Orphanet: Diagnosi molecolare delle anomalie di chiusura del tubo neurale geni VAGNL1, VANGL2
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Molecular diagnosis of neural tube defects (VANGL1, VANGL2 genes)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 19/03/2012
  • Laboratorio di Neurogenetica
  • U.O.C. Neurologia pediatrica e Malattie muscolari
  • IRCCS Istituto G. Gaslini - Ospedale Pediatrico
  • Largo Gerolamo Gaslini 5
  • 16147 GENOVA
  • ITALY
  • Director of laboratory : -
  • More information
  • Phone : 39 010 56362603
  • Additional Phone : -
  • Fax : -
  • Website
  • Contact
Last update: March 2012

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
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List of diseases and genes

List of diseases tested (1)
Neural tube defect
List of genes tested (including panels) (2)
VANGL1
VANGL2
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