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    • Collection and characterisation of cases with a small supernumerary marker chomosome with the goal of a genotype phenotype correlation
    • Universitätsklinikum Jena
    • Molekulare Zytogenetik (FISH Labor)
    • More details
    • GERMANY
    • Thüringen
    • JENA
    • Diagnostic potential and reliability of array-CGH technique in chorionic villi samplings. Detection of cryptic chromosome abnormalities and possible fetoplacental discrepancies
    • Hospital Clínic de Barcelona
    • Laboratorio de Citogenética y Genética Clínica
    • More details
    • SPAIN
    • Cataluña
    • BARCELONA
    • Chromosomal anomaly
    • Karolinska University Hospital - Solna
    • Department of clinical genetics
    • More details
    • SWEDEN
    • Stockholms läns landsting
    • STOCKHOLM
    • NIHR BioResource - Rare Disease: SPEED - Specialist Pathology: Evaluating Exomes in Diagnostics
    • Wellcome Trust/MRC Building
    • Cambridge Institute for Medical Research
    • More details
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • The Deciphering Developmental Disorders (the DDD study)
    • Wellcome Trust Sanger Institute
    • DECIPHER
    • More details
    • UNITED KINGDOM
    • Cambridgeshire
    • HINXTON
    • Exploring the Genetics of Renal Developmental Disease
    • Royal Devon and Exeter Hospital - Wonford site
    • Department of Urology
    • More details
    • UNITED KINGDOM
    • Devon
    • EXETER
    • 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
    • UNITED KINGDOM
    • West Midlands
    • BIRMINGHAM