Cytogenetics: Difference between revisions
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{{ | {{Definitions | ||
|Short definition=cytogenetic analysis - {{ | |Term=cytogenetics | ||
|Type= | |Short definition=cytogenetic analysis - {{Pronunciation}} (SY-toh-jeh-NEH-tik uh-NA-lih-sis) The process of analyzing cells in a sample of tissue, blood, bone marrow, or amniotic fluid to look for changes in chromosomes, including broken, missing, rearranged, or extra chromosomes. Changes in certain chromosomes can be a sign of a genetic disease or condition, or some types of cancer. | ||
|Type=Cancer terms | |||
|Specialty=Oncology | |||
|Language=English | |||
|Source=NCI | |||
}} | }} | ||
cytogenetics - {{Pronunciation}} (SY-toh-jeh-NEH-tix) The study of chromosomes, which are long strands of DNA and protein that contain most of the genetic information in a cell. Cytogenetics involves testing tissue, blood, or bone marrow samples in a laboratory to look for changes in chromosomes, including broken, missing, rearranged, or extra chromosomes. Changes in certain chromosomes can be a sign of a genetic disease or condition, or some types of cancer. Cytogenetics can be used to diagnose a disease or condition, plan for treatment, or find out how well treatment is working {{dictionary-stub}} [[Category:Dictionary of medicine]] | |||
Revision as of 15:05, 8 January 2023
| Cytogenetics | |
|---|---|
| Term | Cytogenetics |
| Short definition | cytogenetic analysis - (pronounced) (SY-toh-jeh-NEH-tik uh-NA-lih-sis) The process of analyzing cells in a sample of tissue, blood, bone marrow, or amniotic fluid to look for changes in chromosomes, including broken, missing, rearranged, or extra chromosomes. Changes in certain chromosomes can be a sign of a genetic disease or condition, or some types of cancer. |
| Type | Cancer terms |
| Specialty | Oncology |
| Language | English |
| Source | NCI |
| Comments | |
cytogenetics - (pronounced) (SY-toh-jeh-NEH-tix) The study of chromosomes, which are long strands of DNA and protein that contain most of the genetic information in a cell. Cytogenetics involves testing tissue, blood, or bone marrow samples in a laboratory to look for changes in chromosomes, including broken, missing, rearranged, or extra chromosomes. Changes in certain chromosomes can be a sign of a genetic disease or condition, or some types of cancer. Cytogenetics can be used to diagnose a disease or condition, plan for treatment, or find out how well treatment is working
External links
- Medical encyclopedia article on Cytogenetics
- Wikipedia's article - Cytogenetics
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