-
1
-
-
0038214755
-
Multicolor Spectral Karyotyping of Human Chromosomes
-
Schroeck, E., Manoir, S., Veldman, T., et al., Multicolor Spectral Karyotyping of Human Chromosomes, Science, 1996, vol. 273, pp. 494-497.
-
(1996)
Science
, vol.273
, pp. 494-497
-
-
Schroeck, E.1
Manoir, S.2
Veldman, T.3
-
2
-
-
0029912473
-
Karyotyping Human Chromosomes by Combinatorial Multi-Fluor FISH
-
Speicher, M.R., Ballard, S.G., and Ward, D.C., Karyotyping Human Chromosomes by Combinatorial Multi-Fluor FISH, Nat. Genet., 1996, vol. 12, pp. 368-375.
-
(1996)
Nat. Genet.
, vol.12
, pp. 368-375
-
-
Speicher, M.R.1
Ballard, S.G.2
Ward, D.C.3
-
3
-
-
0031769001
-
Identification of de Novo Chromosomal Markers and Derivatives by Spectral Karyotyping
-
Haddad, B.R., Schroeck, E., Meek, J., et al., Identification of De Novo Chromosomal Markers and Derivatives by Spectral Karyotyping, Hum. Genet., 1998, vol. 103, pp. 619-625.
-
(1998)
Hum. Genet.
, vol.103
, pp. 619-625
-
-
Haddad, B.R.1
Schroeck, E.2
Meek, J.3
-
4
-
-
19244361886
-
Precise Localization of 3p25 Breakpoints in Four Patients with the 3p-Syndorme
-
Drumheller, T., McGillivray, B.C., Behrner, D., et al., Precise Localization of 3p25 Breakpoints in Four Patients with the 3p-Syndorme, J. Med. Genet., 1996, vol. 33, no. 10, pp. 842-847.
-
(1996)
J. Med. Genet.
, vol.33
, Issue.10
, pp. 842-847
-
-
Drumheller, T.1
McGillivray, B.C.2
Behrner, D.3
-
5
-
-
0347055299
-
FISH on Uncultured Amniocytes Is a Highly Reliable Screening Method for Aneuploidies
-
Goetze, A., MiBbach, D., Becl, C., et al., FISH on Uncultured Amniocytes Is a Highly Reliable Screening Method for Aneuploidies, Med. Genet., 2000, vol. 12, p. 63.
-
(2000)
Med. Genet.
, vol.12
, pp. 63
-
-
Goetze, A.1
MiBbach, D.2
Becl, C.3
-
6
-
-
0034064674
-
Chromosome Analysis of Blastomers from Human Embryos by Using Comparative Genomic Hybridization
-
Voullaire, L., Slater, H., Williamson, R., and Wilton, L., Chromosome Analysis of Blastomers from Human Embryos by Using Comparative Genomic Hybridization, Hum. Genet., 2000, vol. 106, pp. 210-217.
-
(2000)
Hum. Genet.
, vol.106
, pp. 210-217
-
-
Voullaire, L.1
Slater, H.2
Williamson, R.3
Wilton, L.4
-
7
-
-
0345793936
-
Peculiarities of Organization and Present State of Prenatal Diagnosis Service in Russia
-
Baranov, V.S., Peculiarities of Organization and Present State of Prenatal Diagnosis Service in Russia, E.C.A. News Lett., 1999, no. 3, pp. 9-10.
-
(1999)
E.C.A. News Lett.
, vol.3
, pp. 9-10
-
-
Baranov, V.S.1
-
8
-
-
0345793937
-
The Use of Multi-Fluor Fluorescence in Situ Hybridization (FISH) to Diagnose Chromosome Abnormalities
-
Moscow
-
Vorsanova, S.G., Yurov, Yu.B., Solov'ev, I.V., et al., The Use of Multi-Fluor Fluorescence In Situ Hybridization (FISH) to Diagnose Chromosome Abnormalities, Vos'maya itogovaya konferentsiya "Genom cheloveka-98" (8th Conf. "Human Genome-98"), Moscow, 1998, p. 70.
-
(1998)
Vos'maya Itogovaya Konferentsiya "Genom Cheloveka-98" (8th Conf. "Human Genome-98")
, pp. 70
-
-
Vorsanova, S.G.1
Yurov, Yu.B.2
Solov'ev, I.V.3
-
9
-
-
0031613689
-
Identification of Human Marker Chromosomes and Translocations with a Computer-Based Diagnostic Database and Fluorescence in Situ Hybridization
-
Moscow
-
Nazarenko, S.A., Ostroverkhova, N.V., Puzyrev, V.P., etal., Identification of Human Marker Chromosomes and Translocations with a Computer-Based Diagnostic Database and Fluorescence In Situ Hybridization, Genetika (Moscow), 1998, vol. 34, no. 1, pp. 114-122.
-
(1998)
Genetika
, vol.34
, Issue.1
, pp. 114-122
-
-
Nazarenko, S.A.1
Ostroverkhova, N.V.2
Puzyrev, V.P.3
-
10
-
-
0029874862
-
Interstitial Deletion of Chromosome 6q: Report of a Case and Precise Definition of the Breakpoints by Microdissection and Reverse Painting
-
Rubtsov, N., Senger, G., Kucera, H., et al., Interstitial Deletion of Chromosome 6q: Report of a Case and Precise Definition of the Breakpoints by Microdissection and Reverse Painting, Hum. Genet., 1996, vol. 97, pp. 705-709.
-
(1996)
Hum. Genet.
, vol.97
, pp. 705-709
-
-
Rubtsov, N.1
Senger, G.2
Kucera, H.3
-
11
-
-
0006719288
-
A New Simple Version of Chromosome Microdissection Tested by Probe Generation for 24-Multicolor FISH, Multicolor Banding (MCB), ZOO-FISH and in Clinical Diagnostics
-
Rubtsov, N., Karamysheva, T., Babochkina, T., et al., A New Simple Version of Chromosome Microdissection Tested by Probe Generation for 24-Multicolor FISH, Multicolor Banding (MCB), ZOO-FISH and in Clinical Diagnostics, Med. Genet., 2000, vol. 12, p. 65.
-
(2000)
Med. Genet.
, vol.12
, pp. 65
-
-
Rubtsov, N.1
Karamysheva, T.2
Babochkina, T.3
-
12
-
-
0035376611
-
Clinical and Molecular-Cytogenetic Analyses of a Rare Case of Mosaicism for Partial Monosomy 3p and Partial Trisomy 10q in Man
-
Moscow
-
Karamysheva, T.V., Matveeva, V.G., Shorina, A.R., and Rubtsov, N.B., Clinical and Molecular-Cytogenetic Analyses of a Rare Case of Mosaicism for Partial Monosomy 3p and Partial Trisomy 10q in Man, Genetika (Moscow), 2001, vol. 37, no. 6, pp. 811-816.
-
(2001)
Genetika
, vol.37
, Issue.6
, pp. 811-816
-
-
Karamysheva, T.V.1
Matveeva, V.G.2
Shorina, A.R.3
Rubtsov, N.B.4
-
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., et al., Delineation of Individual Human Chromosomes in Metaphase and Interphase Cells by In Situ Suppression Hybridization Using Recombinant DNA Libraries, Hum. Genet., 1988 vol. 80, pp. 224-234.
-
(1988)
Hum. Genet.
, vol.80
, pp. 224-234
-
-
Lichter, P.1
Cremer, T.2
Borden, J.3
-
16
-
-
0025007098
-
The Isochromosome 18p Syndrome: Conformation of Cytogenetic Diagnosis in Nine Cases by in Situ Hybridization
-
Callen, D.F., Freemantle, C.J., et al., The Isochromosome 18p Syndrome: Conformation of Cytogenetic Diagnosis in Nine Cases by In Situ Hybridization, Am. J. Hum. Genet., 1990, vol. 47, pp. 493-498.
-
(1990)
Am. J. Hum. Genet.
, vol.47
, pp. 493-498
-
-
Callen, D.F.1
Freemantle, C.J.2
-
17
-
-
0030999555
-
A Breakpoint Map of Recurrent Chromosomal Rearrangements in Human Neoplasia
-
Mitelman, F., Mertens, F., and Johansson, B., A Breakpoint Map of Recurrent Chromosomal Rearrangements in Human Neoplasia, Nat. Genet., 1997, pp. 415-474.
-
(1997)
Nat. Genet.
, pp. 415-474
-
-
Mitelman, F.1
Mertens, F.2
Johansson, B.3
-
18
-
-
0001805746
-
Cytogenetics in Myeloid Leukemia
-
Potter, A.M. and Watmore, A., Cytogenetics in Myeloid Leukemia, Human Cytogenetics: A Practical Approach, 1992, vol. 11, pp. 27-67.
-
(1992)
Human Cytogenetics: A Practical Approach
, vol.11
, pp. 27-67
-
-
Potter, A.M.1
Watmore, A.2
-
20
-
-
0347055298
-
Cytogenetic Diagnostics of Oncological Disease
-
Rubtsov, N.B. and Karamysheva, T.V., Cytogenetic Diagnostics of Oncological Disease, Klin. Onkol. Gematol., 2000, no. 2, pp. 7-21.
-
(2000)
Klin. Onkol. Gematol.
, Issue.2
, pp. 7-21
-
-
Rubtsov, N.B.1
Karamysheva, T.V.2
-
21
-
-
0029031712
-
Cytogenetic and Clinical Correlates in AML Patients with Abnormalities of Chromosome 16
-
Marlton, P., Keating, M., Kantarjian, H., et al., Cytogenetic and Clinical Correlates in AML Patients with Abnormalities of Chromosome 16, Leukemia, 1995, vol. 9, pp. 965-971.
-
(1995)
Leukemia
, vol.9
, pp. 965-971
-
-
Marlton, P.1
Keating, M.2
Kantarjian, H.3
-
22
-
-
0028999990
-
Prognostic Value of Residual Normal Metaphases in Acute Myelogenous Leukemia Patients Presenting with Abnormal Karyotype
-
Ghaddar, H.M., Pierce, S., Reed, P., and Estey, E.H., Prognostic Value of Residual Normal Metaphases in Acute Myelogenous Leukemia Patients Presenting with Abnormal Karyotype, Leukemia, 1995, vol. 9, pp. 779-782.
-
(1995)
Leukemia
, vol.9
, pp. 779-782
-
-
Ghaddar, H.M.1
Pierce, S.2
Reed, P.3
Estey, E.H.4
-
23
-
-
0024501380
-
Prognostic Impact of Cytogenetic Abnormalities in Patients with de Novo Acute Nonlymphocytic Leukemia
-
Schiffer, C.A., Lee, E.J., Tomiyasu, T., et al., Prognostic Impact of Cytogenetic Abnormalities in Patients with De Novo Acute Nonlymphocytic Leukemia, Blood, 1989, vol. 73, pp. 263-270.
-
(1989)
Blood
, vol.73
, pp. 263-270
-
-
Schiffer, C.A.1
Lee, E.J.2
Tomiyasu, T.3
-
24
-
-
0021911361
-
A Unique Pattern of Central Nervous System Relapse in Acute Myelomonocytic Leukemia Associated with Inv(16)(p13q22)
-
Holmes, R., Keating, M.J., Cork, A., et al., A Unique Pattern of Central Nervous System Relapse in Acute Myelomonocytic Leukemia Associated with Inv(16)(p13q22), Blood, 1985, vol. 65, pp. 1071-1075.
-
(1985)
Blood
, vol.65
, pp. 1071-1075
-
-
Holmes, R.1
Keating, M.J.2
Cork, A.3
-
25
-
-
0029808261
-
Improved Detection of Chromosome 16 Rearrangements in Acute Myeloid Leukemias Using 16p and 16q Specific Microdissection DNA Libraries
-
Chudoba, I., Rubtsov, N., Senger, G., et al., Improved Detection of Chromosome 16 Rearrangements in Acute Myeloid Leukemias Using 16p and 16q Specific Microdissection DNA Libraries, Oncol. Rep., 1996, no. 3, pp. 829-832.
-
(1996)
Oncol. Rep.
, Issue.3
, pp. 829-832
-
-
Chudoba, I.1
Rubtsov, N.2
Senger, G.3
-
26
-
-
0028843747
-
Complete and Precise Characterization of Marker Chro-mosomes by Amplification of Microdissection in Prenatal Diagnosis
-
Mueller-Navia, J., Nebel, A., and Schleiermacher, E., Complete and Precise Characterization of Marker Chro-mosomes by Amplification of Microdissection in Prenatal Diagnosis, Hum. Genet., 1995, vol. 96, pp. 661-667.
-
(1995)
Hum. Genet.
, vol.96
, pp. 661-667
-
-
Mueller-Navia, J.1
Nebel, A.2
Schleiermacher, E.3
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