"Skull" 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.
The SKELETON of the HEAD including the FACIAL BONES and the bones enclosing the BRAIN.
Descriptor ID |
D012886
|
MeSH Number(s) |
A02.835.232.781
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Skull".
Below are MeSH descriptors whose meaning is more specific than "Skull".
This graph shows the total number of publications written about "Skull" by people in this website by year, and whether "Skull" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1995 | 0 | 1 | 1 |
2007 | 0 | 1 | 1 |
2009 | 1 | 0 | 1 |
2010 | 1 | 1 | 2 |
2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Skull" by people in Profiles.
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p63 establishes epithelial enhancers at critical craniofacial development genes. Sci Adv. 2019 05; 5(5):eaaw0946.
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Copy-number variations involving the IHH locus are associated with syndactyly and craniosynostosis. Am J Hum Genet. 2011 Jan 07; 88(1):70-5.
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Comparative cranial osteology of fossorial lizards from the tribe Gymnophthalmini (Squamata, Gymnophthalmidae). J Morphol. 2010 Nov; 271(11):1352-65.
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Two adults with Rubinstein-Taybi syndrome with mild mental retardation, glaucoma, normal growth and skull circumference, and camptodactyly of third fingers. Am J Med Genet A. 2009 Dec; 149A(12):2849-54.
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Esophageal atresia, hypoplasia of zygomatic complex, microcephaly, cup-shaped ears, congenital heart defect, and mental retardation--new MCA/MR syndrome in two affected sibs and a mildly affected mother? Am J Med Genet A. 2007 Jun 01; 143A(11):1135-42.
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A nine-month-old boy with microcephaly, cataracts, intracerebral calcifications and dysmorphic signs: an additional observation of an autosomal recessive congenital infection-like syndrome? Genet Couns. 1995; 6(4):297-302.