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  3. INTELLECTUAL DISABILITY-SPARSE HAIR-BRACHYDACTYLY SYNDROME Experts by country

INTELLECTUAL DISABILITY-SPARSE HAIR-BRACHYDACTYLY SYNDROME Experts

We have collected the completed list of expert related to INTELLECTUAL DISABILITY-SPARSE HAIR-BRACHYDACTYLY SYNDROME using public data available on different databases.

INTELLECTUAL DISABILITY-SPARSE HAIR-BRACHYDACTYLY SYNDROME Experts map



If you find this map or researchers for INTELLECTUAL DISABILITY-SPARSE HAIR-BRACHYDACTYLY SYNDROME useful, maybe you will be also interested in other rare diseases proffesionals like our fragile x syndrome expert list ,or our beta-thalassemia expert list

INTELLECTUAL DISABILITY-SPARSE HAIR-BRACHYDACTYLY SYNDROME Experts list

Pr Dagmar WIECZOREK

 DÜSSELDORF. GERMANY

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

  • Research area/topic:
    CHROMATIN-Net: Intellectual disability (ID) and syndromic entities associated with mutations in the SWI/SNF complex
  • Universitätsklinikum Düsseldorf
    Heinrich-Heine-Universität Düsseldorf
  • dagmar.w********@***_duesseldorf.de
Complete Info

Pr André REIS

 ERLANGEN. GERMANY

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

  • Research area/topic:
    CHROMATIN-Net: Network on cognitive impairment disorders with defective chromatin (coordination)
  • Humangenetisches Institut am Universitätsklinikum Erlangen
  • Andre*****@***erlangen.de
Complete Info

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:
    CHROMATIN-Net: The nucleosome landscape of Coffin-Siris and Nicolaides-Baraitser syndrome patients with mutations in the SWI/SNF complex
  • Universitätsklinikum Essen
    Universitätsklinikum Essen
Complete Info

Dr Tim M. STROM

 MÜNCHEN. GERMANY

  Responsible for diagnostic tests - Investigator of research project

  • Research area/topic:
    CHROMATIN-Net: Whole Genome Sequencing and Analysis
  • Helmholtz Zentrum München
  • TimS****@***mholtz_muenchen.de
Complete Info

Pr R.C. [Raoul] HENNEKAM

 AMSTERDAM. NETHERLANDS

  Clinical expert - Investigator of research project - Researcher

  • Research area/topic:
    Causes of Nicolaides-Baraitser Syndrome
  • Clinical Genetics Department, Level 4, York House, University College London Hospitals, NHS Foundation Trust
    Emma Kinderziekenhuis, Amsterdam UMC, locatie AMC
    UMCG - Universitair Medisch Centrum Groningen
  • r.c.he******@***.uva.nl
Complete Info

Pr R.C. [Raoul] HENNEKAM

 GRONINGEN. NETHERLANDS

  Clinical expert - Investigator of research project - Researcher

  • Research area/topic:
    Causes of Nicolaides-Baraitser Syndrome
  • Clinical Genetics Department, Level 4, York House, University College London Hospitals, NHS Foundation Trust
    Emma Kinderziekenhuis, Amsterdam UMC, locatie AMC
    UMCG - Universitair Medisch Centrum Groningen
  • r.c.he******@***.uva.nl
Complete Info

Pr R.C. [Raoul] HENNEKAM

 LONDON. UNITED KINGDOM

  Clinical expert - Investigator of research project - Researcher

  • Research area/topic:
    Causes of Nicolaides-Baraitser Syndrome
  • Clinical Genetics Department, Level 4, York House, University College London Hospitals, NHS Foundation Trust
    Emma Kinderziekenhuis, Amsterdam UMC, locatie AMC
    UMCG - Universitair Medisch Centrum Groningen
  • r.c.he******@***.uva.nl
Complete Info

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