57318-8
Chromosome 13+18+21+X+Y aneuploidy in Blood or Tissue by FISH Nominal
Active
Part Descriptions
LP62864-1 FISH
FISH (fluorescence in situ hybridization) is a cytogenetic technique used to detect and localize the presence or absence of specific DNA sequences on chromosomes. FISH uses fluorescent probes that bind to only those parts of the chromosome with which they show a high degree of sequence similarity. Fluorescence microscopy can be used to find out where the fluorescent probe bound to the chromosomes. FISH is often used for finding specific features in DNA for use in genetic counseling, medicine, and species identification. FISH can also be used to detect and localize specific mRNAs within tissue samples. In this context, it can help define the spatial-temporal patterns of gene expression within cells and tissues.
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Source: Wikipedia, FISH
LP96858-3 Chromosome 13+18+21+X+Y aneuploidy
Aneuploidy is an abnormal number of chromosomes, and is a type of chromosome abnormality. An extra or missing chromosome is a common cause of genetic disorders (birth defects). Some cancer cells also have abnormal numbers of chromosomes. Aneuploidy occurs during cell division when the chromosomes don't separate properly between the two cells. Chromosome abnormalities occur in 1 of 160 live births, the most common being extra chromosomes 21, 18 and 13.
Copyright Text is available under the Creative Commons Attribution/Share-Alike License. See http://creativecommons.org/licenses/by-sa/3.0/ for details.
Source: Wikipedia, Wikipedia
Fully-Specified Name
- Component
- Chromosome 13+18+21+X+Y aneuploidy
- Property
- Find
- Time
- Pt
- System
- Bld/Tiss
- Scale
- Nom
- Method
- FISH
Additional Names
- Short Name
- Chr 13+18+21+X+Y aneup Bld/T FISH
- Display Name
- Chr 13+18+21+X+Y aneuploidy FISH Nom (Bld/Tiss)
- Consumer Name Alpha Get Info
- Chromosome 13+18+21+X+Y aneuploidy, Blood or tissue specimen
Basic Attributes
- Class
- MOLPATH
- Type
- Laboratory
- First Released
- Version 2.29
- Last Updated
- Version 2.73
- Order vs. Observation
- Both
- Common Test Rank Get Info
- 8296
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| es-ES | Spanish (Spain) | Aneuploidía cromosoma 13+18+21+X+Y: |
| es-MX | Spanish (Mexico) | Cromosoma 13 + 18 + 21 + X + Y aneuploidía: |
| et-EE | Estonian (Estonia) | Kromosoom 13+18+21+X+Y aneuploidsus: Synonyms: Juhuslik Kude Veri Veri või koematerjal |
| fr-CA | French (Canada) | Chromosome 13+ 18+ 21+ X+ Y aneuploïdie: |
| fr-FR | French (France) | Chromosome 13+18+21+X+Y aneuploïdie: |
| it-IT | Italian (Italy) | Cromosoma 13+18+21+X+Y, aneuploidia: Synonyms: Aneuploidia del cromosoma 13+18+21+X+Y Ibridazione in situ fluorescente (FISH) Osservazione Patologia molecolare Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & |
| nl-NL | Dutch (Netherlands) | chromosoom 13+18+21+X+Y aneuploïdie: |
| pt-BR | Portuguese (Brazil) | Chromosome 13+18+21+X+Y aneuploidia: Synonyms: ; |
| tr-TR | Turkish (Turkey) | Kromozom 13+18+21+X+Y anöploidy: |
| uk-UA | Ukrainian (Ukraine) | Хромосома 13+18+21+X+Y анеуплоїдія: Synonyms: Blood; |
| zh-CN | Chinese (China) | 染色体 13+18+21+X+Y 非整倍体性: Synonyms: 13+18+21+X+Y 染色体非整倍体型; |
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