"Genes, X-Linked" 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.
Genes that are located on the X CHROMOSOME.
Descriptor ID |
D050172
|
MeSH Number(s) |
G05.360.340.024.340.500 G05.420.457
|
Concept/Terms |
Genes, X-Linked- Genes, X-Linked
- Genes, X Linked
- Genes, X-Chromosome
- Gene, X-Chromosome
- Genes, X Chromosome
- X-Chromosome Gene
- X-Chromosome Genes
- X Chromosome Genes
- X-Linked Genes
- Gene, X-Linked
- X Linked Genes
- X-Linked Gene
Alleles, X-Linked- Alleles, X-Linked
- Allele, X-Linked
- Alleles, X Linked
- X-Linked Allele
- X-Linked Alleles
X-Linked Traits- X-Linked Traits
- Trait, X-Linked
- X Linked Traits
- X-Linked Trait
- Traits, X-Linked
- Traits, X Linked
|
Below are MeSH descriptors whose meaning is more general than "Genes, X-Linked".
Below are MeSH descriptors whose meaning is more specific than "Genes, X-Linked".
This graph shows the total number of publications written about "Genes, X-Linked" by people in this website by year, and whether "Genes, X-Linked" 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 |
---|
2009 | 0 | 1 | 1 |
2013 | 1 | 0 | 1 |
2015 | 1 | 0 | 1 |
2016 | 1 | 1 | 2 |
2020 | 0 | 1 | 1 |
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click here.
Below are the most recent publications written about "Genes, X-Linked" by people in Profiles.
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Defining the genotypic and phenotypic spectrum of X-linked MSL3-related disorder. Genet Med. 2021 02; 23(2):384-395.
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Mutation Update for Kabuki Syndrome Genes KMT2D and KDM6A and Further Delineation of X-Linked Kabuki Syndrome Subtype 2. Hum Mutat. 2016 09; 37(9):847-64.
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X-linked recessive VACTERL-H due to a mutation in FANCB in a preterm boy. Clin Dysmorphol. 2016 Apr; 25(2):73-6.
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Tentative clinical diagnosis of Lujan-Fryns syndrome--A conglomeration of different genetic entities? Am J Med Genet A. 2016 Jan; 170A(1):94-102.
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Do not trust the pedigree: reduced and sex-dependent penetrance at a novel mutation hotspot in ATL1 blurs autosomal dominant inheritance of spastic paraplegia. Hum Mutat. 2013 Jun; 34(6):860-3.
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Goltz-Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap. Eur J Hum Genet. 2009 Oct; 17(10):1207-15.