"Micrognathism" 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.
Abnormally small jaw.
Descriptor ID |
D008844
|
MeSH Number(s) |
C05.500.460.457 C05.660.207.540.460.457 C07.320.440.457 C07.650.500.460.457 C16.131.621.207.540.460.457 C16.131.850.500.460.457
|
Concept/Terms |
Micrognathism- Micrognathism
- Micrognathisms
- Mandibular Micrognathism
- Mandibular Micrognathisms
- Micrognathism, Mandibular
- Micrognathisms, Mandibular
- Micrognathia
- Micrognathias
- Congenital Micrognathism
- Congenital Micrognathisms
- Micrognathism, Congenital
- Micrognathisms, Congenital
- Congenital Micrognathia
- Congenital Micrognathias
- Micrognathia, Congenital
- Micrognathias, Congenital
- Mandibular Micrognathia
- Mandibular Micrognathias
- Micrognathia, Mandibular
- Micrognathias, Mandibular
|
Below are MeSH descriptors whose meaning is more general than "Micrognathism".
Below are MeSH descriptors whose meaning is more specific than "Micrognathism".
This graph shows the total number of publications written about "Micrognathism" by people in this website by year, and whether "Micrognathism" 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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2012 | 1 | 0 | 1 |
2013 | 1 | 0 | 1 |
2014 | 1 | 0 | 1 |
2015 | 1 | 0 | 1 |
2017 | 1 | 0 | 1 |
2018 | 1 | 1 | 2 |
2019 | 2 | 0 | 2 |
2021 | 1 | 0 | 1 |
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Below are the most recent publications written about "Micrognathism" by people in Profiles.
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Maternal transmission of a mild Coffin-Siris syndrome phenotype caused by a SOX11 missense variant. Eur J Hum Genet. 2022 01; 30(1):126-132.
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Genome-Wide Analysis of the Nucleosome Landscape in Individuals with Coffin-Siris Syndrome. Cytogenet Genome Res. 2019; 159(1):1-11.
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Mutations in SMARCB1 and in other Coffin-Siris syndrome genes lead to various brain midline defects. Nat Commun. 2019 07 04; 10(1):2966.
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The ARID1B spectrum in 143 patients: from nonsyndromic intellectual disability to Coffin-Siris syndrome. Genet Med. 2019 06; 21(6):1295-1307.
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Mutations in the BAF-Complex Subunit DPF2 Are Associated with Coffin-Siris Syndrome. Am J Hum Genet. 2018 03 01; 102(3):468-479.
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Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin-Siris syndrome-like phenotype. Hum Genet. 2017 03; 136(3):297-305.
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Exome sequencing unravels unexpected differential diagnoses in individuals with the tentative diagnosis of Coffin-Siris and Nicolaides-Baraitser syndromes. Hum Genet. 2015 Jun; 134(6):553-68.
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Females with de novo aberrations in PHF6: clinical overlap of Borjeson-Forssman-Lehmann with Coffin-Siris syndrome. Am J Med Genet C Semin Med Genet. 2014 Sep; 166C(3):290-301.
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A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling. Hum Mol Genet. 2013 Dec 20; 22(25):5121-35.
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Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH. Hum Mol Genet. 2012 Sep 15; 21(18):3969-83.