NGS capture panel

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Showing 61–72 of 161 results

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Inflammatory bowel disease (IBD) [45 genes]

Ref.: S-202110283

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Inherited heart diseases global panel [368 genes]

Ref.: S-202313244

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Joubert syndrome [34 genes]

Ref.: S-202110429

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Klippel-Trenaunay-Weber syndrome. PIK3CA gene sequencing [1 gene]

Ref.: S-202211903

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Leber hereditary optic neuropathy. Recurrent mitochondrial genome mutations. NextGeneDx [3 genes]

Ref.: S-202212459

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Liddle syndrome (pseudohyperaldosteronism) [7 genes]

Ref.: S-202008455

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Linear nevus sebaceous syndrome. KRAS and HRAS gene sequencing [2 genes]

Ref.: S-202314153

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Maturity-onset diabetes of the young (MODY) [15 genes]

Ref.: S-202009801

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Meckel-Gruber syndrome [20 genes]

Ref.: S-202110430

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Megalencephaly – polymicrogyria – postaxial polydactyly – hydrocephalus (MPPH syndrome). PIK3CA gene sequencing [1 gene]

Ref.: S-202211832