Orphanet: Diagnóstico del hiperaldosteronismo familiar tipo I gen híbrido de duplicación CYP11B1B2
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Diagnosis of familial hyperaldosteronism type 1 (CYP11B1/B2 genes, duplication hybrid gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 17/01/2017
  • Laboratorio de Diagnstico Molecular
  • Hospital Materno Infantil Gregorio Maran
  • Calle Maiquez, 9
  • 28009 MADRID
  • SPAIN
  • Director of laboratory : -
  • More information
  • Phone : 34 915 29 00 87
  • Additional Phone : -
  • Fax : 34 915 86 80 18
  • Website
Last update: January 2017

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Targeted mutation analysis
PCR based techniques

List of diseases and genes

List of diseases tested (1)
List of genes tested (including panels) (2)
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