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Molecular diagnosis of Hereditary Persistence of Fetal Haemoglobin - HPFH (HBB, HBD, HBG1 and HBG2 genes: Prenatal diagnosis by sequencing of the entire coding region of gene (s) plus copy number analysis / postnatal by Sequencing of selected exons / targetted mutation analysis)

Despite our efforts to ensure that data is up to date, this activity has not been validated since 13/09/2017
  • The Red Cell Centre (Special Haematology Department)
  • KingsPath Clinical Diagnostic Pathology Services
  • King's College Hospital
  • Denmark Hill
  • Director of laboratory : Dr Barnaby CLARK
  • More information
  • Phone : 44 (0)203 299 9000
  • Additional Phone : 44 (0) 20 3299 1246 / 2265
  • Fax : -
  • Website
  • Contact
Last update: September 2017

Responsible of diagnostic test


Antenatal diagnosis
Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Targeted mutation analysis
MLPA based techniques
Targeted mutation analysis
NGS sequencing (except WES)
Targeted mutation analysis
PCR based techniques

List of diseases and genes

List of genes tested (including panels) (3)
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.