 Tooth Abnormalities
"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
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| MeSH Number(s) |
C07.650.800 C07.793.700 C16.131.850.800
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| Concept/Terms |
Tooth Abnormalities- Tooth Abnormalities
- Abnormalities, Tooth
- Abnormality, Tooth
- Tooth Abnormality
- Teeth Abnormalities
- Abnormalities, Teeth
- Abnormality, Teeth
- Teeth Abnormality
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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 |
|---|
| 1997 | 0 | 1 | 1 | | 2001 | 1 | 0 | 1 | | 2005 | 1 | 0 | 1 | | 2006 | 0 | 1 | 1 | | 2007 | 1 | 0 | 1 | | 2015 | 1 | 0 | 1 | | 2016 | 2 | 0 | 2 | | 2017 | 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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Klein U, Paimagham B, Blumhagen R, Kroehl M, Sain J. Pyramidal and Taurodont Molars and Their Association With Other Tooth Anomalies. Pediatr Dent. 2017 Jan 15; 39(1):46-52.
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Gandhi RP, Lacy M, DeWitt P. The Association Between Gestational Age and Shape Anomalies of the Permanent Dentition. Pediatr Dent. 2016; 38(3):239-45.
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Parashar P, Preston S, Brada B, Borris T, Potter B. Rare dental manifestation in Simpson-Golabi-Behmel syndrome. Gen Dent. 2016 Jan-Feb; 64(1):e12-5.
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Ansar M, Jan A, Santos-Cortez RL, Wang X, Suliman M, Acharya A, Habib R, Abbe I, Ali G, Lee K, Smith JD, Nickerson DA, Shendure J, Bamshad MJ, Ahmad W, Leal SM. 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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Sauther ML, Cuozzo FP. Somatic variation in living, wild ring-tailed lemurs (Lemur catta). Folia Primatol (Basel). 2008; 79(2):55-78.
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Pacheco TR, Levy M, Collyer JC, de Parra NP, Parra CA, Garay M, Aprea G, Moreno S, Mancini AJ, Paller AS. Incontinentia pigmenti in male patients. J Am Acad Dermatol. 2006 Aug; 55(2):251-5.
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Maclean K, Smith J, St Heaps L, Chia N, Williams R, Peters GB, Onikul E, McCrossin T, Lehmann OJ, Adès LC. Axenfeld-Rieger malformation and distinctive facial features: Clues to a recognizable 6p25 microdeletion syndrome. Am J Med Genet A. 2005 Feb 01; 132A(4):381-5.
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Cooper SC, Flaitz CM, Johnston DA, Lee B, Hecht JT. A natural history of cleidocranial dysplasia. Am J Med Genet. 2001 Nov 15; 104(1):1-6.
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Aswegan AL, Josephson KD, Mowbray R, Pauli RM, Spritz RA, Williams MS. Autosomal dominant hypohidrotic ectodermal dysplasia in a large family. Am J Med Genet. 1997 Nov 12; 72(4):462-7.
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Chan CP, Cassingham RJ, Yukna RA, Meffert RM, Kasten FH. Morphologic and histometric characteristics of cervical enamel projections in molars of Chinese. Int J Periodontics Restorative Dent. 1988; 8(6):52-65.
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