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Kallmann(KAL1) and Steroid Sulphatase Deficiency(STS) Probe Combination Probe
- Specification
Cat.No.
FMDC-20
Description
Kallmann syndrome (KS)is a developmental disorder characterised by olfactory deficiency and hypogonadotrophic hypogonadism (HH), which is responsible for the absence of spontaneous puberty.
Steroid Sulphatase Deficiency (STS) (also known as X-linked Ichthyosis) is the second most common type of ichthyosis, and one of the most frequent human enzyme deficiency disorders.
Steroid Sulphatase Deficiency (STS) (also known as X-linked Ichthyosis) is the second most common type of ichthyosis, and one of the most frequent human enzyme deficiency disorders.
Size
5 Tests, 10 Tests
Label
Red/Green
Locus
Xp
Specificity
Human
Usage
For Research Use Only. Not for use in diagnostic procedures.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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