"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
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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 |
---|
2004 | 0 | 1 | 1 |
2008 | 0 | 1 | 1 |
2010 | 0 | 1 | 1 |
2012 | 1 | 1 | 2 |
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click here.
Below are the most recent publications written about "Cytogenetic Analysis" by people in Profiles.
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Acute Myeloid Leukemia, Version 3.2019, NCCN Clinical Practice Guidelines in Oncology. J Natl Compr Canc Netw. 2019 06 01; 17(6):721-749.
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Impact of the optical depth of field on cytogenetic image quality. J Biomed Opt. 2012 Sep; 17(9):96017-1.
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Low-grade sinonasal sarcoma with neural and myogenic features: a clinicopathologic analysis of 28 cases. Am J Surg Pathol. 2012 Apr; 36(4):517-25.
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De novo generation of white adipocytes from the myeloid lineage via mesenchymal intermediates is age, adipose depot, and gender specific. Proc Natl Acad Sci U S A. 2010 Aug 17; 107(33):14781-6.
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Sporadic hybrid oncocytic/chromophobe tumor of the kidney: a clinicopathologic, histomorphologic, immunohistochemical, ultrastructural, and molecular cytogenetic study of 14 cases. Virchows Arch. 2010 Apr; 456(4):355-65.
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Detection of chromosomal aberrations in renal tumors: a comparative study of conventional cytogenetics and virtual karyotyping with single-nucleotide polymorphism microarrays. Arch Pathol Lab Med. 2009 Dec; 133(12):1917-22.
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Deletion of 14q24.1 approximately q24.3 in a patient with acute lymphoblastic leukemia: a hidden chromosomal anomaly detected by array-based comparative genomic hybridization. Cancer Genet Cytogenet. 2008 Aug; 185(1):43-6.
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De novo three-way chromosome translocation 46,XY,t(4;6;21)(p16;p21.1;q21) in a male with cleidocranial dysplasia. Am J Med Genet A. 2008 Feb 15; 146A(4):453-8.
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A variant t(8;10;21) in a patient with pathological features mimicking atypical chronic myeloid leukemia. Cancer Genet Cytogenet. 2005 May; 159(1):79-83.
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A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome. Clin Genet. 2004 May; 65(5):400-4.