There is no disease so rare
that it does not deserve attention

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• • CANADA
  • Colombie-Britannique
  • VANCOUVER
  • FORGE - Finding of Rare Disease Genes in Canada
  • University of British Columbia
  • Faculty of Medicine
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• • CANADA
  • Ontario
  • OTTAWA, ONTARIO
  • FORGE - Finding of Rare Disease Genes in Canada
  • University of Ottawa
  • Faculty of Medicine -
  • More details
• • CANADA
  • Québec
  • MONTREAL
  • FORGE - Finding of Rare Disease Genes in Canada
  • Centre hospitalier universitaire Sainte-Justine
  • Pédiatrie
  • More details
• • FRANCE
  • MIDI-PYRENEES
  • TOULOUSE
  • Analysis of genes involved in ocular development anomalies
  • CHU de Toulouse - Hôpital Purpan
  • Service de génétique médicale (Biologie)
  • More details
• • GERMANY
  • Berlin
  • BERLIN
  • Genetic disturbance of sex development / Disorders of sex development (BMBF Network Intersexuality)
  • Charité - Universitätsmedizin Berlin (CVK)
  • Institut für Experimentelle Pädiatrische Endokrinologie
  • More details
• • GERMANY
  • Hamburg
  • HAMBURG
  • Genotype-phenotype correlation of patients with WT1 gene mutation
  • Universitätsklinikum Hamburg-Eppendorf
  • Gesellschaft für Pädiatrische Nephrologie
  • More details
• • GERMANY
  • Hamburg
  • HAMBURG
  • Genotype-phenotype correlation of patients with WT1 gene mutation
  • Universitätsklinikum Hamburg-Eppendorf
  • Klinik und Poliklinik für Kinder- und Jugendmedizin
  • More details
• • GERMANY
  • Hessen
  • GIEßEN
  • Genotype phenotype correlation of hereditary eye diseases
  • Universitätsklinikum Gießen und Marburg GmbH, Standort Gießen
  • Klinik und Poliklinik für Augenheilkunde
  • More details
• • GERMANY
  • Saarland
  • HOMBURG
  • Visual impairment and blindness in multiple-handicapped children
  • Universitätsklinikum des Saarlandes
  • AG Kinder- & Neuroophthalmologie
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• • GERMANY
  • Sachsen
  • WEIßWASSER
  • WT1 gene: Direct sequencing of the coding regions
  • Praxis Dr. Mato Nagel
  • Molekulargenetisches Labor
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• • ITALY
  • FRIULI VENEZIA GIULIA
  • UDINE
  • PAX6 mutations in aniridia patients
  • Azienda Ospedaliero-Universitaria "Santa Maria della Misericordia" di Udine
  • Laboratorio di Genetica Molecolare
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• • UNITED KINGDOM
  • Oxfordshire
  • OXFORD
  • 
  • Genetic basis to developmental eye disorders
  • Le Gros Clark Building - University of Oxford
  • Neuroscience
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• • UNITED KINGDOM
  • Wiltshire
  • SALISBURY
  • FISH studies in 194 patients with Aniridia and/or WAGR syndrome
  • Salisbury District Hospital
  • Wessex Regional Genetics Laboratory - Molecular Cytogenetics
  • More details