"Chromosome Disorders" 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.
Clinical conditions caused by an abnormal chromosome constitution in which there is extra or missing chromosome material (either a whole chromosome or a chromosome segment). (from Thompson et al., Genetics in Medicine, 5th ed, p429)
| Descriptor ID |
D025063
|
| MeSH Number(s) |
C16.131.260 C16.320.180
|
| Concept/Terms |
Chromosome Disorders- Chromosome Disorders
- Chromosome Disorder
- Disorder, Chromosome
- Disorders, Chromosome
- Chromosome Abnormality Disorders
- Chromosome Abnormality Disorder
- Disorder, Chromosome Abnormality
- Chromosomal Disorders
- Chromosomal Disorder
- Disorder, Chromosomal
- Disorders, Chromosomal
Autosomal Chromosome Disorders- Autosomal Chromosome Disorders
- Autosomal Chromosome Disorder
- Chromosome Disorder, Autosomal
- Chromosome Disorders, Autosomal
|
Below are MeSH descriptors whose meaning is more general than "Chromosome Disorders".
Below are MeSH descriptors whose meaning is more specific than "Chromosome Disorders".
This graph shows the total number of publications written about "Chromosome Disorders" by people in this website by year, and whether "Chromosome Disorders" 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 |
|---|
| 2015 | 1 | 0 | 1 |
| 2017 | 4 | 2 | 6 |
| 2018 | 10 | 1 | 11 |
| 2019 | 1 | 0 | 1 |
To return to the timeline, click here.
Below are the most recent publications written about "Chromosome Disorders" by people in Profiles.
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Advantages of Array Comparative Genomic Hybridization Using Buccal Swab DNA for Detecting Pallister-Killian Syndrome. Ann Lab Med. 2019 Mar; 39(2):232-234.
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Tetrasomy 18p: The challenges of noninvasive prenatal testing and combined test. J Obstet Gynaecol Res. 2019 Mar; 45(3):705-708.
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Retrospective analysis of indications for termination of pregnancy. J Obstet Gynaecol. 2019 Apr; 39(3):355-358.
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Variability in Phelan-McDermid syndrome: The impact of the PNPLA3 p.I148M polymorphism. Clin Genet. 2018 12; 94(6):590-591.
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Update in non-invasive prenatal testing. Minerva Ginecol. 2019 Feb; 71(1):44-53.
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Prospective observations study protocol to investigate cost-effectiveness of various prenatal test strategies after the introduction of noninvasive prenatal testing. BMC Pregnancy Childbirth. 2018 Jul 24; 18(1):307.
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Mayer-Rokitansky-Küster-Hauser Syndrome and 16p11.2 Recurrent Microdeletion: A Case Report and Review of the Literature. J Pediatr Adolesc Gynecol. 2018 Oct; 31(5):533-535.
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[Application of single nucleotide polymorphism microarray and fluorescence in situ hybridization analysis for the prenatal diagnosis of a case with Pallister-Killian syndrome]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2018 Apr 10; 35(2):232-235.
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Pregnancy Outcomes after ZIKV Infection in French Territories in the Americas. N Engl J Med. 2018 03 15; 378(11):985-994.
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Otud7a Knockout Mice Recapitulate Many Neurological Features of 15q13.3 Microdeletion Syndrome. Am J Hum Genet. 2018 02 01; 102(2):296-308.