 Chromosome Aberrations
"Chromosome Aberrations" 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.
Abnormal number or structure of chromosomes. Chromosome aberrations may result in CHROMOSOME DISORDERS.
| Descriptor ID |
D002869
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| MeSH Number(s) |
C23.550.210 G05.365.590.175
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| Concept/Terms |
Chromosome Aberrations- Chromosome Aberrations
- Aberration, Chromosome
- Aberrations, Chromosome
- Chromosome Aberration
- Abnormalities, Chromosome
- Abnormality, Chromosome
- Chromosome Abnormality
- Cytogenetic Abnormalities
- Abnormalities, Cytogenetic
- Abnormality, Cytogenetic
- Cytogenetic Abnormality
- Chromosome Abnormalities
- Cytogenetic Aberrations
- Aberration, Cytogenetic
- Aberrations, Cytogenetic
- Cytogenetic Aberration
- Abnormalities, Chromosomal
- Abnormality, Chromosomal
- Chromosomal Abnormalities
- Chromosomal Abnormality
- Chromosomal Aberrations
- Aberration, Chromosomal
- Aberrations, Chromosomal
- Chromosomal Aberration
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Below are MeSH descriptors whose meaning is more general than "Chromosome Aberrations".
Below are MeSH descriptors whose meaning is more specific than "Chromosome Aberrations".
This graph shows the total number of publications written about "Chromosome Aberrations" by people in this website by year, and whether "Chromosome Aberrations" 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 |
|---|
| 2009 | 1 | 0 | 1 | | 2013 | 1 | 0 | 1 | | 2017 | 0 | 1 | 1 | | 2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosome Aberrations" by people in Profiles.
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Shi G, Xu J, Barnes SF, Farooqi MS, Luu HS, Gotway G, Park JY. Chromosomal Microarray Reinterpretation: Applications to Pediatric Practice. J Pediatr. 2022 Apr; 243:219-223.
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Bolouri H, Farrar JE, Triche T, Ries RE, Lim EL, Alonzo TA, Ma Y, Moore R, Mungall AJ, Marra MA, Zhang J, Ma X, Liu Y, Liu Y, Auvil JMG, Davidsen TM, Gesuwan P, Hermida LC, Salhia B, Capone S, Ramsingh G, Zwaan CM, Noort S, Piccolo SR, Kolb EA, Gamis AS, Smith MA, Gerhard DS, Meshinchi S. The molecular landscape of pediatric acute myeloid leukemia reveals recurrent structural alterations and age-specific mutational interactions. Nat Med. 2018 01; 24(1):103-112.
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Nordlund J, B?cklin CL, Wahlberg P, Busche S, Berglund EC, Eloranta ML, Flaegstad T, Forestier E, Frost BM, Harila-Saari A, Heyman M, J?nsson OG, Larsson R, Palle J, R?nnblom L, Schmiegelow K, Sinnett D, S?derh?ll S, Pastinen T, Gustafsson MG, L?nnerholm G, Syv?nen AC. Genome-wide signatures of differential DNA methylation in pediatric acute lymphoblastic leukemia. Genome Biol. 2013 Sep 24; 14(9):r105.
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Butler MG, Bittel DC, Kibiryeva N, Cooley LD, Yu S. An interstitial 15q11-q14 deletion: expanded Prader-Willi syndrome phenotype. Am J Med Genet A. 2010 Feb; 152A(2):404-8.
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Yu S, Bittel DC, Kibiryeva N, Zwick DL, Cooley LD. Validation of the Agilent 244K oligonucleotide array-based comparative genomic hybridization platform for clinical cytogenetic diagnosis. Am J Clin Pathol. 2009 Sep; 132(3):349-60.
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Zyblewski SC, Hill EG, Shirali G, Atz A, Forbus G, Gonzalez J, Hlavacek A. Chromosomal anomalies influence parental treatment decisions in relation to prenatally diagnosed congenital heart disease. Pediatr Cardiol. 2009 Nov; 30(8):1105-11.
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Bittel DC, Kibiryeva N, Butler MG. Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalities. Genet Test. 2007; 11(4):467-75.
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Bittel DC, Kibiryeva N, Dasouki M, Knoll JH, Butler MG. A 9-year-old male with a duplication of chromosome 3p25.3p26.2: clinical report and gene expression analysis. Am J Med Genet A. 2006 Mar 15; 140(6):573-9.
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Ward IM, Difilippantonio S, Minn K, Mueller MD, Molina JR, Yu X, Frisk CS, Ried T, Nussenzweig A, Chen J. 53BP1 cooperates with p53 and functions as a haploinsufficient tumor suppressor in mice. Mol Cell Biol. 2005 Nov; 25(22):10079-86.
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Bittel DC, Butler MG. Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology. Expert Rev Mol Med. 2005 Jul 25; 7(14):1-20.
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