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Molecular diagnosis of Benign Familial Neonatal Seizures (KCNQ2 and KCNQ3 gene)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 19/11/2009
  • Phone : +31 (0)88 755 4090
  • Additional Phone : +31 (0)88 755 3800
  • Fax : +31 (0)88 755 5034
  • Website
  • Contact
Last update: November 2009

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing
Deletion / Duplication analysis
MLPA based techniques

List of diseases and genes

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