Orphanet: Diagnóstico del síndrome de Lynch panel
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Diagnosis of Lynch syndrome (panel)

  • Phone : 34 966 616 185
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Last update: March 2020

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Targeted mutation analysis
NGS sequencing (except WES)
Mutation scanning/screening and sequence analysis of selected exons
NGS sequencing (except WES)
Sequence analysis: entire coding region
NGS sequencing (except WES)

List of diseases and genes

List of genes tested (including panels) (7)

Additional information

Quality management

EQA
 EQA

EQA scheme(s) organized by EMQN

HNPCC (Hereditary non-polyposis colon cancer)
2015, 2016, 2017, 2018, 2019
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