"Chromosome Banding" 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.
Staining of bands, or chromosome segments, allowing the precise identification of individual chromosomes or parts of chromosomes. Applications include the determination of chromosome rearrangements in malformation syndromes and cancer, the chemistry of chromosome segments, chromosome changes during evolution, and, in conjunction with cell hybridization studies, chromosome mapping.
| Descriptor ID |
D002871
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| MeSH Number(s) |
E01.370.225.500.385.130 E01.370.225.500.620.670.130 E01.370.225.750.600.670.130 E05.200.500.385.130 E05.200.500.620.670.130 E05.200.750.600.670.130 E05.242.385.130 E05.393.285.130
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| Concept/Terms |
Chromosome Banding- Chromosome Banding
- Banding, Chromosome
- Bandings, Chromosome
- Chromosome Bandings
|
Below are MeSH descriptors whose meaning is more general than "Chromosome Banding".
Below are MeSH descriptors whose meaning is more specific than "Chromosome Banding".
This graph shows the total number of publications written about "Chromosome Banding" by people in this website by year, and whether "Chromosome Banding" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2001 | 0 | 1 | 1 |
| 2002 | 0 | 2 | 2 |
| 2007 | 0 | 1 | 1 |
| 2011 | 0 | 1 | 1 |
| 2017 | 0 | 1 | 1 |
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Below are the most recent publications written about "Chromosome Banding" by people in Profiles.
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Hurd LM, Thacker MM, Okenfuss E, Duker AL, Lou Y, Harty MP, Conard K, Lian JB, Bober MB. Aneurysmal bone cysts and pathologic fracture associated with supernumerary ring chromosome 6 in two unrelated patients. Am J Med Genet A. 2017 Dec; 173(12):3205-3210.
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Li P, Pomianowski P, DiMaio MS, Florio JR, Rossi MR, Xiang B, Xu F, Yang H, Geng Q, Xie J, Mahoney MJ. Genomic characterization of prenatally detected chromosomal structural abnormalities using oligonucleotide array comparative genomic hybridization. Am J Med Genet A. 2011 Jul; 155A(7):1605-15.
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Kowalski J, Morsberger LA, Blackford A, Hawkins A, Yeo CJ, Hruban RH, Griffin CA. Chromosomal abnormalities of adenocarcinoma of the pancreas: identifying early and late changes. Cancer Genet Cytogenet. 2007 Oct 1; 178(1):26-35.
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Huang T, Lin AE, Cox GF, Golden WL, Feldman GL, Ute M, Schrander-Stumpel C, Kamisago M, Vermeulen SJ. Cardiac phenotypes in chromosome 4q- syndrome with and without a deletion of the dHAND gene. Genet Med. 2002 Nov-Dec; 4(6):464-7.
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de Chadar?vian JP, Dunn S, Malatack JJ, Ganguly A, Blecker U, Punnett HH. Chromosome rearrangement with no apparent gene mutation in familial adenomatous polyposis and hepatocellular neoplasia. Pediatr Dev Pathol. 2002 Jan-Feb; 5(1):69-75.
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Martin-DeLeon PA, Piumi F, Canaff L, Rogel-Gaillard C, Hendy GN. Assignment of the parathyroid hormone/parathyroid hormone-related peptide receptor (PTHR1) to rabbit chromosome band 9p14-->p13 by fluorescence in situ hybridization. Cytogenet Cell Genet. 2001; 94(1-2):90-1.
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Iolascon A, Parrella T, Perrotta S, Guardamagna O, Coates PM, Sartore M, Surrey S, Fortina P. Rapid detection of medium chain acyl-CoA dehydrogenase gene mutations by non-radioactive, single strand conformation polymorphism minigels. J Med Genet. 1994 Jul; 31(7):551-4.