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Chromosome Aberrations
Known as:
Abnormalities, Chromosomal
, Aberrations, Chromosomal
, Aberration, Cytogenetic
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An irregularity in the number or structure of chromosomes, usually in the form of a gain (duplication), loss (deletion), exchange (translocation), or…
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National Institutes of Health
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Related topics
Related topics
44 relations
Narrower (20)
47, XYY syndrome
Aneuploidy
Autosomal deletion syndromes
Autosome Abnormalities
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Chromosome 13q deletion syndrome
Chromosomes
Complete trisomy 18 syndrome
Congenital chromosomal disease
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Broader (5)
Congenital Disorders
Fetal Diseases
Gene Mutation
Hereditary Diseases
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Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2000
Highly Cited
2000
Inactivation of mouse Hus1 results in genomic instability and impaired responses to genotoxic stress.
Robert S. Weiss
,
Tamar Enoch
,
Philip Leder
Genes & Development
2000
Corpus ID: 38240560
The eukaryotic cell cycle is overseen by regulatory mechanisms, termed checkpoints, that respond to DNA damage, mitotic spindle…
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Highly Cited
1995
Highly Cited
1995
Cloning and characterization of murine p16INK4a and p15INK4b genes.
Dawn E. Quelle
,
R. Ashmun
,
+7 authors
M. Serrano
Oncogene
1995
Corpus ID: 21979822
Progression through the G1 phase of the cell cycle is regulated in part by the D-type cyclin-dependent kinases, cdk4 and cdk6…
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Highly Cited
1995
Highly Cited
1995
TTF, a gene encoding a novel small G protein, fuses to the lymphoma-associated LAZ3 gene by t(3;4) chromosomal translocation.
E. Dallery
,
Sylvie Galiègue-Zouitina
,
+7 authors
Christian Bastard
Oncogene
1995
Corpus ID: 39788
We have previously shown that the LAZ3/BCL6 gene encoding a potential transcription factor, is disrupted in B-diffuse large cell…
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Highly Cited
1994
Highly Cited
1994
Potential markers of prostate cancer aggressiveness detected by fluorescence in situ hybridization in needle biopsies.
Satoru Takahashi
,
J. Qian
,
+4 authors
Robert B. Jenkins
Cancer Research
1994
Corpus ID: 16789250
Fluorescence in situ hybridization (FISH) with centromere-specific probes for chromosomes 7, 8, 11, and 12 was used to evaluate…
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Highly Cited
1994
Highly Cited
1994
Aneuploidy and aneusomy of chromosome 7 detected by fluorescence in situ hybridization are markers of poor prognosis in prostate cancer.
A. Alcaraz
,
S. Takahashi
,
+5 authors
Robert B. Jenkins
Cancer Research
1994
Corpus ID: 16857944
Fluorescence in situ hybridization is a new methodology which can be used to detect cytogenetic anomalies within interphase tumor…
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Highly Cited
1987
Highly Cited
1987
Cytogenetic studies on 519 consecutive de novo acute nonlymphocytic leukemias.
R. Berger
,
G. Flandrin
,
+7 authors
F. Sigaux
Cancer Genetics and Cytogenetics
1987
Corpus ID: 3428370
Review
1986
Review
1986
Activation of cellular oncogenes in hemopoietic cells by chromosome translocation.
S. Cory
Advances in Cancer Research
1986
Corpus ID: 37946047
Highly Cited
1984
Highly Cited
1984
Recurrent chromosomal defects are found in most patients with non-Hodgkin's-lymphoma.
J. Yunis
,
M. Oken
,
A. Theologides
,
R. Howe
,
M. Kaplan
Cancer Genetics and Cytogenetics
1984
Corpus ID: 32310144
Highly Cited
1984
Highly Cited
1984
Recurrent chromosomal defects are found in most patients with acute nonlymphocytic leukemia.
J. Yunis
Cancer Genetics and Cytogenetics
1984
Corpus ID: 44912010
Highly Cited
1976
Highly Cited
1976
Clonal lines of teratocarcinoma cells in vitro: Differentiation and cytogenetic characteristics
M. McBurney
Journal of Cellular Physiology
1976
Corpus ID: 7772376
Clonal lines of embryonal carcinoma cells have been established in culture from four independently‐derived transplantable…
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