Search Results 1-10 of 27685 for Karyotype
Chromosome analysis. Also called karyotype analysis, this test is used to confirm a diagnosis of Klinefelter syndrome. A blood sample is sent to the lab to ...
Females with this genetic disorder have three X chromosomes instead of two. Symptoms can be mild or include developmental delays and learning disabilities.
This genetic disorder occurs when a male is born with an extra copy of the X chromosome and may result in low testosterone production and infertility.
Routine Cytogenetic Analysis. Representative G-banded karyotype. Routine cytogenetic analysis by the Cytogenetics Core requires metaphase slides prepared by ...
Turner syndrome affects only females as the result of a missing or partially missing X chromosome, causing a variety of medical and developmental problems.
For example, the core can produce metaphases for cytogenetic analysis or karyotypes from an investigator's cell line of interest. In addition, the core can ...
Detecting chromosome and gene defects; Imaging and karyotyping of specimens; Reporting findings to physicians for diagnosis and treatment. Work environment.
The Cytogenetics Lab provides comprehensive testing services including chromosome analysis, probes, FISH and microarray congenital disorder assays.
... karyotype to confirm diagnosis. Using a sample of blood, this test analyzes your child's chromosomes. If there's an extra chromosome 21 in all or some cells ...
However, doing a karyotype during pregnancy or after delivery is recommended to confirm the diagnosis. If Turner syndrome is suspected before birth ...
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