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    • BELGIUM
    • OOST-VLAANDEREN
    • GENT
    • Molecular genetic investigation of apparently balanced translocations in patients with mental retardation and multiple congenital malformations.
    • Ghent University Hospital - UZGent
    • Center for Medical Genetics Ghent
    • More details
    • CANADA
    • Ontario
    • OTTAWA
    • AcademicsIndustrials
    • Emerging team in rare diseases: achieving the "triple aim" for inborn errors of metabolism
    • Children's Hospital of Eastern Ontario
    • Newborn Screening Ontario
    • More details
    • CANADA
    • Ontario
    • OTTAWA, ONTARIO
    • AcademicsIndustrials
    • Emerging team in rare diseases: achieving the "triple aim" for inborn errors of metabolism
    • University of Ottawa
    • Department of Epidemiology and Community Medicine
    • More details
    • CANADA
    • Québec
    • SHERBROOKE
    • New roles for copper metabolism proteins in meiotic differentiation
    • Centre de développement des biotechnologies (CDB) de Sherbrooke
    • Département de Biochimie
    • More details
    • ESTONIA
    • Tartu
    • TARTU
    • Development of novel DNA diagnostic technologies for the detection of structural chromosomal abnormalities in case of mental retardation (EFT 5467).
    • University of Tartu
    • The Institute of Molecular and Cell Biology
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • BONDY
    • Cryptic anomalies by CGH array in children with mental retardation and ophtalmologic anomalies
    • CHU Paris Seine-Saint-Denis - Hôpital Jean Verdier
    • Laboratoire de cytogénétique et biologie de la reproduction
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Identification of the molecular basis for unexplained mental retardation
    • CHU Paris - Hôpital Necker-Enfants Malades
    • Laboratoire de Génétique Moléculaire
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Chromosomic errors and syndromic mental retardations
    • CHU Paris - Hôpital Necker-Enfants Malades
    • Laboratoire de Génétique Moléculaire
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Evaluation of diagnosis and treatment protocols and long-term follow-up of errors of metabolism
    • CHU Paris - Hôpital Necker-Enfants Malades
    • Unité fonctionnelle métabolisme
    • More details
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Evaluation of diagnosis and treatment protocols and long-term follow-up of errors of metabolism
    • CHU Paris - Hôpital Robert Debré
    • Service de neurologie pédiatrique et des maladies métaboliques
    • More details
    • GERMANY
    • Berlin
    • BERLIN
    • Search and functional characterisation of genes in X-linked and autosomal recessive forms of mental retardation
    • Max-Planck-Institut für molekulare Genetik
    • Abteilung Human Molecular Genetics
    • More details
    • IRELAND
    • County Dublin
    • DUBLIN
    • A prospective study on the numbers of Irish Travellers attending the metabolic clinic in Dublin
    • Our Lady's Children's Hospital
    • National Centre for Medical Genetics
    • More details
    • ITALY
    • LOMBARDIA
    • CUSANO MILANINO
    • Molecular analysis of families cosegregating X-linked mental retardation
    • Istituto Auxologico Italiano
    • Laboratorio di Biologia Molecolare
    • More details
    • ITALY
    • LOMBARDIA
    • MILANO
    • Identification of the function of genes muteted in X-linked mental retardation
    • Università degli Studi di Milano - Scienze Farmacologiche e Biomolecolari
    • Laboratorio di Farmacologia Molecolare
    • More details
    • ITALY
    • PIEMONTE
    • TORINO
    • Genetics basis of Mental Retardation
    • A.O. Città della Salute e della Scienza di Torino - Ospedale Regina Margherita
    • Struttura Semplice di Genetica
    • More details
    • ITALY
    • SICILIA
    • TROINA
    • Usefulness of 244K array-cgh in the ascertainment of cryptic chromosomal rearrangements in Mental Retardation and Autism
    • IRCCS OASI Maria Santissima
    • U.O.C.di Pediatria e Genetica Medica
    • More details
    • ITALY
    • SICILIA
    • TROINA
    • Usefulness of 244K array-cgh in the ascertainment of cryptic chromosomal rearrangements in Mental Retardation and Autism
    • IRCCS OASI Maria Santissima
    • Laboratorio di Diagnosi Genetica
    • More details
    • POLAND
    • Warszawa
    • WARSAW
    • Research on intellectual deficit ethiopathogenesis. Mapping and identification of genes localized on chromosome X using CGH microarrays.
    • Institute of mother and child / Instytut Matki i Dziecka
    • Department of medical genetics - Zespol Pracowni Genetyki Molekularnej
    • 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
    • Lothian
    • EDINBURGH
    • Genetic disorders of human brain development
    • Western General Hospital
    • MRC Human Genetics Unit
    • 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