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Pancreatitis, hereditary (NGS panel of 4 genes)
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Pancreatitis, hereditary (sequence analysis of PRSS1 gene)
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Pancreatitis, hereditary (sequence analysis of SPINK1 and PRSS1 genes)
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Pancreatitis, hereditary (sequence analysis of SPINK1 gene)
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Panel of rearrangements associated with autism (deletion/duplication analysis on 15q11-13, 16p11, 22q13 regions)
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Panel of spermatogenesis/spermiogenesis alteration (sequence analysis of AURKC and DPY19L2 genes and detection of R283Q mutation of SPATA16 gene)
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Panhypopituitarism, X-linked (sequence analysis of SOX3 gene)
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PAPA syndrome (sequence analysis of PSTPIP1 gene)
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Papillon-Lefevre syndrome |Haim-Munk syndrome| Juvenile Periodontitis 1, (sequence analysis of CTSC gene)
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Papillorenal syndrome (deletion/duplication analysis on PAX2 gene)
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Papillorenal syndrome (sequence analysis of PAX2 gene)
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Paragangliomas 1 (sequence analysis of SDHD gene)
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Paragangliomas 1,3 and 4 (deletion/duplication analysis on SDHD, SDHC and SDHB genes)
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Paragangliomas 2 (sequence analysis of SDHAF2 gene)
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Paragangliomas 3 (sequence analysis of SDHC gene)
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Paragangliomas 4 (sequence analysis of SDHB gene)
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Paragangliomas 5 (PGL5, sequence analysis of SDHA gene)
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Paragangliomas 5 and Pheochromocytoma (deletion/duplication analysis on SDHA and MAX genes)
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Paramyotonia congenita of Von Eulenburg (deletion/duplication analysis on SCN4A gene)
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Paramyotonia congenita of Von Eulenburg (sequence analysis of SCN4A gene)
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