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21 Result(s)

Partnership : Academics = Academics, Industrials = Industrials, Financial investitors = Financial investitors

    • 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
    • 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
    • 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
    • Hopital Necker - Enfants Malades
    • Département de génétique moléculaire
    • More details
    • FRANCE
    • ILE DE FRANCE
    • PARIS
    • Chromosomic errors and syndromic mental retardations
    • Hopital Necker - Enfants Malades
    • Département de génétique moléculaire
    • More details
    • FRANCE
    • LORRAINE
    • VANDOEUVRE-LES-NANCY
    • Genetics of Mental retardation: molecular characterization of chromosomal rearrangements (X and autosomes)
    • CHU de Nancy - Hôpital Brabois adultes
    • Laboratoire de génétique médicale
    • More details
    • GERMANY
    • Bayern
    • ERLANGEN
    • Functional characterisation of UBR1 gene in the pathogenesis of Johanson-Blizzard syndrome with special focus on pancreatic insufficiency (DFG)
    • Friedrich-Alexander-Universität Erlangen-Nürnberg
    • Humangenetisches Institut
    • More details
    • ITALY
    • LAZIO
    • ROMA
    • Study with high definition CGH Array on carriers patients of chromosomal rearrangements apparently balanced:phenotype-genotype correlation
    • Istituto CSS-Mendel
    • Laboratorio di Biologia Molecolare e Citogenetica
    • More details
    • ITALY
    • PIEMONTE
    • TORINO
    • Genetics basis of Mental Retardation
    • Azienda Sanitaria Ospedaliera O.I.R.M. - S. Anna - Università di Torino
    • Struttura Semplice di Genetica
    • More details
    • ITALY
    • PUGLIA
    • SAN GIOVANNI ROTONDO
    • Molecular genetics of cerebral cavernous malformations
    • IRCCS Ospedale Casa Sollievo della Sofferenza
    • Servizio di 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
    • 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
    • SPAIN
    • Castilla - León
    • VALLADOLID
    • Characterization of mental retardation of genetic origin
    • Universidad de Valladolid. Facultad de Medicina.
    • Laboratorio de Pediatría
    • More details
    • SPAIN
    • Comunidad Valenciana
    • VALENCIA
    • Application of CGH-array to detect genomic rearrangements responsible for idiophatic mental retardation
    • Hospital Universitario La Fe
    • Unidad de Genética y Diagnóstico Prenatal
    • More details
    • SPAIN
    • Comunidad Valenciana
    • VALENCIA
    • Industrials
    • High definition genomic screening of candidate genes for neurodevelopmental disorders
    • Hospital Universitario La Fe
    • Unidad de Genética y Diagnóstico Prenatal
    • More details
    • SPAIN
    • Extremadura
    • BADAJOZ
    • Study of patients with unexplained mental retardation, with positive family history and dismorphic features. Study with subtelomeric probes.
    • Hospital Materno Infantil de Badajoz
    • Unidad de Genética
    • More details
    • SPAIN
    • Madrid
    • MADRID
    • Detection of subtelomeric chromosomal anomalies in patients with idiopathic mental retardation by fluorescence in situ hybridization (FISH)
    • Hospital Universitario La Paz
    • Instituto de Genética Médica y Molecular
    • More details
    • SWITZERLAND
    • Suisse Romande
    • GENEVE
    • Function of the mental retardation genes PAK3 and ARGHEF6
    • Centre Médical Universitaire
    • Department of Neuroscience
    • More details
    • SWITZERLAND
    • Suisse Romande
    • GENEVE
    • Unbalanced chromosomal anomalies detection in patients with mental retardation and/or dysmorphism by CGH-Array (oligonucleotides chip - Agilent 244K): Geneva - Lausanne collaborative study
    • Centre Médical Universitaire
    • Laboratoire de Cytogénétique Clinique
    • More details
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Unbalanced chromosomal anomalies detection in patients with mental retardation and/or dysmorphism by CGH-Array (oligonucleotides chip - NimbleGen): Geneva - Lausanne collaborative study
    • Maternité, Centre Hospitalier Universitaire Vaudois (CHUV)
    • Laboratoire de Cytogénétique Constitutionnelle et Prénatale
    • More details
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Natural history in dysmorphic syndromes
    • Great Ormond Street Hospital for Children
    • NE Thames Regional Genetics Service
    • More details
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