"Cytogenetics" 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.
A subdiscipline of genetics which deals with the cytological and molecular analysis of the CHROMOSOMES, and location of the GENES on chromosomes, and the movements of chromosomes during the CELL CYCLE.
| Descriptor ID |
D003582
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| MeSH Number(s) |
H01.158.273.343.180
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Cytogenetics".
Below are MeSH descriptors whose meaning is more specific than "Cytogenetics".
This graph shows the total number of publications written about "Cytogenetics" by people in this website by year, and whether "Cytogenetics" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Cytogenetics" by people in Profiles.
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Ortiz-Ortiz KJ, Torres-Cintr?n CR, Su?rez Ramos T, Casta?eda-Avila MA, Cotto Santana LA, Tortolero-Luna G. Patterns of use of biological and genetic markers for chronic lymphocytic leukemia and acute myeloid leukemia in Puerto Rico. Cancer Med. 2023 03; 12(6):6889-6901.
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Shi M, Cipollini MJ, Crowley-Bish PA, Higgins AW, Yu H, Miron PM. Improved detection rate of cytogenetic abnormalities in chronic lymphocytic leukemia and other mature B-cell neoplasms with use of CpG-oligonucleotide DSP30 and interleukin 2 stimulation. Am J Clin Pathol. 2013 May; 139(5):662-9.
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Gupta R, Soupir CP, Johari V, Hasserjian RP. Myelodysplastic syndrome with isolated deletion of chromosome 20q: an indolent disease with minimal morphological dysplasia and frequent thrombocytopenic presentation. Br J Haematol. 2007 Oct; 139(2):265-8.
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Zilberstein M, Seibel MM. Transvaginal amniotic puncture for cytogenetic evaluation of missed abortions. Gynecol Obstet Invest. 1997; 44(4):217-20.
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Rennert OM, Frias JL, Julius RL, Lapointe D. The detection of the heterozygote and homozygote in cystic fibrosis by short term lymphocyte culture studies: a defect in RNA methylation. Clin Pediatr (Phila). 1972 Jun; 11(6):351-2.