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One single mix for testing of six relevant risk factors for thrombophilia.
Kit enabling the simultaneous detection of the 3 most frequent mutations and the corresponding WT variants in the HFE gene.
NGS kit for the identification of 12 SNPs in polygenic FH & the 6 SNPs to predict statin response.
Detection of SNV, InDel and CNV germline mutations for a wide range of cardiac and metabolic diseases by NGS.