Cri-Du-Chat CTNND2 (5p15) / 5q31 probe hybridized to a normal metaphase 2RG).

IVD CTNND2

ivd-ctnnd2
Cri-Du-Chat syndrome is an autosomal deletion syndrome caused by a partial deletion of chromosome 5p. It is characterized by a distinctive, high-pitched, catlike cry in infancy with growth failure, microcephaly, facial abnormalities, and mental retardation throughout life. Loss of a small region in band 5p15.2 (Cri-Du-Chat critical region) correlates with all the clinical features of the syndrome with the exception of the catlike cry, which maps to band 5p15.3 (catlike cry critical region). The Cri-Du-Chat region probe is optimized to detect copy numbers at the CTNND2 gene region in the Cri-Du-Chat critical region at 5p15.2. The 5q31 specific FISH probe is included as control probe.

References:
Overhauser et al, 1994, Hum. Mol. Genet., 3; 247-252.
Gersh et al, 1997, Cytogenet Cell Genet., 77; 246-251.

Products

Products

KBI-40106
MD Cri-Du-Chat CTNND (5p15) / 5q31 10T
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Constitutional
In Vitro Diagnostic Use
100 µL
Dual Color > Red, Green
Cells
Deletion
Gene Region-Specific
Fluorescent
Ready-to-Use
Manual Reagent
KBI-45106
MD Cri-Du-Chat CTNND (5p15) / 5q31 5T
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Constitutional
In Vitro Diagnostic Use
50 µL
Dual Color > Red, Green
Cells
Deletion
Gene Region-Specific
Fluorescent
Ready-to-Use
Manual Reagent

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