-
1
-
-
0028956847
-
Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ hybridization
-
ABUELO D., Mark H. F. L. and Bier L. 1995. Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ hybridization. Clin. Pediatrics 34 223-6.
-
(1995)
Clin. Pediatrics
, vol.34
, pp. 223-226
-
-
Abuelo, D.1
Mark, H.F.L.2
Bier, L.3
-
2
-
-
0029937912
-
Fluorescent in situ hybridization assessment of chromosome copy number in breast cancer
-
AFIFY A., Bland K. I. and Mark H. F .L. 1996. Fluorescent in situ hybridization assessment of chromosome copy number in breast cancer. Breast Cancer Res.Treatment 38 201-8.
-
(1996)
Breast Cancer Res.Treatment
, vol.38
, pp. 201-208
-
-
Afify, A.1
Bland, K.I.2
Mark, H.F.L.3
-
3
-
-
0020571801
-
Cytological types of mitoses and chromosome abnormalities in acute leukemia
-
BERGER R., Bernheim A., Daniel M-T., Valensi F. and Flandrin G. 1983. Cytological types of mitoses and chromosome abnormalities in acute leukemia. Leuk. Res. 7 221-36.
-
(1983)
Leuk. Res.
, vol.7
, pp. 221-236
-
-
Berger, R.1
Bernheim, A.2
Daniel, M.-T.3
Valensi, F.4
Flandrin, G.5
-
4
-
-
0027764525
-
Establishment of biologically heterogeneous cell lines from primary cervical tumors of different histological grade
-
BRAUN L., Mikimo R., Mark H. F. L. and Lauchlan S. 1993. Establishment of biologically heterogeneous cell lines from primary cervical tumors of different histological grade. Am. J. Path. 143 832-44.
-
(1993)
Am. J. Path.
, vol.143
, pp. 832-844
-
-
Braun, L.1
Mikimo, R.2
Mark, H.F.L.3
Lauchlan, S.4
-
5
-
-
0027447828
-
Trisomy 8 as a recurrent clonal abnormality in breast cancer
-
BULLERDIEK J., Leuschner E., Taquia E., Bonk U. and Bartnitzke S. 1993. Trisomy 8 as a recurrent clonal abnormality in breast cancer. Cancer Genet. Cytogenet. 65 64-7.
-
(1993)
Cancer Genet. Cytogenet.
, vol.65
, pp. 64-67
-
-
Bullerdiek, J.1
Leuschner, E.2
Taquia, E.3
Bonk, U.4
Bartnitzke, S.5
-
7
-
-
0026322890
-
Trisomy 8 as the only chromosome change in an epithelioid smooth muscle tumor
-
DAL CIN P., deWever I., Aerts R., Van Damme B. and Van Den Berghe H. 1991. Trisomy 8 as the only chromosome change in an epithelioid smooth muscle tumor. Gene Chrom. Cancer 3 235-7.
-
(1991)
Gene Chrom. Cancer
, vol.3
, pp. 235-237
-
-
Dal Cin, P.1
DeWever, I.2
Aerts, R.3
Van Damme, B.4
Van Den Berghe, H.5
-
8
-
-
0028922626
-
Chromosome aberrations in desmoid tumors. Trisomy 8 may be a predictor of recurrence
-
FLETCHER J. A., Naeem R., Xiao S. and Corson J. 1995. Chromosome aberrations in desmoid tumors. Trisomy 8 may be a predictor of recurrence. Cancer Genet. Cytogenet. 79 139-43.
-
(1995)
Cancer Genet. Cytogenet.
, vol.79
, pp. 139-143
-
-
Fletcher, J.A.1
Naeem, R.2
Xiao, S.3
Corson, J.4
-
9
-
-
0027972451
-
Functional characteristics of in vivo induced neutrophils after differentiation therapy of acute promyelocytic leukemia with all-trans-retinoic acid
-
GLASSER L., Fiederlein R. L., Shamdas G. J. and Brothman, A. R. 1994. Functional characteristics of in vivo induced neutrophils after differentiation therapy of acute promyelocytic leukemia with all-trans-retinoic acid. Cancer 73 1206-12.
-
(1994)
Cancer
, vol.73
, pp. 1206-1212
-
-
Glasser, L.1
Fiederlein, R.L.2
Shamdas, G.J.3
Brothman, A.R.4
-
10
-
-
0027957296
-
Acute promelocytic leukaemia: From genetics to treatment.
-
Review
-
GRIGNANI F., Fagioli M., Akalay M., Longo L., Pandolfi P. P., Donti E., Biondi A., Coco F. L., Grignani F. and Pelicci P. 1994. Acute promelocytic leukaemia: from genetics to treatment. (Review). Blood 83 10-25.
-
(1994)
Blood
, vol.83
, pp. 10-25
-
-
Grignani, F.1
Fagioli, M.2
Akalay, M.3
Longo, L.4
Pandolfi, P.P.5
Donti, E.6
Biondi, A.7
Coco, F.L.8
Grignani, F.9
Pelicci, P.10
-
11
-
-
0013471218
-
Genetic heterogeneity of acute myeloid leukemia (AML) with FAB-AML M3 morphology
-
abstract
-
HEAD D. R., Behm F., Raimondi S., Carroll A., Slovak M., Magenis E., Willman C., Licht J., Scott A., Gresik M. V., Downing J., Butler D. and Motroni T. 1995. Genetic heterogeneity of acute myeloid leukemia (AML) with FAB-AML M3 morphology. Lab. Invest. 72 112A (abstract).
-
(1995)
Lab. Invest.
, vol.72
-
-
Head, D.R.1
Behm, F.2
Raimondi, S.3
Carroll, A.4
Slovak, M.5
Magenis, E.6
Willman, C.7
Licht, J.8
Scott, A.9
Gresik, M.V.10
Downing, J.11
Butler, D.12
Motroni, T.13
-
13
-
-
84891583465
-
-
Second editn. Wiley-Liss, New York
-
HEIM S. and Mitelman F. 1995. Cancer Cytogenetics. pp 96-100. Second editn. Wiley-Liss, New York.
-
(1995)
Cancer Cytogenetics
, pp. 96-100
-
-
Heim, S.1
Mitelman, F.2
-
14
-
-
0025107845
-
Leiomyosarcoma in a patient with trisomy 8 mosaicism
-
LESSICK M., Israel J., Szego J., Szego K. and Wong P. 1990. Leiomyosarcoma in a patient with trisomy 8 mosaicism. J. Med. Genet. 27 643-4.
-
(1990)
J. Med. Genet.
, vol.27
, pp. 643-644
-
-
Lessick, M.1
Israel, J.2
Szego, J.3
Szego, K.4
Wong, P.5
-
15
-
-
0024695758
-
Non-random numerical chromosome aberrations (+8, +11, +17, +20) in infantile fibrosarcoma
-
MANDAHL N., Heim S., Rydholm A. and Mitelman F. 1989. Non-random numerical chromosome aberrations (+8, +11, +17, +20) in infantile fibrosarcoma. Cancer Genet. Cytogenet. 40 137-8.
-
(1989)
Cancer Genet. Cytogenet.
, vol.40
, pp. 137-138
-
-
Mandahl, N.1
Heim, S.2
Rydholm, A.3
Mitelman, F.4
-
17
-
-
0028803893
-
Localization of the gene encoding the secretin receptor on human chromosome 2q by fluorescent in situ hybridization and chromosome morphometry
-
MARK H. F. L. and Chow B. 1995. Localization of the gene encoding the secretin receptor on human chromosome 2q by fluorescent in situ hybridization and chromosome morphometry. Genomics 29 817-8.
-
(1995)
Genomics
, vol.29
, pp. 817-818
-
-
Mark, H.F.L.1
Chow, B.2
-
18
-
-
0029078935
-
Fluorescent in situ hybridization (FISH) assessment of chromosome copy number in gestational trophoblastic disease
-
MARK H. F. L., Grollino M. G., Sulaiman R. A. and Lathrop J. C. 1995a. Fluorescent in situ hybridization (FISH) assessment of chromosome copy number in gestational trophoblastic disease. Ann. Clin. Lab. Sci. 25 291-6.
-
(1995)
Ann. Clin. Lab. Sci.
, vol.25
, pp. 291-296
-
-
Mark, H.F.L.1
Grollino, M.G.2
Sulaiman, R.A.3
Lathrop, J.C.4
-
19
-
-
0028922877
-
Cytogenetic characterization of three cell lines derived from primary cervical tumors
-
MARK H. F. L., Hann E., Mikumo R., Lauchlan S., Beauregard L. and Braun L. 1995b. Cytogenetic characterization of three cell lines derived from primary cervical tumors. Ann. Clin. Lab. Sci. 25 193-207.
-
(1995)
Ann. Clin. Lab. Sci.
, vol.25
, pp. 193-207
-
-
Mark, H.F.L.1
Hann, E.2
Mikumo, R.3
Lauchlan, S.4
Beauregard, L.5
Braun, L.6
-
20
-
-
0029012822
-
Fluorescent in situ hybridization for assessing the proportion of cells with trisomy 4 in a patient with acute non-lymphoblastic leukemia
-
MARK H. F. L., Sikov W., Safran H., King T. C. and Griffith R. C. 1995c. Fluorescent in situ hybridization for assessing the proportion of cells with trisomy 4 in a patient with acute non-lymphoblastic leukemia. Ann. Clin. Lab. Sci. 25 330-5.
-
(1995)
Ann. Clin. Lab. Sci.
, vol.25
, pp. 330-335
-
-
Mark, H.F.L.1
Sikov, W.2
Safran, H.3
King, T.C.4
Griffith, R.C.5
-
21
-
-
0029435942
-
Towards the development of a fluorescent in situ hybridization based genotoxicologic assay for aneuploidy detection in sperm
-
MARK H. F. L., Sheu M., Lopes L., Mulholland J., Takezawa K. and Sigman M. 1995d. Towards the development of a fluorescent in situ hybridization based genotoxicologic assay for aneuploidy detection in sperm. Cytobios 82 171-80.
-
(1995)
Cytobios
, vol.82
, pp. 171-180
-
-
Mark, H.F.L.1
Sheu, M.2
Lopes, L.3
Mulholland, J.4
Takezawa, K.5
Sigman, M.6
-
22
-
-
0029128053
-
Assessment of sex chromosome composition using FISH as an adjunct to GTG-banding
-
MARK H. F. L., Meyers-Seifer C., Seifer D., DeMoranville B. and Jackson I. M. 1995e. Assessment of sex chromosome composition using FISH as an adjunct to GTG-banding. Ann. Clin. Lab. Sci. 25 402-8.
-
(1995)
Ann. Clin. Lab. Sci.
, vol.25
, pp. 402-408
-
-
Mark, H.F.L.1
Meyers-Seifer, C.2
Seifer, D.3
DeMoranville, B.4
Jackson, I.M.5
-
23
-
-
0029063603
-
Constitutional trisomy 8 mosaicism and gestational trophoblastic disease
-
MARK H. F. L., Ahearn I. and Lathrop J. C. 1995f. Constitutional trisomy 8 mosaicism and gestational trophoblastic disease. Cancer Genet. Cytogenet. 80 150-4.
-
(1995)
Cancer Genet. Cytogenet.
, vol.80
, pp. 150-154
-
-
Mark, H.F.L.1
Ahearn, I.2
Lathrop, J.C.3
-
24
-
-
0029084670
-
Laboratory Practices: Impact of regulations on genetic testing
-
MARK H. F. L., Kelly T., Watson M. S., Hoeltge J., Miller W. A. and Beauregard L. 1995g. Laboratory Practices: impact of regulations on genetic testing. J. med. Gen. 32 780-6.
-
(1995)
J. Med. Gen.
, vol.32
, pp. 780-786
-
-
Mark, H.F.L.1
Kelly, T.2
Watson, M.S.3
Hoeltge, J.4
Miller, W.A.5
Beauregard, L.6
-
25
-
-
0011899766
-
Characterization of chromosome 9 and 19 somatic cell and radiation hybrids: A comparison of approaches
-
MARK H. F. L., Santoro K. and Jackson C. 1992. Characterization of chromosome 9 and 19 somatic cell and radiation hybrids: a comparison of approaches. Appl. Cytogenet. 18 149-56.
-
(1992)
Appl. Cytogenet.
, vol.18
, pp. 149-156
-
-
Mark, H.F.L.1
Santoro, K.2
Jackson, C.3
-
26
-
-
0028345430
-
Fluorescent in situ hybridization as an adjunct to conventional cytogenetics
-
MARK H. F. L. 1994a Fluorescent in situ hybridization as an adjunct to conventional cytogenetics. Ann. Clin. Lab. Sci. 24 153-63.
-
(1994)
Ann. Clin. Lab. Sci.
, vol.24
, pp. 153-163
-
-
Mark, H.F.L.1
-
27
-
-
0002833043
-
Bone marrow cytogenetics and hematologic malignancies
-
The Association of Cytogenetic Technologists
-
MARK H. F. L. 1994b Bone marrow cytogenetics and hematologic malignancies. In The Cytogenetic Symposia, Burbank, California, pp 8-1 to 8-7. The Association of Cytogenetic Technologists.
-
(1994)
The Cytogenetic Symposia, Burbank, California
, pp. 8-11
-
-
Mark, H.F.L.1
-
28
-
-
0028541554
-
Evolving standards of practice for clinical cytogenetics
-
MARK H. F. L. and Watson M. 1994. Evolving standards of practice for clinical cytogenetics. Rhode Island Med. 77 373-4.
-
(1994)
Rhode Island Med.
, vol.77
, pp. 373-374
-
-
Mark, H.F.L.1
Watson, M.2
-
29
-
-
0028099486
-
Fluorescent in situ hybridization in routinely processed bone marrow aspirate clot and core biopsy section
-
MIRANDA R. N., Mark H. F. L. and Medeiros U. 1994. Fluorescent in situ hybridization in routinely processed bone marrow aspirate clot and core biopsy section. Am. J. Path. 145 1-6.
-
(1994)
Am. J. Path.
, vol.145
, pp. 1-6
-
-
Miranda, R.N.1
Mark, H.F.L.2
Medeiros, U.3
-
30
-
-
0025923601
-
Leiomyosarcoma in a patient with trisomy 8 mosaicism. Letters, comments
-
MOLENAAR W., DeJong B. and Van den Berg E. 1991. Leiomyosarcoma in a patient with trisomy 8 mosaicism. (Letters, comments). J. med. Genet. 28 724-5.
-
(1991)
J. Med. Genet.
, vol.28
, pp. 724-725
-
-
Molenaar, W.1
DeJong, B.2
Van Den Berg, E.3
-
31
-
-
0013663724
-
Chromosome preparation of leukocytes cultured from human peripheral blood
-
MOORHEAD P., Nowell P. and Mellman W. 1960. Chromosome preparation of leukocytes cultured from human peripheral blood. Expl Cell Res. 20 613-6.
-
(1960)
Expl Cell Res.
, vol.20
, pp. 613-616
-
-
Moorhead, P.1
Nowell, P.2
Mellman, W.3
-
32
-
-
0022446922
-
Cytogenetic analysis using quantitative high-sensitivity, fluorescence hybridization
-
PINKEL D., Strawne R. and Gray J. W. 1986. Cytogenetic analysis using quantitative high-sensitivity, fluorescence hybridization. Proc. natn. Acad. Sci. U.S.A. 83 2934-8.
-
(1986)
Proc. Natn. Acad. Sci. U.S.A.
, vol.83
, pp. 2934-2938
-
-
Pinkel, D.1
Strawne, R.2
Gray, J.W.3
-
33
-
-
0001805746
-
Malignant and acquired abnormalities
-
Edited by D. E. Rooney and B. H. Czepulkowski. IRL Press, Oxford
-
POTTER A. M. and Watmore A. 1992. Malignant and acquired abnormalities. In Human Cytogenetics. Vol II, pp 27-66. Edited by D. E. Rooney and B. H. Czepulkowski. IRL Press, Oxford.
-
(1992)
Human Cytogenetics
, vol.2
, pp. 27-66
-
-
Potter, A.M.1
Watmore, A.2
-
34
-
-
0028961075
-
Trisomy 8 and 18 as frequent clonal and single-cell aberrations in 185 primary breast carcinomas
-
ROHEN C., Meyer-Bolte K., Bonk U., Ebel T., Staats B., Leuschmer E., Gohla G., Caselitz J., Bartnitzke S. and Bullerdiek J. 1995. Trisomy 8 and 18 as frequent clonal and single-cell aberrations in 185 primary breast carcinomas. Cancer Genet. Cytogenet 80 33-9.
-
(1995)
Cancer Genet. Cytogenet
, vol.80
, pp. 33-39
-
-
Rohen, C.1
Meyer-Bolte, K.2
Bonk, U.3
Ebel, T.4
Staats, B.5
Leuschmer, E.6
Gohla, G.7
Caselitz, J.8
Bartnitzke, S.9
Bullerdiek, J.10
-
35
-
-
0017362792
-
15/17 translocation, a consistent chromosomal change in acute promyelocytic leukaemia
-
ROWLEY J. D., Golomb H. M. and Dougherty C. 1977. 15/17 translocation, a consistent chromosomal change in acute promyelocytic leukaemia. Lancet 1 549-50.
-
(1977)
Lancet
, vol.1
, pp. 549-550
-
-
Rowley, J.D.1
Golomb, H.M.2
Dougherty, C.3
-
36
-
-
0028053585
-
Efficacy of fluorescence in situ hybridization for detecting PML/RARA gene fusion in treated and untreated acute promyelocytic leukemia
-
SCHAD C. R., Hanson C. A., Paietta E., Casper J., Jalal S. M. and Dewald G. W. 1994. Efficacy of fluorescence in situ hybridization for detecting PML/RARA gene fusion in treated and untreated acute promyelocytic leukemia. Mayo Clin. Proc. 69 1047-53.
-
(1994)
Mayo Clin. Proc.
, vol.69
, pp. 1047-1053
-
-
Schad, C.R.1
Hanson, C.A.2
Paietta, E.3
Casper, J.4
Jalal, S.M.5
Dewald, G.W.6
-
37
-
-
0028179858
-
HLA-DR-, CD33+, CD56+, CD16- myeloid/natural killer cell acute leukemia: A previously unrecognized form of acute leukemia potentially misdiagnosed as French-American-British acute myeloid leukemia-M3
-
SCOTT A. A., Head D. R., Kopecky K. J., Appelbaum F. R., Theil K. S., Grever M. R., Chen I. M., Whittaker M. H., Griffith B. B. and Licht J. D. 1994. HLA-DR-, CD33+, CD56+, CD16- myeloid/natural killer cell acute leukemia: a previously unrecognized form of acute leukemia potentially misdiagnosed as French-American-British acute myeloid leukemia-M3. Blood 84 244-55.
-
(1994)
Blood
, vol.84
, pp. 244-255
-
-
Scott, A.A.1
Head, D.R.2
Kopecky, K.J.3
Appelbaum, F.R.4
Theil, K.S.5
Grever, M.R.6
Chen, I.M.7
Whittaker, M.H.8
Griffith, B.B.9
Licht, J.D.10
-
38
-
-
0015246254
-
A rapid banding technique for human chromosomes
-
SEABRIGHT M. A. 1971. A rapid banding technique for human chromosomes. Lancet 2 971-2.
-
(1971)
Lancet
, vol.2
, pp. 971-972
-
-
Seabright, M.A.1
-
39
-
-
0015213950
-
New technique for distinguishing between human chromosomes
-
SUMNER A. T., Evan H. J. and Buckland R. A. 1971. New technique for distinguishing between human chromosomes. Nature 232 31-2.
-
(1971)
Nature
, vol.232
, pp. 31-32
-
-
Sumner, A.T.1
Evan, H.J.2
Buckland, R.A.3
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