Requisition required.
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Bardet-Biedl Syndrome
Heterotaxias
Joubert Syndrome
Meckel-Gruber Syndrome
Nephronophthisis
Orofaciodigital Syndrome Type 1
Primary Ciliary Dysfunction
Senior-Loken Syndrome
GPR98, TSC1, TSC2, IFT43, WDR19, WDR35, ACVR2B, CITED2, CRELD1, DNAH11, DNAH5, DNAI1, GATA4, GDF1, LEFTY2, NKX2-5, SHROOM3, SMAD2, ZIC3, AIPL1, ARL6, ATXN10, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, C2orf71, C5orf42, CCDC28B, CCDC39, CCDC40, CDH23, CFTR, CLRN1, CRB1, CRX, DFNB31, DNAAF1, DNAAF2, DNAAF3, DNAI2, DNAL1, DYNC2H1, EVC, EVC2, GLIS2, GUCY2D, HYLS1, IFT80, IMPDH1, INVS, IQCB1, KCNJ13, LCA5, LRAT, MKKS, MYO7A, NEK1, NEK8, NME8, NPHP4, PCDH15, PKD2, PKHD1, RD3, RDH12, RPE65, RPGR, RPGRIP1, RSPH4A, RSPH9, SCNN1A, SCNN1B, SCNN1G, SDCCAG8, SPATA7, TOPORS, TTC8, TULP1, UMOD, USH1C, USH1G, USH2A, VHL, WDPCP, XPNPEP3, TRIM32, FOXH1, NODAL, AHI1, ARL13B, B9D1, B9D2, CC2D2A, CEP290, CEP41, INPP5E, KIF7, MKS1, NPHP1, NPHP3, OFD1, RPGRIP1L, TCTN1, TCTN2, TMEM138, TMEM216, TMEM237, TMEM67, TTC21B