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Ricerca per malattia/gene

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24 Risultato/i

Partnership : Accademici = Accademici , Industria = Industria , Investitori finanziari = Investitori finanziari

    • BELGIO
    • 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
    • Ulteriori dettagli
    • CANADA
    • Colombie-Britannique
    • VANCOUVER
    • FORGE - Finding of Rare Disease Genes in Canada
    • University of British Columbia
    • Faculty of Medicine
    • Ulteriori dettagli
    • CANADA
    • Ontario
    • OTTAWA, ONTARIO
    • FORGE - Finding of Rare Disease Genes in Canada
    • University of Ottawa
    • Faculty of Medicine -
    • Ulteriori dettagli
    • CANADA
    • Québec
    • MONTREAL
    • FORGE - Finding of Rare Disease Genes in Canada
    • Centre hospitalier universitaire Sainte-Justine
    • Pédiatrie
    • Ulteriori dettagli
    • 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
    • Ulteriori dettagli
    • FRANCIA
    • 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
    • Ulteriori dettagli
    • FRANCIA
    • ILE-DE-FRANCE
    • PARIS
    • Identification of the molecular basis for unexplained mental retardation
    • CHU Paris - Hôpital Necker - Enfants Malades
    • Laboratoire de Génétique
    • Ulteriori dettagli
    • FRANCIA
    • ILE-DE-FRANCE
    • PARIS
    • Chromosomic errors and syndromic mental retardations
    • CHU Paris - Hôpital Necker - Enfants Malades
    • Laboratoire de Génétique
    • Ulteriori dettagli
    • GERMANIA
    • Baden-Württemberg
    • HEIDELBERG
    • NGFN plus : IG German Mental Retardation Network - MR Centre Heidelberg (Project 9): Mutation screenings and functional characterisation on candidate genes
    • Universitätsklinikum Heidelberg
    • Abteilung Molekulare Humangenetik
    • Ulteriori dettagli
    • GERMANIA
    • Baden-Württemberg
    • TÜBINGEN
    • NGFN plus : IG German Mental Retardation Network - MR Zentrum Tübingen (project 3): High resolution SNP microarrays for identification of genome imbalances and segmental UPD's. Molecular (MLPA, qPCR) and molecular cytogenetic (FISH) techniques for validation of Copy Number Variants.
    • Universitätsklinikum Tübingen
    • Medizinische Genetik Tübingen
    • Ulteriori dettagli
    • GERMANIA
    • Bayern
    • ERLANGEN
    • NGFN plus : IG German Mental Retardation Network (coordination)
    • Universitätsklinikum Erlangen
    • Humangenetisches Institut
    • Ulteriori dettagli
    • GERMANIA
    • Bayern
    • ERLANGEN
    • NGFN plus : IG German Mental Retardation Network - MR Centre Erlangen (Project 1): Identification, validation and functional characterization of disease causing genes and proteines in patients with mental retardation of unkown cause
    • Universitätsklinikum Erlangen
    • Humangenetisches Institut
    • Ulteriori dettagli
    • GERMANIA
    • Bayern
    • MÜNCHEN
    • BNE: BrainNet Europe II: European brain tissue bank - Network for clinical neuroscience and basic research (coordination)
    • Ludwig-Maximilians-Universität München
    • Zentrum für Neuropathologie und Prionforschung
    • Ulteriori dettagli
    • GERMANIA
    • Bayern
    • MÜNCHEN
    • NGFN plus : IG German Mental Retardation Network - MR Centre Munich (project4): Genome-wide hybridization of genomic DNA with oligonucleotide-based arrays
    • Technische Universität München
    • Institut für Humangenetik
    • Ulteriori dettagli
    • GERMANIA
    • Berlin
    • BERLIN
    • NGFN plus : IG German Mental Retardation Network -MR Centre Berlin (Teilprojekt 2): Array CGH for detection of submicroscopic genome imbalances, homozygosity mapping using SNP arrays
    • Max-Planck-Institut für molekulare Genetik
    • Abteilung Human Molecular Genetics
    • Ulteriori dettagli
    • GERMANIA
    • Nordrhein-Westfalen
    • BONN
    • NGFN plus : IG German Mental Retardation Network - MR Centre Bonn (Project 5): identification of candidate genes for mental retardation by the detection and analysis of submicroscopic CNCs
    • Universitätsklinikum Bonn
    • Institut für Humangenetik
    • Ulteriori dettagli
    • GERMANIA
    • Nordrhein-Westfalen
    • ESSEN
    • NGFN plus : IG German Mental Retardation Network - MR Centre Essen (Project 8): genotype phenotype correlations in patients with mental retardation
    • Universitätsklinikum Essen
    • Institut für Humangenetik
    • Ulteriori dettagli
    • GERMANIA
    • Nordrhein-Westfalen
    • MÜNSTER
    • NGFN plus : IG German Mental Retardation Network - MR Centre Münster (Project 6): Identification of diseases causing genes in mental retardation
    • Universitätsklinikum Münster
    • Institut für Humangenetik
    • Ulteriori dettagli
    • GERMANIA
    • Sachsen
    • DRESDEN
    • NGFN plus : IG German Mental Retardation Network - MR Centre Dresden (Project 7): Clinical characterization, molecular karyotyping and gentype phenotype correlations
    • Universitätsklinikum Carl Gustav Carus an der TU Dresden
    • Institut für Klinische Genetik
    • Ulteriori dettagli
    • ITALIA
    • PIEMONTE
    • TORINO
    • Ricerca clinica sulle principali Sindromi associate a craniosinostosi
    • A.O. Città della Salute e della Scienza di Torino - Ospedale Regina Margherita
    • Struttura Semplice di Genetica
    • Ulteriori dettagli
    • ITALIA
    • SICILIA
    • TROINA
    • Utilità dell'array-CGH 244K nel riconoscimento di riarrangiamenti cromosomici criptici nel ritardo mentale e nell'autismo
    • IRCCS OASI Maria Santissima
    • U.O.C.di Pediatria e Genetica Medica
    • Ulteriori dettagli
    • ITALIA
    • SICILIA
    • TROINA
    • Utilità dell'array-CGH 244K nel riconoscimento di riarrangiamenti cromosomici criptici nel ritardo mentale e nell'autismo
    • IRCCS OASI Maria Santissima
    • Laboratorio di Diagnosi Genetica
    • Ulteriori dettagli
    • SPAGNA
    • Comunidad Valenciana
    • VALENCIA
    • Industria
    • High definition genomic screening of candidate genes for neurodevelopmental disorders
    • Hospital Universitario La Fe (Campanar)
    • Unidad de Genética y Diagnóstico Prenatal
    • Ulteriori dettagli
    • SVIZZERA
    • Suisse Alémanique
    • SCHWERZENBACH
    • NGFN plus : IG German Mental Retardation Network - MR Centre Erlangen (Project 1): Identification, validation and functional characterization of disease causing genes and proteines in patients with mental retardation of unkown cause
    • Universität Zürich
    • IMG - Institut für Medizinische Genetik
    • Ulteriori dettagli