Chromosomes, Human, Pair 22
"Chromosomes, Human, Pair 22" 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 specific pair of GROUP G CHROMOSOMES of the human chromosome classification.
Descriptor ID |
D002892
|
MeSH Number(s) |
A11.284.187.520.300.505.515 G05.360.162.520.300.505.515
|
Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 22".
- Anatomy [A]
- Cells [A11]
- Cellular Structures [A11.284]
- Chromosomes [A11.284.187]
- Chromosomes, Mammalian [A11.284.187.520]
- Chromosomes, Human [A11.284.187.520.300]
- Chromosomes, Human, 21-22 and Y [A11.284.187.520.300.505]
- Chromosomes, Human, Pair 22 [A11.284.187.520.300.505.515]
- Biological Sciences [G]
- Genetic Phenomena [G05]
- Genetic Structures [G05.360]
- Chromosomes [G05.360.162]
- Chromosomes, Mammalian [G05.360.162.520]
- Chromosomes, Human [G05.360.162.520.300]
- Chromosomes, Human, 21-22 and Y [G05.360.162.520.300.505]
- Chromosomes, Human, Pair 22 [G05.360.162.520.300.505.515]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 22".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 22" by people in this website by year, and whether "Chromosomes, Human, Pair 22" 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 |
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1994 | 2 | 0 | 2 |
1995 | 2 | 2 | 4 |
1996 | 0 | 2 | 2 |
1997 | 1 | 0 | 1 |
1998 | 1 | 0 | 1 |
1999 | 2 | 2 | 4 |
2000 | 6 | 3 | 9 |
2001 | 2 | 0 | 2 |
2002 | 1 | 2 | 3 |
2003 | 1 | 3 | 4 |
2004 | 0 | 1 | 1 |
2005 | 2 | 2 | 4 |
2006 | 1 | 1 | 2 |
2007 | 2 | 1 | 3 |
2008 | 5 | 2 | 7 |
2009 | 1 | 1 | 2 |
2010 | 3 | 2 | 5 |
2011 | 0 | 5 | 5 |
2012 | 1 | 3 | 4 |
2013 | 2 | 3 | 5 |
2014 | 1 | 0 | 1 |
2015 | 0 | 4 | 4 |
2016 | 0 | 1 | 1 |
2017 | 3 | 2 | 5 |
2018 | 0 | 2 | 2 |
2020 | 0 | 2 | 2 |
2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 22" by people in Profiles.
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Translational pediatrics: clinical perspective for Phelan-McDermid syndrome and autism research. Pediatr Res. 2022 08; 92(2):373-377.
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Two Cases of Possible Familial Chronic Myeloid Leukemia in a Family with Extensive History of Cancer. Acta Haematol. 2021; 144(5):585-590.
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Chronic myeloid leukemia: 2020 update on diagnosis, therapy and monitoring. Am J Hematol. 2020 06; 95(6):691-709.
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Access to Multidisciplinary Care for Patients With 22q11.2 Deletion Syndrome: Identifying Breakdowns in the Screening Process. J Craniofac Surg. 2020 Mar/Apr; 31(2):428-431.
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Utility of copy number variants in the classification of intracranial ependymoma. Cancer Genet. 2020 01; 240:66-72.
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Heterozygous WNT1 variant causing a variable bone phenotype. Am J Med Genet A. 2018 11; 176(11):2419-2424.
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Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations. Mol Autism. 2018; 9:31.
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Chromosome 22q11 deletion in a patient with pulmonary atresia, intact ventricular septum, and confluent branch pulmonary arteries. Cardiol Young. 2018 Mar; 28(3):467-470.
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Clinical Reasoning: A common cause for Phelan-McDermid syndrome and neurofibromatosis type 2: One ring to bind them. Neurology. 2017 10 24; 89(17):e205-e209.
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Two Novel Susceptibility Loci for Prostate Cancer in Men of African Ancestry. J Natl Cancer Inst. 2017 08 01; 109(8).