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Prader-Willi/Angelman(SNRPN) Probe
- Specification
Cat.No.
FMDC-33
Description
Prader-Willi Syndrome (PWS) and Angelman Syndrome (AS) are distinct neurogenetic disorders caused by the loss of function of genes on chromosome 15 (bands 15q11-13), on either the paternally or maternally inherited chromosome respectively.
Size
5 Tests, 10 Tests
Label
Red/Green
Specificity
Human
Locus
15q11-13
Usage

Storage
Store at minus 20 centigrade
Citation Guidance
If you use this products in your scientific publication, it should be cited in the publication as: Creative Bioarray cat no. If your paper has been published, please click here to submit the PubMed ID of your paper to get a coupon.
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