Rare diseases are rare, but
rare disease patients are numerous

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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
  • AQUITAINE
  • BORDEAUX
  • Molecular analysis of patients affected by oculo-cutaneous albinism
  • CHU de Bordeaux-GH Pellegrin
  • Laboratoire Maladies Rares : Génétique et Métabolisme
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• • GERMANY
  • Hessen
  • GIEßEN
  • Genotype phenotype correlation of hereditary eye diseases
  • Universitätsklinikum Gießen und Marburg GmbH, Standort Gießen
  • Klinik und Poliklinik für Augenheilkunde
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• • GERMANY
  • Saarland
  • HOMBURG
  • Genotype phenotype correlation and genetic characterization of mutations leading to albinism
  • Universitätsklinikum des Saarlandes
  • AG Kinder- & Neuroophthalmologie
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• • GERMANY
  • Saarland
  • HOMBURG
  • Topographics of the visual cortex in albinism and in conductors of oculo-cutaneous albinism type OCA1A
  • Universitätsklinikum des Saarlandes
  • AG Kinder- & Neuroophthalmologie
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• • GERMANY
  • Schleswig-Holstein
  • LÜBECK
  • Genotype phenotype correlation and genetic characterization of mutations leading to albinism
  • Universitätsklinikum Schleswig-Holstein - Campus Lübeck
  • Institut für Humangenetik
  • More details
• • ITALY
  • LAZIO
  • ROMA
  • GENESKIN: European network on rare genetic skin diseases (coordination)
  • Istituto Dermopatico dell'Immacolata - IRCCS
  • Laboratorio di Biologia Molecolare e Cellulare
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• • ITALY
  • LOMBARDIA
  • MILANO
  • 
  • Differential diagnosis of ocular and oculocutaneous albinism in the italian population: diagnostic workup and multidisciplinary study using molecular genetic characterization of the associated genes.
  • Ospedale Niguarda Ca' Granda
  • S.S. Genetica Medica - S.C. Analisi Chimico Cliniche e Patologia Clinica
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• • SPAIN
  • Madrid
  • MADRID
  • Genetic diagnosis and possible treatments for albinism
  • Centro Nacional de Biotecnología (CNB-CSIC)
  • Grupo de Modelos animales para manipulación genética - Dep. de Biología Molecular y Celular
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• • SPAIN
  • Madrid
  • MADRID
  • 
  • Animal and cellular models for the study of neurosensorial deafness and hearing disorders associated to exposure to excesive noise
  • Instituto de Investigaciones Biomédicas "Alberto Sols" (CSIC-UAM)
  • Grupo/Laboratorio de Neurobiología de la Audición / Servicio de Evaluación Neurofuncional no Invasiva
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