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NGS analysis - Comprehensive panel of deafness
Gene: ABHD12, ACTG1, ADCY1, ADGRV1, AIFM1, ALMS1, ANKH, ATP2B2, ATP6V1B1, ATP6V1B2, BCAP31, BCS1L, BSND, BTD, CABP2, CACNA1D, CATSPER2, CCDC50, CD151, CDH23, CEACAM16, CEP250, CIB2, CISD2, CLDN14, CLIC5, CLPP, CLRN1, COCH, COL11A1, COL11A2, COL2A1, COL4A3, COL4A4, COL4A5, COL4A6, COL9A1, COL9A2, CRYM, DCAF17, DCDC2, DFNA5, DFNB59 , DIABLO, DIAPH1, DIAPH3, DLX5, DNMT1, DSPP, EDN3, EDNRB, ELMOD3, EPS8, ESPN, ESRRB, EYA1, EYA4, FAM65B , FGF3, FOXI1, GATA3, GFER, GIPC3, GJB2, GJB3, GJB6, GPSM2, GRHL2, GRXCR1, GRXCR2, HARS, HARS2, HGF, HOMER2, HOXA2, HOXB1, HSD17B4, CHD7, CHSY1, IGF1, ILDR1, KARS, KCNE1, KCNJ10, KCNQ1, KCNQ4, KITLG, LARS2, LHFPL5, LOXHD1, LRP2, LRTOMT, MAN2B1, MANBA, MARVELD2, MGP, MITF, MSRB3, MYH14, MYH9, MYO15A, MYO3A, MYO6, MYO7A, NARS2, NDP, NLRP3, OSBPL2, OTOA, OTOF, OTOG, OTOGL, P2RX2, PAX3, PCDH15, PDE1C, PDZD7, PEX1, PEX26, PEX6, PNPT1, POLD1, POLR1C, POLR1D, POU3F4, POU4F3, PRPS1, RDX, RMND1, RPS6KA3, SALL1, SALL4, SEMA3E, SERPINB6, SIX1, SIX5, SLC17A8, SLC19A2, SLC26A4, SLC26A5, SLC29A3, SLC33A1, SLC52A2, SLC52A3, SLITRK6, SMPX, SNAI2, SOX10, STRC, SYNE4, TBC1D24, TCOF1, TECTA, TFAP2A, TIMM8A, TMC1, TMIE, TMPRSS3, TNC, TNFRSF11B, TPRN, TRIOBP, TSHZ1, TSPEAR, TWNK, TYR, USH1C, USH1G, USH2A, WFS1, WHRN, XYLT2, YAP1
MYH9-related disease
Gene: MYH9
Kniest dysplasia
Gene: COL2A1_MLPA
Kniest dysplasia
Gene: COL2A1
DiGeorge syndrome
Gene: 22q11.2 region
Deafness, non-syndromic, DFNB
Gene: GPSM2
Deafness, non-syndromic, DFNA/DFNB
Gene: GJB6_MLPA
Deafness, non-syndromic, DFNA/DFNB
Gene: GJB2
Deafness, non-syndromic, DFNA/DFNB
Gene: GJB6
Deafness, non-syndromic, DFNA/DFNB
Gene: GJB2_MLPA
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