Hybridization of the RCAN1 (21q22), SE X, SE Y probe to a male metaphase spread showing normal pattern (2R1G1B)

IVD RCAN1/SE X/SE Y

ivd-rcan1-se-x-se-y
Chromosomal abnormalities involving the X and Y chromosome (sex chromosomes) are slightly less common than autosomal abnormalities and are usually much less severe in their effects. The high frequency of people with sex chromosome aberrations is partly due to the fact that they are rarely lethal conditions.
- Turner syndrome occurs when females inherit only one X chromosome - their genotype is X0.
- Metafemales or triple-X females, inherit three X chromosomes - their genotype is XXX or more rarely XXXX or XXXXX.
- Klinefelter syndrome males inherit one or more extra X chromosomes - their genotype is XXY or more rarely XXXY, XXXXY, or XY/XXY mosaic.
  • KBI-40008
    Checar Disponibilidade
    PloidyScreen (21 X Y) 20T
  • KBI-45008
    Checar Disponibilidade
    Ploidy screen (2 1 / X / Y )

Especificaç÷es de Produtos

Especificaç÷es de Produtos

KBI-40008
Prenatal
In Vitro Diagnostic Use
20 test
Triple Color > Red, Blue, Green
Cells
Trisomy
Gene Region-Specific
Fluorescent
Ready-to-Use
Manual Reagent
KBI-45008
Prenatal
In Vitro Diagnostic Use
5 test
Triple Color > Red, Blue, Green
Cells
Trisomy
Gene Region-Specific
Fluorescent
Ready-to-Use
Manual Reagent

Documentos

Documentos

Recursos

Recursos

Chromosomal abnormalities involving the X and Y chromosome (sex chromosomes) are slightly less common than autosomal abnormalities and are usually much less severe in their effects. The high frequency of people with sex chromosome aberrations is partly due to the fact that they are rarely lethal conditions.
- Turner syndrome occurs when females inherit only one X chromosome - their genotype is X0.
- Metafemales or triple-X females, inherit three X chromosomes - their genotype is XXX or more rarely XXXX or XXXXX.
- Klinefelter syndrome males inherit one or more extra X chromosomes - their genotype is XXY or more rarely XXXY, XXXXY, or XY/XXY mosaic.

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