Orphanet: Diagnóstico del cáncer de colon no polipósico genes MLH1, MSH2, MSH6 y PMS2
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Diagnosis of familial nonpolyposis colon cancer (MLH1, MSH2, MSH6 and PMS2 genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 15/06/2017
  • Laboratorio de gentica molecular y citogentica
  • Centro de Bioqumica y Gentica Clnica
  • Carretera Cartagena-Madrid s/n
  • 30120 EL PALMAR
  • SPAIN
  • Director of laboratory : Dr Isabel LPEZ-EXPSITO
  • More information
  • Phone : 34 96 838 11 66
  • Additional Phone : 34 96 838 12 29
  • Fax : 34 96 838 12 22
  • Website
Last update: June 2017

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing
Sequence analysis: entire coding region
NGS sequencing (except WES)
Deletion / Duplication analysis
MLPA based techniques

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (4)

Quality management

EQA
 EQA

EQA scheme(s) organized by EMQN

HNPCC (Hereditary non-polyposis colon cancer)
2015, 2016, 2017, 2018, 2019
The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.