Chromosomes, Human, Pair 18
"Chromosomes, Human, Pair 18" 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 E CHROMOSOMES of the human chromosome classification.
| Descriptor ID |
D002887
|
| MeSH Number(s) |
A11.284.187.520.300.415.430 G05.360.162.520.300.415.430
|
| Concept/Terms |
|
Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, Pair 18".
- 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, 16-18 [A11.284.187.520.300.415]
- Chromosomes, Human, Pair 18 [A11.284.187.520.300.415.430]
- 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, 16-18 [G05.360.162.520.300.415]
- Chromosomes, Human, Pair 18 [G05.360.162.520.300.415.430]
Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, Pair 18".
This graph shows the total number of publications written about "Chromosomes, Human, Pair 18" by people in this website by year, and whether "Chromosomes, Human, Pair 18" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 1996 | 1 | 0 | 1 |
| 2002 | 2 | 0 | 2 |
| 2003 | 0 | 1 | 1 |
| 2005 | 2 | 0 | 2 |
| 2007 | 1 | 0 | 1 |
| 2009 | 1 | 1 | 2 |
| 2012 | 0 | 1 | 1 |
| 2016 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosomes, Human, Pair 18" by people in Profiles.
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Trisomy 18: A survey of opinions, attitudes, and practices of neonatologists. Am J Med Genet A. 2016 10; 170(10):2638-43.
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Patient choice and clinical outcomes following positive noninvasive prenatal screening for aneuploidy with cell-free DNA (cfDNA). Prenat Diagn. 2016 May; 36(5):456-62.
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Trisomy 18: A single-center evaluation of management trends and experience with aggressive obstetric or neonatal intervention. Am J Med Genet A. 2016 Apr; 170A(4):838-46.
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Array-comparative genomic hybridization reveals loss of SOCS6 is associated with poor prognosis in primary lung squamous cell carcinoma. PLoS One. 2012; 7(2):e30398.
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Narrowing critical regions and determining penetrance for selected 18q- phenotypes. Am J Med Genet A. 2009 Jul; 149A(7):1421-30.
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Linkage analysis of albuminuria. J Am Soc Nephrol. 2009 Jul; 20(7):1597-606.
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Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1. Am J Hum Genet. 2007 Jul; 81(1):180-8.
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Growth hormone benefits children with 18q deletions. Am J Med Genet A. 2005 Aug 15; 137(1):9-15.
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The spectrum of thyroid abnormalities in individuals with 18q deletions. J Clin Endocrinol Metab. 2005 Apr; 90(4):2259-63.
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Double trisomy. Am J Med Genet A. 2004 Jan 01; 124A(1):96-8.