"Fetal Growth Retardation" 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.
Failure of a FETUS to attain expected GROWTH.
Descriptor ID |
D005317
|
MeSH Number(s) |
C13.703.277.370 C16.300.390 C23.550.393.450
|
Concept/Terms |
Fetal Growth Retardation- Fetal Growth Retardation
- Fetal Growth Restriction
- Intrauterine Growth Retardation
- Growth Retardation, Intrauterine
- Intrauterine Growth Restriction
|
Below are MeSH descriptors whose meaning is more general than "Fetal Growth Retardation".
Below are MeSH descriptors whose meaning is more specific than "Fetal Growth Retardation".
This graph shows the total number of publications written about "Fetal Growth Retardation" by people in this website by year, and whether "Fetal Growth Retardation" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1998 | 0 | 1 | 1 |
2006 | 0 | 1 | 1 |
2011 | 1 | 1 | 2 |
2012 | 1 | 0 | 1 |
2013 | 1 | 0 | 1 |
2014 | 1 | 1 | 2 |
2015 | 1 | 1 | 2 |
2017 | 0 | 2 | 2 |
2018 | 1 | 0 | 1 |
2021 | 0 | 1 | 1 |
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Below are the most recent publications written about "Fetal Growth Retardation" by people in Profiles.
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Mutations and variants of ONECUT1 in diabetes. Nat Med. 2021 11; 27(11):1928-1940.
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Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann-Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutations. Hum Genet. 2018 Dec; 137(11-12):921-939.
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De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction. Am J Hum Genet. 2017 Nov 02; 101(5):833-843.
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The maternal uniparental disomy of chromosome 6?(upd(6)mat) "phenotype": result of placental trisomy?6?mosaicism? Mol Genet Genomic Med. 2017 11; 5(6):668-677.
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No major contribution of IGF2 variants to the etiology of sporadic 11p15-associated imprinting disorders. Am J Med Genet A. 2016 Jan; 170A(1):283-4.
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Paternally Inherited IGF2 Mutation and Growth Restriction. N Engl J Med. 2015 Jul 23; 373(4):349-56.
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CDKN1C mutations: two sides of the same coin. Trends Mol Med. 2014 Nov; 20(11):614-22.
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Neu-Laxova syndrome is a heterogeneous metabolic disorder caused by defects in enzymes of the L-serine biosynthesis pathway. Am J Hum Genet. 2014 Sep 04; 95(3):285-93.
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Extreme growth failure is a common presentation of ligase IV deficiency. Hum Mutat. 2014 Jan; 35(1):76-85.
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Pregnancy after successful cancer treatment: what needs to be considered? Onkologie. 2012; 35(3):128-32.