Karyotype - National Human Genome Research Institute
A karyotype is an individual’s complete set of chromosomes. The term also refers to a laboratory-produced image of a person’s chromosomes isolated from an individual cell and arranged in numerical order. A karyotype may be used to look for abnormalities in chromosome number or structure.

Karyotype | Description, Chromosome Aberration, & Uses | Britannica
karyotype, visual representation of the complete set of chromosomes in a cell. In a karyotype, the chromosomes, isolated from a cell, are organized numerically, facilitating the identification of deviations in chromosome number or structure.

Karyotype Test: Test & What Is It - Cleveland Clinic
A karyotype test examines blood or body fluids for abnormal chromosomes. Adults, children or developing fetuses may need this test if they’re at risk for certain genetic conditions. Before choosing to have a karyotype test, talk with your healthcare provider about genetic counseling.

Karotyoping: What It Can Reveal and How It's Done - Verywell Health
A karyotype is, quite literally, a photograph of the chromosomes that exist within a cell. A healthcare provider may order a karyotype during pregnancy to screen for common congenital defects. It is also sometimes used to help confirm a leukemia diagnosis.

Karyotype - Wikipedia
A karyotype is the general appearance of the complete set of chromosomes in the cells of a species or in an individual organism, mainly including their sizes, numbers, and shapes.

Make a Karyotype - University of Utah
A karyotype is an organized profile of a person's chromosomes. Two chromosomes specify sex, XX for female and XY for male. The rest are arranged in pairs, numbered 1 through 22, from largest to smallest.

Karyotype – IMGC Education Module
A karyotype is a visual representation of the chromosomes within a single cell. A karyotype can detect large chromosomal differences. In this section, we explain how a karyotype works and the different types of results.

Genetics, Cytogenetic Testing And Conventional Karyotype
This review explains the types of chromosome analysis, such as karyotyping, fluorescence in situ hybridization (FISH), and chromosomal microarray analysis (CMA). Go to: Specimen collection modalities include fine-needle aspiration cytology, fluid sampling and centrifugation, and tissue sampling.

Karyotype Genetic Test - MedlinePlus
A karyotype test looks for abnormal chromosomes in your cells. This test can be used prenatally to help find genetic disorders in unborn babies. Learn more.

Karyotyping: Overview, Procedure, and Risks - Healthline
Karyotyping is a laboratory procedure that allows your doctor to examine your set of chromosomes. “Karyotype” also refers to the actual collection of chromosomes being examined.