Next Generation Sequencing of 4 gene panel: IL11RA, MSX2, RECQL4, TWIST1.

Consult

Documentation:
Ref: LV2235 Categories: , , , , , , , Diseases: Craniosynostosis syndromes: Baller-Gerold syndrome, Robinow-Sorauf syndrome, Saethre-Chotzen syndrome with eyelid anomalies, Saethre-Chotzen syndrome, Pfeiffer 1 syndrome, Craniosynostosis BoGenes: MSX2, TWIST1, IL11RA, RECQL4Delivery term: 42 days