• Dilate Kardiyomiyopati (Panel)

    ABCC9, ACTC1, ACTN2, ANKRD1, BAG3, CRYAB, CSRP3, DES, DMD, DNAJC19, DOLK, DSC2, DSG2, DSP, EMD, EYA4, FKTN, GATA4, GATAD1, ILK, LAMA4, LAMP2, LDB3, LMNA, MURC, MYBPC3, MYH6, MYH7, MYPN, NEBL, NEXN, PDLIM3, PKP2, PLN, PRDM16, RAF1, RBM20, SCN5A, SGCD, TAZ, TBX20, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, TXNRD2, VCL


    Dilate Kardiyomiyopati (Delesyon&Duplikasyon)

    MYBPC3, TNNT2, SGCD, MYH7, RAF1, BAG3, DMD, DSC2, DSG2, SCN5A, LMNA, PKP2, FKTN, DSP, GATA4


    Dejerin-Sottas Sendromu (Panel)

    MPZ, PMP22, PRX, EGR2, GJB1


    Diamond-Blackfan Anemisi (Panel)

    GATA1, RPL11, RPL15, RPL26, RPL27, RPL31, RPL35A, RPL5, RPS10, RPS17, RPS19, RPS24, RPS26, RPS27, RPS28, RPS29, RPS7, TSR2


    Diamond-Blackfan Anemisi (Delesyon&Duplikasyon)

    RPL35A, RPS17, RPL11, RPL5, RPS26, RPS19


    Dolikoektazi (Panel)

    COL4A1, COL4A2, GAA, MMP3, PKD1, PKD2, SLC2A10


    Dravet Sendromu (Panel)

    SCN1A, GABRG2, SCN2A, SCN9A


    Distrofik Olmayan Miyotoni Congenita (Panel)

    ATP2A1, CACNA1S, CAV3, CLCN1, HINT1, HSPG2, KCNA1, KCNE3, SCN4A


    Dopa Yanıtlı Distoni (Yeni Nesil Dizileme Paneli ve Kopya Sayısı Varyasyon Analizi; 5 Gen)

    GCH1 (600225), QDPR (612676), SLC6A3 (126455), SPR (182125), TH (191290).


    Dopamine Metabolism Deficiency (NextGen Sequencing Panel and Copy Number Analysis; 13 Genes)

    COMT (116790), DBH (609312), DDC (107930), DRD3 (126451), DRD4 (126452), DRD5 (126453), GCH1 (600225), MAOA (309850), PTS (612719), QDPR (612676), SLC6A3 (126455), SPR (182125), TH (191290).