1. Mendelian
  2. Experts
  3. PRADER-WILLI SYNDROME DUE TO IMPRINTING MUTATION Experts by country

PRADER-WILLI SYNDROME DUE TO IMPRINTING MUTATION Experts

We have collected the completed list of expert related to PRADER-WILLI SYNDROME DUE TO IMPRINTING MUTATION using public data available on different databases.

PRADER-WILLI SYNDROME DUE TO IMPRINTING MUTATION Experts map



If you find this map or researchers for PRADER-WILLI SYNDROME DUE TO IMPRINTING MUTATION useful, maybe you will be also interested in other rare diseases proffesionals like our leber congenital amaurosis expert list ,or our retinopathy of prematurity expert list

PRADER-WILLI SYNDROME DUE TO IMPRINTING MUTATION Experts list

Pr Bernhard HORSTHEMKE

 ESSEN. GERMANY

  Coordinator of expert centre - Clinical expert - Clinical geneticist - Responsible for diagnostic tests - Investigator of research project - Coordinator of research network - Director of laboratory

  • Research area/topic:
    Network for imprinting diseases: clinical spectrum and pathogenic mechanisms (coordination)
  • Universitätsklinikum Essen
    Universitätsklinikum Essen
Complete Info

Pr Reiner SIEBERT

 ULM. GERMANY

  Clinical expert - Clinical geneticist - Investigator of research project - Coordinator of research network - Director of department

  • Research area/topic:
    Network for imprinting diseases: Multilocus imprint mistakes, TNDM and iPS cells for imprinting diseases
  • Universitätsklinikum Ulm
  • reiner.*******@***_ulm.de
Complete Info

Dr Guiomar PEREZ DE NANCLARES LEAL

 HUÉRCAL-OVERA. SPAIN

  Responsible for diagnostic tests - Investigator of research project - Contact person of patient organisation - Director of laboratory

  • Research area/topic:
    Imprinting disorders: low grade mosaicism or new candidate genes? - ES
  • Unidad de Investigación, HUA - Hospital Universitario Araba. Sede Txagorritxu
    Asociación Española de PHP
  • gnanc*****@***kidetza.eus
Complete Info

Dr Guiomar PEREZ DE NANCLARES LEAL

 VITORIA-GASTEIZ. SPAIN

  Responsible for diagnostic tests - Investigator of research project - Contact person of patient organisation - Director of laboratory

  • Research area/topic:
    Imprinting disorders: low grade mosaicism or new candidate genes? - ES
  • Unidad de Investigación, HUA - Hospital Universitario Araba. Sede Txagorritxu
    Asociación Española de PHP
  • gnanc*****@***kidetza.eus
Complete Info

Dr Deborah JG MACKAY

 SOUTHAMPTON. UNITED KINGDOM

  Investigator of research project - Contact person of registry

  • Research area/topic:
    Imprinting Disorders Finding Out Why (observational clinical study, mutation search - PLAGL1, ZFP57 and IGF2 genes) and genotype-phenotype correlation)
  • Faculty of Medicine, Faculty of Medicine - University of Southampton
  • dj**@***on.ac.uk
Complete Info

Pr Karen TEMPLE

 SOUTHAMPTON. UNITED KINGDOM

  Clinical expert - Investigator of research project - Manager of registry

  • Research area/topic:
    Imprinting Disorders Finding Out Why (observational clinical study, mutation search - PLAGL1, ZFP57 and IGF2 genes) and genotype-phenotype correlation)
  • Faculty of Medicine, Faculty of Medicine - University of Southampton
    University Hospital Southampton NHS Foundation Trust, Princess Anne Hospital
  • i**@***on.ac.uk
Complete Info

Other experts list that you may find interesting:

All the contact information provided is based on public data available in orpha.net.