Next Generation Sequencing of 6 gene panel: FGF9, FLNB, GDF5, HOXA11, NOG, TTR.

Consult

Documentation:
Ref: LV2244 Categories: , , , , , , , Diseases: Defects in joint formation and synostoses: Multiple synostoses syndrome type 1, 2, 3. Proximal symphalangism type 1, 2. Radio-ulnar synostosis with amegakaryocytic thrombGenes: HOXA11, FGF9, TTR, GDF5, FLNB, NOGDelivery term: 42 days
sistemas genómicos
Privacy Summary

This website uses cookies so that we can offer you the best possible user experience. Cookie information is stored in your browser and performs functions such as recognizing you when you return to our website or helping our team understand which sections of the website you find most interesting and useful. You can access our privacy policy here