"Tooth Abnormalities" 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.
Congenital absence of or defects in structures of the teeth.
| Descriptor ID |
D014071
|
| MeSH Number(s) |
C07.650.800 C07.793.700 C16.131.850.800
|
| Concept/Terms |
Tooth Abnormalities- Tooth Abnormalities
- Abnormalities, Tooth
- Abnormality, Tooth
- Tooth Abnormality
- Teeth Abnormalities
- Abnormalities, Teeth
- Abnormality, Teeth
- Teeth Abnormality
|
Below are MeSH descriptors whose meaning is more general than "Tooth Abnormalities".
Below are MeSH descriptors whose meaning is more specific than "Tooth Abnormalities".
This graph shows the total number of publications written about "Tooth Abnormalities" by people in this website by year, and whether "Tooth Abnormalities" was a major or minor topic of these publications.
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click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2006 | 0 | 1 | 1 |
| 2009 | 0 | 1 | 1 |
| 2010 | 0 | 1 | 1 |
| 2015 | 0 | 1 | 1 |
| 2017 | 1 | 0 | 1 |
| 2022 | 1 | 0 | 1 |
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Below are the most recent publications written about "Tooth Abnormalities" by people in Profiles.
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The Seven-Step, 7-Minute Chin Augmentation. Plast Reconstr Surg. 2023 05 01; 151(5):772e-774e.
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Assessment of Temporary Crown Extensions to Correct Linguoverted Mandibular Canine Teeth in 72 Client-Owned Dogs (2012-2016). J Vet Dent. 2018 Jun; 35(2):103-113.
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Haploinsufficiency for ANKRD11-flanking genes makes the difference between KBG and 16q24.3 microdeletion syndromes: 12 new cases. Eur J Hum Genet. 2017 06; 25(6):694-701.
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Expansion of the spectrum of ITGB6-related disorders to adolescent alopecia, dentogingival abnormalities and intellectual disability. Eur J Hum Genet. 2016 08; 24(8):1223-7.
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A Geometric Classification of Jaw Deformities. J Oral Maxillofac Surg. 2015 Dec; 73(12 Suppl):S26-31.
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Signaling by FGFR2b controls the regenerative capacity of adult mouse incisors. Development. 2010 Nov; 137(22):3743-52.
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Fine-Lubinsky syndrome: managing the rare syndromic synostosis. J Plast Reconstr Aesthet Surg. 2010 Jan; 63(1):e70-2.
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Incontinentia pigmenti in male patients. J Am Acad Dermatol. 2006 Aug; 55(2):251-5.
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Molecular basis of mouse microphthalmia (mi) mutations helps explain their developmental and phenotypic consequences. Nat Genet. 1994 Nov; 8(3):256-63.
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Residual damage in mouse lungs at long intervals after cyclophosphamide treatment. Cancer Res. 1990 Apr 01; 50(7):2139-45.