Limb Deformities, Congenital
"Limb Deformities, Congenital" 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 of the upper and lower extremities collectively or unspecified.
Descriptor ID |
D017880
|
MeSH Number(s) |
C05.660.585 C16.131.621.585
|
Concept/Terms |
Limb Deformities, Congenital- Limb Deformities, Congenital
- Congenital Limb Deformities
- Congenital Limb Deformity
- Deformities, Congenital Limb
- Deformity, Congenital Limb
- Limb Deformity, Congenital
|
Below are MeSH descriptors whose meaning is more general than "Limb Deformities, Congenital".
Below are MeSH descriptors whose meaning is more specific than "Limb Deformities, Congenital".
This graph shows the total number of publications written about "Limb Deformities, Congenital" by people in this website by year, and whether "Limb Deformities, Congenital" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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1995 | 1 | 0 | 1 |
1996 | 1 | 1 | 2 |
1999 | 1 | 2 | 3 |
2003 | 1 | 0 | 1 |
2009 | 0 | 1 | 1 |
2017 | 0 | 1 | 1 |
2019 | 1 | 0 | 1 |
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Below are the most recent publications written about "Limb Deformities, Congenital" by people in Profiles.
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VACTERL Association with Situs Inversus Totalis: A Unique Combination. Neonatal Netw. 2019 Mar 01; 38(2):98-106.
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A Recurrent De Novo Nonsense Variant in ZSWIM6 Results in Severe Intellectual Disability without Frontonasal or Limb Malformations. Am J Hum Genet. 2017 Dec 07; 101(6):995-1005.
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Conditional inactivation of Has2 reveals a crucial role for hyaluronan in skeletal growth, patterning, chondrocyte maturation and joint formation in the developing limb. Development. 2009 Aug; 136(16):2825-35.
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Role of environmental pollutants on immune functions, parasitic infections and limb malformations in marine toads and whistling frogs from Bermuda. Int J Environ Health Res. 2003 Jun; 13(2):125-48.
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Targeted disruption of Hoxd9 and Hoxd10 alters locomotor behavior, vertebral identity, and peripheral nervous system development. Dev Biol. 1999 Dec 15; 216(2):595-610.
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Interpretation of radiographs in a pediatric limb deformity practice: do radiologists contribute? J Pediatr Orthop. 1999 Nov-Dec; 19(6):732-4.
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Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice. Hum Mol Genet. 1999 Aug; 8(8):1579-84.
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A new Seckel-like syndrome of primordial dwarfism. Am J Med Genet. 1996 Aug 23; 64(3):447-52.
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Genetic analysis of the retinoid signal. Ann N Y Acad Sci. 1996 Jun 08; 785:12-22.
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Mouse embryos lacking RXR alpha are resistant to retinoic-acid-induced limb defects. Development. 1995 Dec; 121(12):3997-4003.