"Cytogenetic Analysis" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Examination of CHROMOSOMES to diagnose, classify, screen for, or manage genetic diseases and abnormalities. Following preparation of the sample, KARYOTYPING is performed and/or the specific chromosomes are analyzed.
| Descriptor ID |
D020732
|
| MeSH Number(s) |
E01.370.225.500.385 E05.200.500.385 E05.242.385 E05.393.285
|
| Concept/Terms |
Cytogenetic Analysis- Cytogenetic Analysis
- Analyses, Cytogenetic
- Analysis, Cytogenetic
- Cytogenetic Analyses
- Molecular Cytogenetic Techniques
- Cytogenetic Technique, Molecular
- Cytogenetic Techniques, Molecular
- Molecular Cytogenetic Technique
- Technique, Molecular Cytogenetic
- Techniques, Molecular Cytogenetic
- Molecular Cytogenetic Technics
- Cytogenetic Technic, Molecular
- Cytogenetic Technics, Molecular
- Molecular Cytogenetic Technic
- Technic, Molecular Cytogenetic
- Technics, Molecular Cytogenetic
- Cytogenetic Technics
- Cytogenetic Technic
- Technic, Cytogenetic
- Technics, Cytogenetic
- Cytogenetic Techniques
- Cytogenetic Technique
- Technique, Cytogenetic
- Techniques, Cytogenetic
|
Below are MeSH descriptors whose meaning is more general than "Cytogenetic Analysis".
Below are MeSH descriptors whose meaning is more specific than "Cytogenetic Analysis".
This graph shows the total number of publications written about "Cytogenetic Analysis" by people in this website by year, and whether "Cytogenetic Analysis" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2002 | 0 | 2 | 2 |
| 2003 | 0 | 1 | 1 |
| 2004 | 0 | 1 | 1 |
| 2005 | 0 | 2 | 2 |
| 2009 | 1 | 0 | 1 |
| 2014 | 0 | 2 | 2 |
| 2017 | 0 | 1 | 1 |
| 2018 | 0 | 1 | 1 |
| 2019 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Cytogenetic Analysis" by people in Profiles.
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Distinct pathways associated with chromosomal aberration frequency in a cohort exposed to genotoxic compounds compared to general population. Mutagenesis. 2019 12 19; 34(4):323-330.
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Genetic variation associated with chromosomal aberration frequency: A genome-wide association study. Environ Mol Mutagen. 2019 01; 60(1):17-28.
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Smoldering Development of Acute Megakaryoblastic Leukemia with Clonal Evolution in an Infant without Down Syndrome. Klin Padiatr. 2017 11; 229(6):352-354.
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Mutations in CKAP2L, the human homolog of the mouse Radmis gene, cause Filippi syndrome. Am J Hum Genet. 2014 Nov 06; 95(5):622-32.
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[Alopecia and hypotrichosis in childhood: clinical features and diagnosis]. Hautarzt. 2014 Jun; 65(6):520-6.
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A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients. Eur J Hum Genet. 2009 Dec; 17(12):1592-9.
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Genomic affinities in Arachis section Arachis (Fabaceae): molecular and cytogenetic evidence. Theor Appl Genet. 2005 Nov; 111(7):1229-37.
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Gene expression in kidney cancer is associated with cytogenetic abnormalities, metastasis formation, and patient survival. Clin Cancer Res. 2005 Jan 15; 11(2 Pt 1):646-55.
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Circulating tumor cells in patients with breast cancer dormancy. Clin Cancer Res. 2004 Dec 15; 10(24):8152-62.
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Distal monosomy 18p/distal trisomy 20p--a recognizable facial phenotype? Am J Med Genet A. 2003 Jul 30; 120A(3):429-33.
MeSH information
