"Twins, Monozygotic" 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.
Two off-spring from the same PREGNANCY. They are from a single fertilized OVUM that split into two EMBRYOS. Such twins are usually genetically identical and of the same sex.
Descriptor ID |
D014430
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MeSH Number(s) |
M01.438.873.940
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Concept/Terms |
Twins, Monozygotic- Twins, Monozygotic
- Monozygotic Twin
- Monozygotic Twins
- Twin, Monozygotic
- Twins, Identical
- Identical Twin
- Identical Twins
- Twin, Identical
|
Below are MeSH descriptors whose meaning is more general than "Twins, Monozygotic".
Below are MeSH descriptors whose meaning is more specific than "Twins, Monozygotic".
This graph shows the total number of publications written about "Twins, Monozygotic" by people in this website by year, and whether "Twins, Monozygotic" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1995 | 0 | 1 | 1 |
2006 | 1 | 1 | 2 |
2010 | 1 | 0 | 1 |
2011 | 1 | 1 | 2 |
2015 | 1 | 0 | 1 |
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Below are the most recent publications written about "Twins, Monozygotic" by people in Profiles.
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Rapid-Onset Obesity with Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD): exome sequencing of trios, monozygotic twins and tumours. Orphanet J Rare Dis. 2015 Aug 25; 10:103.
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Advancing paternal age and simplex autism. Autism. 2012 Jul; 16(4):367-80.
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Monozygotic twins discordant for ROHHAD phenotype. Pediatrics. 2011 Sep; 128(3):e711-5.
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Failure to confirm CNVs as of aetiological significance in twin pairs discordant for schizophrenia. Twin Res Hum Genet. 2010 Oct; 13(5):455-60.
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Chiari in the family: inheritance of the Chiari I malformation. Pediatr Neurol. 2006 Jun; 34(6):481-5.
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Premature monozygotic twins with bilateral choanal atresia: a case report. Laryngoscope. 2006 Jan; 116(1):149-50.
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The childhood growth of twin children. Acta Genet Med Gemellol (Roma). 1995; 44(3-4):169-78.