"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.
To see the data from this visualization as text,
click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 1 | 0 | 1 |
| 2006 | 1 | 1 | 2 |
| 2009 | 1 | 0 | 1 |
| 2010 | 1 | 1 | 2 |
| 2016 | 1 | 0 | 1 |
| 2017 | 1 | 0 | 1 |
| 2021 | 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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Salivary and Dental Complications in Childhood Cancer Survivors Treated With Radiation Therapy to the Head and Neck: A PENTEC Comprehensive Review. Int J Radiat Oncol Biol Phys. 2024 Jun 01; 119(2):467-481.
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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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Craniofacial and Dental Defects in the Col1a1Jrt/+ Mouse Model of Osteogenesis Imperfecta. J Dent Res. 2016 07; 95(7):761-8.
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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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Functional analysis of Ectodysplasin-A mutations causing selective tooth agenesis. Eur J Hum Genet. 2010 Jan; 18(1):19-25.
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Genetics and human malformations. J Craniofac Surg. 2009 Sep; 20 Suppl 2:1652-4.
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Incontinentia pigmenti in male patients. J Am Acad Dermatol. 2006 Aug; 55(2):251-5.
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Molecular characterization of a novel PAX9 missense mutation causing posterior tooth agenesis. Eur J Hum Genet. 2006 Apr; 14(4):403-9.
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Management of eyelid anomalies associated with Blepharo-cheilo-dontic syndrome. Am J Ophthalmol. 2001 Aug; 132(2):279-80.
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The bed anomalies in anthropological illumination. Sver Tandlakarforb Tidn. 1948 May 01; 40(9):211-25.