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Molecular diagnosis of Silver-Russell Syndrome (H19 methylation and UPD7)

  • Phone : +31 (0)20 566 7899
  • Additional Phone : -
  • Fax : +31 (0)20 566 9389
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Last update: September 2009

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Uniparental disomy study
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Methylation analysis
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List of diseases and genes

List of genes tested (including panels) (1)

Quality management

EQA
 EQA

EQA scheme(s) organized by EMQN

11p-Imprinting Disorders (BWS/SRS)
2016
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.