Agentes involucrados
: Académicos/-as
= 
, Industriales
= 
, Inversores económicos
= 
-
- ALEMANIA
- 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
- Para más detalles
-
- ALEMANIA
- Baden-Württemberg
- TÜBINGEN
- Phenotype-genotype correlation in hereditary degeneration of the retina and the optic nerve (extended function analysis and differentiation, neuro-ophthalmology, mouse models)
- Universität Tübingen
- Forschungsinstitut für Augenheilkunde
- Para más detalles
-
- ALEMANIA
- Baden-Württemberg
- TÜBINGEN
- HOPE2: Hereditary Retinal Disorders - From Patients Towards Therapies to each project: Translation of novel diagnostics procedures and evaluation of experimental therapies in hereditary retinal disorders (subproject 2)
- Universität Tübingen
- Forschungsinstitut für Augenheilkunde
- Para más detalles
-
- ALEMANIA
- 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
- Para más detalles
-
- NGFN plus : IG German Mental Retardation Network (coordination)
- Universitätsklinikum Erlangen
- Humangenetisches Institut
- Para más detalles
-
- 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
- Para más detalles
-
- 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
- Para más detalles
-
- 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
- Para más detalles
-
- ALEMANIA
- Bayern
- REGENSBURG
- HOPE2: Hereditary Retinal Disorders - From Patients Towards Therapies: Integrated diagnostics in hereditary retinal disorders (subproject 3)
- Universitätsklinikum Regensburg
- Zentrum und Institut für Humangenetik Regensburg
- Para más detalles
-
- 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
- Para más detalles
-
- 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
- Para más detalles
-
- Genotype phenotype correlation of hereditary eye diseases
- Universitätsklinikum Gießen und Marburg GmbH, Standort Gießen
- Klinik und Poliklinik für Augenheilkunde
- Para más detalles
-
- Diagnosis and therapy of hereditary retinal diseases
- Universitätsklinikum Gießen und Marburg GmbH, Standort Gießen
- Klinik und Poliklinik für Augenheilkunde
- Para más detalles
-
- ALEMANIA
- 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
- Para más detalles
-
- ALEMANIA
- 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
- Para más detalles
-
- ALEMANIA
- 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
- Para más detalles
-
- ALEMANIA
- Saarland
- HOMBURG
- Visual impairment and blindness in multiple-handicapped children
- Universitätsklinikum des Saarlandes
- AG Kinder- & Neuroophthalmologie
- Para más detalles
-
- 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
- Para más detalles
-
- 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
- Para más detalles
-
- CANADA
- Colombie-Britannique
- VANCOUVER
- FORGE - Finding of Rare Disease Genes in Canada
- University of British Columbia
- Faculty of Medicine
- Para más detalles
-
- CANADA
- Ontario
- OTTAWA, ONTARIO
- FORGE - Finding of Rare Disease Genes in Canada
- University of Ottawa
- Faculty of Medicine -
- Para más detalles
-
- FORGE - Finding of Rare Disease Genes in Canada
- Centre hospitalier universitaire Sainte-Justine
- Pédiatrie
- Para más detalles
-
- ESPAÑA
- Comunidad Valenciana
- VALENCIA
- Rastreo genómico de alta resolución en genes candidatos de trastornos del neurodesarrollo
- Hospital Universitario La Fe (Campanar)
- Unidad de Genética y Diagnóstico Prenatal
- Para más detalles
-
- The prevalence and genetic background of hereditary hearing impairment in Estonia
- Children's Clinic of Tartu University
- Department of Paediatrics
- Para más detalles
-
- 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
- Para más detalles
-
- 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
- Para más detalles
-
- FRANCIA
- ILE-DE-FRANCE
- PARIS
- Identification of the molecular basis for unexplained mental retardation
- CHU Paris - Hôpital Necker - Enfants Malades
- Département de génétique
- Para más detalles
-
- FRANCIA
- ILE-DE-FRANCE
- PARIS
- Chromosomic errors and syndromic mental retardations
- CHU Paris - Hôpital Necker - Enfants Malades
- Département de génétique
- Para más detalles
-
- FRANCIA
- ILE-DE-FRANCE
- PARIS
- Characterization of new genes involved in non-syndromic and syndromic deafness (especially Usher syndrome) and corresponding impairement physiopathology
- Institut Pasteur
- Unité de Génétique et physiologie cellulaire
- Para más detalles
-
- ITALIA
- LOMBARDIA
- CUSANO MILANINO
- Molecular analysis of families cosegregating X-linked mental retardation
- Istituto Auxologico Italiano
- Laboratorio di Biologia Molecolare
- Para más detalles
-
- Identification of the function of genes muteted in X-linked mental retardation
- Università degli Studi di Milano
- Laboratorio di Farmacologia Molecolare
- Para más detalles
-
- Genetics basis of Mental Retardation
- A.O. Città della Salute e della Scienza di Torino - Ospedale Regina Margherita
- Struttura Semplice di Genetica
- Para más detalles
-
- 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
- Para más detalles
-
- 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
- Para más detalles
-
- Neuro-vascular interactions in the developing retina: exploring the cellular ethiology of Norrie Disease and testing the rationale for experimental therapeutic approaches in animal models
- Consiglio Nazionale delle Ricerche CNR
- Area della Ricerca
- Para más detalles
-
- Pathogenetic mechanisms and therapeutic perspectives for connexin related hereditary hearing loss
- Venetian Institute of Molecular Medicine
- Centro Interdipartimentale per lo Studio dei Segnali Cellulari
- Para más detalles
-
- 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
- Para más detalles
-
- SUIZA
- Suisse Alémanique
- SCHWERZENBACH
- Molecular mechanisms of pathogenesis and clinical variability in Norrie disease, a familial syndrome of blindness, deafness and mental retadation and allelic disorders (Coats disease, exsudative vitroretinopathy)
- Universität Zürich
- Institüt für Medizinische Molekulargenetik - Institute of Medical Molecular Genetics
- Para más detalles
-
- SUIZA
- 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
- Para más detalles
