"Fetus" 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.
The unborn young of a viviparous mammal, in the postembryonic period, after the major structures have been outlined. In humans, the unborn young from the end of the eighth week after CONCEPTION until BIRTH, as distinguished from the earlier EMBRYO, MAMMALIAN.
Descriptor ID |
D005333
|
MeSH Number(s) |
A16.378
|
Concept/Terms |
Fetal Structures- Fetal Structures
- Fetal Structure
- Structure, Fetal
- Structures, Fetal
Fetal Tissue- Fetal Tissue
- Fetal Tissues
- Tissue, Fetal
- Tissues, Fetal
|
Below are MeSH descriptors whose meaning is more general than "Fetus".
Below are MeSH descriptors whose meaning is more specific than "Fetus".
This graph shows the total number of publications written about "Fetus" by people in this website by year, and whether "Fetus" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2009 | 0 | 1 | 1 |
2010 | 0 | 1 | 1 |
2011 | 0 | 1 | 1 |
2015 | 0 | 1 | 1 |
2016 | 0 | 1 | 1 |
2017 | 1 | 0 | 1 |
2021 | 0 | 1 | 1 |
2022 | 0 | 1 | 1 |
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Below are the most recent publications written about "Fetus" by people in Profiles.
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A single center experience of prenatal parent-fetus trio exome sequencing for pregnancies with congenital anomalies. Prenat Diagn. 2022 06; 42(7):901-910.
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Bi-allelic loss-of-function variants in KIF21A cause severe fetal akinesia with arthrogryposis multiplex. J Med Genet. 2023 01; 60(1):48-56.
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Human fetal dendritic cells promote prenatal T-cell immune suppression through arginase-2. Nature. 2017 06 29; 546(7660):662-666.
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Polyhydramnios, Transient Antenatal Bartter's Syndrome, and MAGED2 Mutations. N Engl J Med. 2016 May 12; 374(19):1853-63.
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"Acquired" Dandy-Walker malformation and cerebellar hemorrhage: Usefulness of serial MRI. Eur J Paediatr Neurol. 2016 Jan; 20(1):188-91.
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CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT). Nephrol Dial Transplant. 2012 Jun; 27(6):2355-64.
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Extreme methylation values of imprinted genes in human abortions and stillbirths. Am J Pathol. 2010 Mar; 176(3):1084-90.
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Expanding CEP290 mutational spectrum in ciliopathies. Am J Med Genet A. 2009 Oct; 149A(10):2173-80.
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Reprogramming of myosin light chain 1/3 expression in muscle heterokaryons. Dev Biol. 1991 May; 145(1):28-39.