Genetic Tests
Showing 37–48 of 106 results
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Feinnadelpunktion Schilddrüse Gen-Panel-Diagnostik
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Fetal RHD-NIPT
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Fragiles X-Syndrom (FMR1-Gen); FRAXA, Martin-Bell-Syndrom
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Gastric cancer in tumor tissue- 18 Gene; method: NGS
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Gastronintestinal stromal tumors (GIST) 8 gene: BRAF, KIT, PDGFRA, SDHA, SDHB, SDHC, SDHD, TP53 in tumor tissue
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Glioma in tumor tissue – 11 gene: ATRX, BRAF, EGFR, H3-3A, H3C2, IDH1, IDH2, PIK3CA, PTEN, TERT, TP53
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Haemochromatosis, comprehensive analysis (6 Genes: FTL, HAMP, HFE, HFE2, SLC40A1, TFR2 by NGS)
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Hämochromatose Typ 1 (HFE-Gen)
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Harmony® test – NIPT (trisomy 21,18,13 +XY chromosome + DiGeorge Syndrome (Microdeletion 22q11.2))
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Harmony® test – NIPT (trisomy 21,18,13 +XY chromosome)
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Hereditary Cancer Syndromes – Comprehensive Panel (176 genes using NGS)
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Hereditary spastic paraplegia (HSP) – 76 gene by NGS