IVD RB1/RCAN1, SE X/SE Y/ SE 18

Trisomy 21 is one of the most common chromosomal abnormalities in live born children and causes Down syndrome. Trisomy 13, also called Patau syndrome, is a chromosomal condition that is associated with severe mental retardation and certain physical abnormalities. Trisomy 18 causing Edwards syndrome is the second most common autosomal trisomy after trisomy 21. The disorder/condition is characterized by severe symptoms. Turner syndrome occurs when females inherit only one X chromosome; their genotype is X0. Metafemales or triple-X females, inherit three X of more chromosomes. Klinefelter syndrome males inherit one or more extra X chromosomes; XYY syndrome males inherit an extra Y chromosome.

References:
Uchida et al, 2010, Cancer Genet Cytogenet, 203; 324-327.
Sen et al, 2002, J of Nat Canc Inst, 94; 1320-1329.
Lassmann et al, 2007, Clin Cancer Res, 13; 4083-4091.

Productos

Productos

KBI-40005
PrenatScreen (13/21 X/Y/18) 10T
Disponibilidad del país
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KBI-40006
PrenatScreen (13/21 X/Y/18) 30T
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o SOLICITE una cotización masiva.
KBI-40007
PrenatScreen (13/21 X/Y/18) 50T
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o SOLICITE una cotización masiva.

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Downloads

KBI-40005

KBI-40006

KBI-40007

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