Craniosynostosis syndromes, NGS


Identify genetic variants related to craniosynostosis; guide surgical interventions and counseling.
Genelist (92): ABCC9, ADAMTSL4, ALPL, ALX1, ALX3, ALX4, ASXL1, ATR, BMP4, BPNT2, CCBE1, CD96, CDC45, CEP120, CHST3, COLEC11, CTSK, CYP26B1, DHRS3, EDNRB, EFNA4, EFNB1, ERF, ESCO2, FAM20C, FBN1, FGF3, FGFR1, FGFR2, FGFR3, FLNA, FLNB, FREM1, GDF5, GLI3, GNAS, GNPTAB, GPC3, HUWE1, IDS, IDUA, IFT122, IFT140, IFT43, IGF1R, IHH, IL11RA, IRX5, JAG1, KAT6A, KMT2D, KRAS, LMX1B, LRP5, MASP1, MEGF8, MSX2, NOG, OSTM1, P4HB, PAX3, PHEX, POR, PRRX1, RAB23, RECQL4, RUNX2, SCARF2, SEC24D, SH3PXD2B, SIX1, SKI, SLC25A24, SMAD6, SMO, SOX10, SOX6, SOX9, SPECC1L, STAT3, TCF12, TCOF1, TGFBR1, TGFBR2, TICRR, TMCO1, TWIST1, TWIST2, WDR19, WDR35, ZEB2, ZIC1