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Diagnosis of congenital secondary polycythemia (EGLN1, EPAS1, VHL genes)

  • Phone : 49 (0)40 53805 853
  • Additional Phone : -
  • Fax : 49 (0)40 53805 821
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Last update: November 2019

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
Sanger sequencing

List of diseases and genes

List of genes tested (including panels) (3)

Additional information

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.