Craniofacial Abnormalities
"Craniofacial 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 structural deformities, malformations, or other abnormalities of the cranium and facial bones.
Descriptor ID |
D019465
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MeSH Number(s) |
C05.660.207 C16.131.621.207
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Craniofacial Abnormalities".
Below are MeSH descriptors whose meaning is more specific than "Craniofacial Abnormalities".
This graph shows the total number of publications written about "Craniofacial Abnormalities" by people in this website by year, and whether "Craniofacial Abnormalities" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2004 | 1 | 0 | 1 |
2011 | 0 | 1 | 1 |
2016 | 1 | 0 | 1 |
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Below are the most recent publications written about "Craniofacial Abnormalities" by people in Profiles.
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Anthropometrically-Based Surgical Technique for Tessier 3 Cleft Reconstruction. J Craniofac Surg. 2016 Nov; 27(8):e785-e787.
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Characteristics of dental clinics in US children's hospitals. Pediatr Dent. 2011 Mar-Apr; 33(2):100-6.
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Ring chromosome 9 [r(9)(p24q34)]: a report of two cases. Am J Med Genet A. 2005 Oct 15; 138A(3):229-35.
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A new genomic duplication syndrome complementary to the velocardiofacial (22q11 deletion) syndrome. Clin Genet. 2004 May; 65(5):400-4.
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Loss of the Max-interacting protein Mnt in mice results in decreased viability, defective embryonic growth and craniofacial defects: relevance to Miller-Dieker syndrome. Hum Mol Genet. 2004 May 15; 13(10):1057-67.
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The floating harbor syndrome with cardiac septal defect. Am J Med Genet. 1996 Dec 18; 66(3):300-2.