C., COOLEY, N.R., JR., SCHRÖCK, E., NING, Y., and RIED, T. (1998). FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14, and 16. Prenat. Diagn. 18, 1174-1180.
-
(1998)
Prenat. Diagn.
, vol.18
, pp. 1174-1180
-
-
Phelan, M.C.1
Blackburn, W.2
Rogers, R.C.3
Crawford, E.C.4
Cooley Jr., N.R.5
Schröck, E.6
Ning, Y.7
Ried, T.8
-
22
-
-
0032170964
-
Multicolor spectral karyotyping identifies new recurring breakpoints and translocations in multiple myeloma
-
RAO, P.H., CIGUDOSA, J.C., NING, Y., CALASANZ, M.J., IIDA, S., TAGAWA, S., MICHAELI, J., KLEIN, B., DALLA-FAVERA, R., JHANWAR, S.C., RIED, T., and CHAGANTI, R.S.K. (1998). Multicolor spectral karyotyping identifies new recurring breakpoints and translocations in multiple myeloma. Blood 92, 1743-1748.
-
(1998)
Blood
, vol.92
, pp. 1743-1748
-
-
Rao, P.H.1
Cigudosa, J.C.2
Ning, Y.3
Calasanz, M.J.4
Iida, S.5
Tagawa, S.6
Michaeli, J.7
Klein, B.8
Dalla-Favera, R.9
Jhanwar, S.C.10
Ried, T.11
Chaganti, R.S.K.12
-
23
-
-
0033590672
-
De novo mosaic add(3) characterized to be trisomy 14q31-qter using spectral karyotyping and subtelomeric probes
-
REDDY, K.S., SULCOVA, V., YOUNG, H., BLANCATO, J.K., and HADDAD, B.R. (1999). De novo mosaic add(3) characterized to be trisomy 14q31-qter using spectral karyotyping and subtelomeric probes. Am. J. Med. Genet. 82, 318-321.
-
(1999)
Am. J. Med. Genet.
, vol.82
, pp. 318-321
-
-
Reddy, K.S.1
Sulcova, V.2
Young, H.3
Blancato, J.K.4
Haddad, B.R.5
-
24
-
-
0032920835
-
Hemangioendothelioma of bone in a patient with a constitutional supernumerary marker
-
ROGATTA, S.R., RAINHO, C.A., ZHANG, Z.M., FIGUEIREDO, F., BARBIERI-NETO, J., GEORGETTO, S.M., and SQUIRE, J.A. (1999). Hemangioendothelioma of bone in a patient with a constitutional supernumerary marker. Cancer Genet. Cytogenet. 110, 23-27.
-
(1999)
Cancer Genet. Cytogenet.
, vol.110
, pp. 23-27
-
-
Rogatta, S.R.1
Rainho, C.A.2
Zhang, Z.M.3
Figueiredo, F.4
Barbieri-Neto, J.5
Georgetto, S.M.6
Squire, J.A.7
-
25
-
-
0033559758
-
Spectral karyotype analysis of T-cell acute leukemia
-
ROWLEY, J.D., RESHMI, S., CARLSON, K., and ROULSTON, D. (1999). Spectral karyotype analysis of T-cell acute leukemia. Blood 93, 2038-2042.
-
(1999)
Blood
, vol.93
, pp. 2038-2042
-
-
Rowley, J.D.1
Reshmi, S.2
Carlson, K.3
Roulston, D.4
-
26
-
-
0032402134
-
Identification of new nonrandom translocations in multiple myeloma with multicolor spectral karyotyping
-
SAWYER, J.R., LUKACS, J.L., MUNSHI, N., DESIKAN, K.R., SINGHAL, S., MEHTA, J., SIEGEL, D., SHAUGHNESSY, J., and BARLOGIE, B. (1998). Identification of new nonrandom translocations in multiple myeloma with multicolor spectral karyotyping. Blood 92, 4269-4278.
-
(1998)
Blood
, vol.92
, pp. 4269-4278
-
-
Sawyer, J.R.1
Lukacs, J.L.2
Munshi, N.3
Desikan, K.R.4
Singhal, S.5
Mehta, J.6
Siegel, D.7
Shaughnessy, J.8
Barlogie, B.9
-
27
-
-
0038214755
-
Multicolor spectral karyotyping of human chromosomes
-
SCHRÖCK, E., DU MANOIR, S., VELDMAN, T., SCHOELL, B., WIENBERG, J., FERGUSON-SMITH, M.A., NING, Y., LEDBETTER, D.H., BAR-AM, I., SOENKSEN, D., GARINI, Y., and REID, T. (1996). Multicolor spectral karyotyping of human chromosomes. Science 273, 494-497.
-
(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
Reid, T.12
-
28
-
-
2642683176
-
Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities abnormalities
-
SCHRÖCK, E., VELDMAN, T., PADILLA-NASH, H., NING, Y., SPURBECK, J., JALAL, S., SHAFFER, L.G., PAPENHAUSEN, P., KOZMA, C., PHELAN, M.C., KJELDSEN, E., SCHONBERG, S.A., O'BRIEN, P., BIESECKER, L., DU MANOIR, S., and RIED, T. (1997). Spectral karyotyping refines cytogenetic diagnostics of constitutional chromosomal abnormalities abnormalities. Hum. Genet. 101, 255-262.
-
(1997)
Hum. Genet.
, vol.101
, pp. 255-262
-
-
Schröck, E.1
Veldman, T.2
Padilla-Nash, H.3
Ning, Y.4
Spurbeck, J.5
Jalal, S.6
Shaffer, L.G.7
Papenhausen, P.8
Kozma, C.9
Phelan, M.C.10
Kjeldsen, E.11
Schonberg, S.A.12
O'Brien, P.13
Biesecker, L.14
Du Manoir, S.15
Ried, T.16
-
29
-
-
0033031587
-
Coexistence of several unbalanced translocations in a case of neuroblastoma: The contribution of multicolor spectral karyotyping
-
TRAKHTENBROT, L., COHEN, N., ROSNER, E., GIPSH, N., BROK-SIMONI, F., MANDEL, M., AMARIGLIO, N., and RECHAVI, G. (1999). Coexistence of several unbalanced translocations in a case of neuroblastoma: the contribution of multicolor spectral karyotyping. Cancer Genet. Cytogenet. 112, 119-123.
-
(1999)
Cancer Genet. Cytogenet.
, vol.112
, pp. 119-123
-
-
Trakhtenbrot, L.1
Cohen, N.2
Rosner, E.3
Gipsh, N.4
Brok-Simoni, F.5
Mandel, M.6
Amariglio, N.7
Rechavi, G.8
-
30
-
-
0030909689
-
Hidden chromosome abnormalities in haematological malignancies detected by multicolor spectral karyotyping
-
VELDMAN, T., VIGNON, C., SCHRÖCK, E., ROWLEY, J.D., and RIED, T. (1997). Hidden chromosome abnormalities in haematological malignancies detected by multicolor spectral karyotyping. Nature Genet. 15, 406-410.
-
(1997)
Nature Genet.
, vol.15
, pp. 406-410
-
-
Veldman, T.1
Vignon, C.2
Schröck, E.3
Rowley, J.D.4
Ried, T.5
-
31
-
-
0032401944
-
Hidden chromosome abnormalities in a primary central nervous system lymphoma detected by multicolor spectral karyotyping
-
ZATTARA-CANNONI, H., DUFOUR, H., LEPIDI, H., CHATEL, C., GRISOLI, F., and VAGNER-CAPODANO, A.M. (1998). Hidden chromosome abnormalities in a primary central nervous system lymphoma detected by multicolor spectral karyotyping. Cancer Genet. Cytogenet. 107, 98-101.
-
(1998)
Cancer Genet. Cytogenet.
, vol.107
, pp. 98-101
-
-
Zattara-Cannoni, H.1
Dufour, H.2
Lepidi, H.3
Chatel, C.4
Grisoli, F.5
Vagner-Capodano, A.M.6
|