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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
    • More details
    • GERMANY
    • Saarland
    • HOMBURG
    • Genotype phenotype correlation and genetic characterization of mutations leading to albinism
    • Universitätsklinikum des Saarlandes
    • AG Kinder- & Neuroophthalmologie
    • More details
    • 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
    • More details
    • ITALY
    • LOMBARDIA
    • MILANO
    • Academics
    • 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
    • More details
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • NIHR BioResource - Rare Disease: SPEED - Specialist Pathology: Evaluating Exomes in Diagnostics
    • Wellcome Trust/MRC Building
    • Cambridge Institute for Medical Research
    • More details
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM
    • NIPSIGEN - Clinical translation of non-invasive prenatal diagnosis (NIPD) for single gene disorders (Health Innovation Challenge Fund)
    • Birmingham Women's NHS Foundation Trust
    • Regional Genetics Unit
    • More details