Chromosomes, Human, 13-15

"Chromosomes, Human, 13-15" 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.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

The medium-sized, acrocentric human chromosomes, called group D in the human chromosome classification. This group consists of chromosome pairs 13, 14, and 15.

Descriptor ID

D002901

MeSH Number(s)

A11.284.187.520.300.370

G05.360.162.520.300.370

Concept/Terms

Chromosomes, Human, 13-15

Below are MeSH descriptors whose meaning is more general than "Chromosomes, Human, 13-15".

Anatomy [A]
Cells [A11]
Cellular Structures [A11.284]
Chromosomes [A11.284.187]
Chromosomes, Mammalian [A11.284.187.520]
Chromosomes, Human [A11.284.187.520.300]
Chromosomes, Human, 13-15 [A11.284.187.520.300.370]
Biological Sciences [G]
Genetic Phenomena [G05]
Genetic Structures [G05.360]
Chromosomes [G05.360.162]
Chromosomes, Mammalian [G05.360.162.520]
Chromosomes, Human [G05.360.162.520.300]
Chromosomes, Human, 13-15 [G05.360.162.520.300.370]

Below are MeSH descriptors whose meaning is related to "Chromosomes, Human, 13-15".

Below are MeSH descriptors whose meaning is more specific than "Chromosomes, Human, 13-15".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Chromosomes, Human, 13-15" by people in Harvard Catalyst Profiles by year, and whether "Chromosomes, Human, 13-15" was a major or minor topic of these publication.

Below are the most recent publications written about "Chromosomes, Human, 13-15" by people in Profiles.

Pathogenic Yield of Genetic Testing in Autism Spectrum Disorder. Pediatrics. 2020 10; 146(4).

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Open-label use of highly purified CBD (Epidiolex®) in patients with CDKL5 deficiency disorder and Aicardi, Dup15q, and Doose syndromes. Epilepsy Behav. 2018 09; 86:131-137.

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KIT-negative gastrointestinal stromal tumors: proof of concept and therapeutic implications. Am J Surg Pathol. 2004 Jul; 28(7):889-94.

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The role of chromosomal translocation (15;19) in the carcinoma of the upper aerodigestive tract in children. Otolaryngol Head Neck Surg. 2003 Dec; 129(6):698-704.

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Recent studies of the retinoblastoma gene. What it means to the ophthalmologist. Arch Ophthalmol. 1988 Feb; 106(2):181-2.

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Cloning of the esterase D gene: a polymorphic gene probe closely linked to the retinoblastoma locus on chromosome 13. Proc Natl Acad Sci U S A. 1986 Sep; 83(17):6573-7.

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Isolation of molecular probes associated with the chromosome 15 instability in the Prader-Willi syndrome. Proc Natl Acad Sci U S A. 1986 Jun; 83(12):4408-12.

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Translocation (13;22) in a hemangiopericytoma. Cancer Genet Cytogenet. 1986 Apr 15; 21(4):309-18.

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Abnormal facial features and extremities in human trisomy syndromes: prenatal US appearance. Radiology. 1986 Apr; 159(1):243-6.

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Complexities of intraventricular abnormalities. J Pediatr. 1986 Apr; 108(4):545-51.

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