"Abnormal Karyotype" 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 variation from the normal set of chromosomes characteristic of a species.
| Descriptor ID |
D059786
|
| MeSH Number(s) |
C23.550.210.024 G05.360.162.679.500 G05.365.590.175.024
|
| Concept/Terms |
Abnormal Karyotype- Abnormal Karyotype
- Abnormal Karyotypes
- Karyotypes, Abnormal
- Karyotype, Abnormal
|
Below are MeSH descriptors whose meaning is more general than "Abnormal Karyotype".
Below are MeSH descriptors whose meaning is more specific than "Abnormal Karyotype".
This graph shows the total number of publications written about "Abnormal Karyotype" by people in this website by year, and whether "Abnormal Karyotype" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2012 | 0 | 2 | 2 |
| 2018 | 1 | 0 | 1 |
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Below are the most recent publications written about "Abnormal Karyotype" by people in Profiles.
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Genetic abnormalities seen on CVS in early pregnancy failure. J Matern Fetal Neonatal Med. 2020 Jul; 33(13):2142-2147.
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Progress in acute myeloid leukemia. Clin Lymphoma Myeloma Leuk. 2015 Mar; 15(3):139-51.
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Complex or monosomal karyotype and not blast percentage is associated with poor survival in acute myeloid leukemia and myelodysplastic syndrome patients with inv(3)(q21q26.2)/t(3;3)(q21;q26.2): a Bone Marrow Pathology Group study. Haematologica. 2014 May; 99(5):821-9.
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Monoclonality and cytogenetic abnormalities in hyaline vascular Castleman disease. Mod Pathol. 2014 Jun; 27(6):823-31.
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B acute lymphoblastic leukemia with t(14;19)(q32;p13.1) involving IGH/EPOR: a clinically aggressive subset of disease. Mod Pathol. 2014 Mar; 27(3):382-9.
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Systemic mastocytosis with associated clonal hematological non-mast cell lineage disease: clinical significance and comparison of chomosomal abnormalities in SM and AHNMD components. Am J Hematol. 2013 Mar; 88(3):219-24.
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Molecular characterization of de novo Philadelphia chromosome-positive acute myeloid leukemia. Leuk Lymphoma. 2013 Jan; 54(1):138-44.
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Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature. Prenat Diagn. 2012 Apr; 32(4):351-61.
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Ewing sarcoma with 7;22 translocation: three new cases and clinicopathological characterization. Fetal Pediatr Pathol. 2012 Dec; 31(6):341-8.