"Karyotyping" 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.
Mapping of the KARYOTYPE of a cell.
| Descriptor ID |
D007621
|
| MeSH Number(s) |
E01.370.225.500.385.315 E05.200.500.385.315 E05.242.385.315 E05.393.285.475
|
| Concept/Terms |
Karyotyping- Karyotyping
- Karyotypings
- Karyotype Analysis Methods
- Analysis Method, Karyotype
- Analysis Methods, Karyotype
- Karyotype Analysis Method
- Method, Karyotype Analysis
- Methods, Karyotype Analysis
|
Below are MeSH descriptors whose meaning is more general than "Karyotyping".
Below are MeSH descriptors whose meaning is more specific than "Karyotyping".
This graph shows the total number of publications written about "Karyotyping" by people in this website by year, and whether "Karyotyping" 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 |
|---|
| 1996 | 1 | 1 | 2 |
| 1999 | 0 | 1 | 1 |
| 2002 | 0 | 1 | 1 |
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Below are the most recent publications written about "Karyotyping" by people in Profiles.
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Molecular cytogenetic characterization of human papillomavirus16-transformed foreskin keratinocyte cell line 16-MT. Cancer Genet Cytogenet. 2006 Jul 01; 168(1):36-43.
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Localization of deletion to a 300 Kb interval of chromosome 11q13 in cervical cancer. Oncogene. 2002 Aug 15; 21(36):5631-42.
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Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p. Clin Genet. 2001 Apr; 59(4):274-8.
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Candidate region for Coffin-Siris syndrome at 7q32-->34. Am J Med Genet. 2000 Jul 31; 93(3):241-3.
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A recurring pattern of chromosomal aberrations in mammary gland tumors of MMTV-cmyc transgenic mice. Genes Chromosomes Cancer. 1999 Jul; 25(3):251-60.
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Multicolour spectral karyotyping of mouse chromosomes. Nat Genet. 1996 Nov; 14(3):312-5.
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Substantial prevalence of microdeletions of the Y-chromosome in infertile men with idiopathic azoospermia and oligozoospermia detected using a sequence-tagged site-based mapping strategy. J Clin Endocrinol Metab. 1996 Apr; 81(4):1347-52.