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Hot Products
Kallmann(KAL1) and Steroid Sulphatase Deficiency(STS) Probe Combination Probe
- Specification
- Q & A
- Customer Review
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
Specificity
Human
Locus
Xp
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.
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