"Chromosome Deletion" 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.
Actual loss of portion of a chromosome.
| Descriptor ID |
D002872
|
| MeSH Number(s) |
C23.550.210.050.500.500 G05.365.590.029.530.175 G05.365.590.175.050.500.500 G05.365.590.762.180 G05.558.800.180 G05.700.131.500.500
|
| Concept/Terms |
Partial Monosomy- Partial Monosomy
- Monosomies, Partial
- Partial Monosomies
- Monosomy, Partial
|
Below are MeSH descriptors whose meaning is more general than "Chromosome Deletion".
Below are MeSH descriptors whose meaning is more specific than "Chromosome Deletion".
This graph shows the total number of publications written about "Chromosome Deletion" by people in this website by year, and whether "Chromosome Deletion" 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 | 2 | 1 | 3 |
| 1997 | 6 | 1 | 7 |
| 1998 | 5 | 3 | 8 |
| 1999 | 2 | 2 | 4 |
| 2000 | 5 | 1 | 6 |
| 2001 | 3 | 3 | 6 |
| 2002 | 4 | 3 | 7 |
| 2003 | 6 | 5 | 11 |
| 2004 | 5 | 4 | 9 |
| 2005 | 8 | 4 | 12 |
| 2006 | 4 | 2 | 6 |
| 2007 | 11 | 4 | 15 |
| 2008 | 9 | 3 | 12 |
| 2009 | 12 | 7 | 19 |
| 2010 | 13 | 6 | 19 |
| 2011 | 6 | 8 | 14 |
| 2012 | 11 | 8 | 19 |
| 2013 | 9 | 7 | 16 |
| 2014 | 5 | 3 | 8 |
| 2015 | 6 | 5 | 11 |
| 2016 | 3 | 7 | 10 |
| 2017 | 2 | 4 | 6 |
| 2018 | 4 | 5 | 9 |
| 2019 | 3 | 6 | 9 |
| 2020 | 2 | 6 | 8 |
| 2021 | 2 | 7 | 9 |
| 2022 | 0 | 1 | 1 |
| 2023 | 0 | 4 | 4 |
| 2024 | 3 | 1 | 4 |
| 2025 | 1 | 2 | 3 |
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Below are the most recent publications written about "Chromosome Deletion" by people in Profiles.
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Whole-genome sequencing reveals individual and cohort level insights into chromosome 9p syndromes. Genome Med. 2025 Oct 24; 17(1):129.
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Development and characterization of the novel MYD88 mutated, 6q deleted BCWM.2 cell line for Waldenstr?m macroglobulinaemia. Br J Haematol. 2025 Jun; 206(6):1604-1614.
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De Novo Chromosomes 3q and 5q Chromothripsis Leads to a 5q14.3 Microdeletion Syndrome Presentation: Case Report and Review of the Literature. Am J Med Genet A. 2025 Jun; 197(6):e63975.
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An open-label study evaluating the safety and efficacy of AMO-01 for the treatment of seizures in Phelan-McDermid syndrome. HGG Adv. 2025 Apr 10; 6(2):100393.
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Comprehensive EHMT1 variants analysis broadens genotype-phenotype associations and molecular mechanisms in Kleefstra syndrome. Am J Hum Genet. 2024 Aug 08; 111(8):1605-1625.
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Expanding the phenotype of Kleefstra syndrome: speech, language and cognition in 103 individuals. J Med Genet. 2024 May 21; 61(6):578-585.
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Clinical, genetic, and cognitive correlates of seizure occurrences in Phelan-McDermid syndrome. J Neurodev Disord. 2024 May 10; 16(1):25.
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Clinical exome sequencing efficacy and phenotypic expansions involving anomalous pulmonary venous return. Eur J Hum Genet. 2023 12; 31(12):1430-1439.
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PRDM16 Deletion Is Associated With Sex-dependent Cardiomyopathy and Cardiac Mortality: A Translational, Multi-Institutional Cohort Study. Circ Genom Precis Med. 2023 08; 16(4):390-400.
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Updated consensus guidelines on the management of Phelan-McDermid syndrome. Am J Med Genet A. 2023 08; 191(8):2015-2044.