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Specific fine chromosomal defects in cancer: an overview
scientific article published on 01 June 1981
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scholarly article
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Europe PubMed Central
PubMed publication ID
6944251
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6944251%20AND%20SRC:MED&resulttype=core&format=json
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22 October 2019
title
Specific fine chromosomal defects in cancer: an overview
(English)
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stated in
Europe PubMed Central
PubMed publication ID
6944251
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6944251%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
author name string
J J Yunis
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1
1 reference
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Europe PubMed Central
PubMed publication ID
6944251
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6944251%20AND%20SRC:MED&resulttype=core&format=json
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22 October 2019
publication date
1 June 1981
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6944251
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6944251%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
published in
Human Pathology
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Europe PubMed Central
PubMed publication ID
6944251
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6944251%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
volume
12
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Europe PubMed Central
PubMed publication ID
6944251
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6944251%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
issue
6
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6944251
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6944251%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
page(s)
503-515
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6944251
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6944251%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
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A subtype of the prototypic karyotype in acute myeloid leukemia t (8; 21) (q22; q22), del 9 (q13; q23)
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Further evidence for a non-random chromosomal abnormality in acute promyelocytic leukemia
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Ph1-positive acute leukaemia and chronic granulocytic leukaemia: one or two diseases?
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Clustering of aberrations to specific chromosomes in human neoplasms. III. Incidence and geographic distribution of chromosome aberrations in 856 cases
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CHROMOSOMES, LEUKÆMIA, AND OCCUPATIONAL EXPOSURE TO LEUKÆMOGENIC AGENTS
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The ninth annual david karnofsky lecture.Treatment of acute lymphocytic leukemia
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A new chromosome anomaly in acute lymphoblastic leukemia (ALL)
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7 January 2021
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Chromosomes in acute leukemia
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Chromosomes and causation of human cancer and leukemia.XXVI. Banding studies in acute lymphoblastic leukemia (ALL)
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A new characteristic karyotypic anomaly in lymphoproliferative disorders
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The Philadelphia Chromosome (Ph1) in Adults Presenting with Acute Leukaemia: a Comparison of Ph1+ and Ph1- Patients
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t(8;14) Translocation in a Burkitt's Type of Lymphoblastic Leukaemia (L3)
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Burkitt type 14 + marker chromosome in B-cell type acute lymphocytic leukaemia
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Characteristic chromosomal abnormalities in biopsies and lymphoid-cell lines from patients with Burkitt and non-Burkitt lymphomas
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7 January 2021
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2/8 translocation in a Japanese Burkitt's lymphoma
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Crossref
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7 January 2021
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Karyotype peculiarities of malignant lymphomas
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Crossref
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7 January 2021
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Origin of the translocated segment of the 14q+ marker in non-Burkitt lymphomas
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Crossref
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7 January 2021
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CHROMOSOME DELETION IN A CASE OF RETINOBLASTOMA.
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https://api.crossref.org/works/10.1016%2FS0046-8177%2881%2980064-0
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7 January 2021
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Retinoblastoma A Model of Hereditary Fragile Chromosomal Regions
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Crossref
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7 January 2021
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Chromosomes and causation of human cancer and leukemia. XLIV. A method for chromosome analysis of solid tumors
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Crossref
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Chromosomal Constitution of Meningiomas
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Chromosomal patterns in human meningiomas
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Karyotype patterns in human meningiomas. A comparison between studies with G- and Q-banding techniques.
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Cytological and cytogenetical studies on brain tumors. 4. Identification of the missing G chromosome in human meningiomas as no. 22 by fluorescence technique.
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Distinct haematological disorder with deletion of long arm of no. 5 chromosome
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The characterization of high-resolution G-banded chromosomes of man
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G-banding patterns of high-resolution human chromosomes 6?22, X, and Y
1 reference
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7 January 2021
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Crossref
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7 January 2021
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Transposable elements and chromosomal rearrangements in cancer — a possible link
1 reference
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7 January 2021
based on heuristic
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Identifiers
DOI
10.1016/S0046-8177(81)80064-0
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6944251
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6944251%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
PubMed publication ID
6944251
1 reference
stated in
Europe PubMed Central
PubMed publication ID
6944251
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6944251%20AND%20SRC:MED&resulttype=core&format=json
retrieved
22 October 2019
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