As doenças raras são raras, mas os doentes
com doenças raras são muito numerosos

Parceria : Académicos = , Industriais = , Investidores financeiros =

• • ALEMANHA
  • 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
  • Mais detalhes
• • ALEMANHA
  • 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
  • Mais detalhes
• • ALEMANHA
  • Bayern
  • ERLANGEN
  • NGFN plus : IG German Mental Retardation Network (coordination)
  • Friedrich-Alexander-Universität Erlangen-Nürnberg
  • Humangenetisches Institut
  • Mais detalhes
• • ALEMANHA
  • 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
  • Friedrich-Alexander-Universität Erlangen-Nürnberg
  • Humangenetisches Institut
  • Mais detalhes
• • ALEMANHA
  • 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
  • Mais detalhes
• • ALEMANHA
  • 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
  • Mais detalhes
• • ALEMANHA
  • 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
  • Mais detalhes
• • ALEMANHA
  • 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
  • Universität Bonn
  • Institut für Humangenetik
  • Mais detalhes
• • ALEMANHA
  • 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
  • Mais detalhes
• • ALEMANHA
  • 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
  • Mais detalhes
• • ALEMANHA
  • Sachsen
  • DRESDEN
  • NGFN plus : IG German Mental Retardation Network - MR Centre Dresden (Project 7): Clinical characterization, molecular karyotyping and gentype phenotype correlations
  • Medizinische Fakultät Carl Gustav Carus der TU Dresden
  • Institut für Klinische Genetik
  • Mais detalhes
• • BELGICA
  • 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
  • Mais detalhes
• • CANADA
  • Colombie-Britannique
  • VANCOUVER
  • FORGE - Finding of Rare Disease Genes in Canada
  • University of British Columbia
  • Faculty of Medicine
  • Mais detalhes
• • CANADA
  • Ontario
  • OTTAWA, ONTARIO
  • FORGE - Finding of Rare Disease Genes in Canada
  • University of Ottawa
  • Faculty of Medicine -
  • Mais detalhes
• • CANADA
  • Québec
  • MONTREAL
  • FORGE - Finding of Rare Disease Genes in Canada
  • Centre hospitalier universitaire Sainte-Justine
  • Pédiatrie
  • Mais detalhes
• • ESPANHA
  • Comunidad Valenciana
  • VALENCIA
  • 
  • High definition genomic screening of candidate genes for neurodevelopmental disorders
  • Hospital Universitario La Fe (Campanar)
  • Unidad de Genética y Diagnóstico Prenatal
  • Mais detalhes
• • ESPANHA
  • País Vasco
  • BARAKALDO
  • Genetic approach to Rett syndrome and its variants. Clinical and molecular characterization of neuropsychiatric phenotypes that overlap
  • Hospital Universitario Cruces - Osakidetza
  • Laboratorio de Genética Molecular
  • Mais detalhes
• • 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
  • Mais detalhes
• • FRANCA
  • 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
  • Mais detalhes
• • FRANCA
  • ILE-DE-FRANCE
  • PARIS
  • Identification of the molecular basis for unexplained mental retardation
  • CHU Paris - Hôpital Necker - Enfants Malades
  • Département de génétique
  • Mais detalhes
• • FRANCA
  • ILE-DE-FRANCE
  • PARIS
  • Chromosomic errors and syndromic mental retardations
  • CHU Paris - Hôpital Necker - Enfants Malades
  • Département de génétique
  • Mais detalhes
• • ITALIA
  • LAZIO
  • ROMA
  • Study of criptic anomalies of mental retardation
  • Policlinico Universitario "A. Gemelli"
  • Servizio di Genetica Medica
  • Mais detalhes
• • ITALIA
  • PIEMONTE
  • TORINO
  • Genetics basis of Mental Retardation
  • A.O. Città della Salute e della Scienza di Torino - Ospedale Regina Margherita
  • Struttura Semplice di Genetica
  • Mais detalhes
• • ITALIA
  • 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
  • Mais detalhes
• • ITALIA
  • 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
  • Mais detalhes
• • SUICA
  • 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
  • Mais detalhes