"Hemizygote" 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.
An individual having only one allele at a given locus because of the loss of the other allele through a mutation (e.g., CHROMOSOME DELETION).
Descriptor ID |
D057898
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MeSH Number(s) |
G05.380.371
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Hemizygote".
Below are MeSH descriptors whose meaning is more specific than "Hemizygote".
This graph shows the total number of publications written about "Hemizygote" by people in this website by year, and whether "Hemizygote" was a major or minor topic of these publications.
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Year | Major Topic | Minor Topic | Total |
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2011 | 0 | 1 | 1 |
2016 | 0 | 1 | 1 |
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Below are the most recent publications written about "Hemizygote" by people in Profiles.
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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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Intermittent-relapsing pyruvate dehydrogenase complex deficiency: a case with clinical, biochemical, and neuroradiological reversibility. Dev Med Child Neurol. 2012 May; 54(5):472-6.