25 Result(s)

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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
  • 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
• • FRANCE
  • MIDI-PYRENEES
  • TOULOUSE
  • Identification and validation of responsible genes for microphtalmia and anophtalmia in human
  • CHU de Toulouse - Hôpital Purpan
  • Service de génétique médicale (laboratoire)
  • More details
• • GREECE
  • ATTIKI
  • ATHENS
  • 
  • Evaluation of the clinical service provided in a Greek Department of Genetics, in the field of rare dysmorphic syndromes
  • Institute of Child Health
  • Department of Genetics
  • 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
  • LOMBARDIA
  • MILANO
  • Functional study of regulation dendritic spine by ampa receptors
  • Università degli Studi di Milano
  • Laboratorio di Farmacologia Molecolare
  • 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
  • Cataluña
  • BARCELONA
  • Characterisation and study of the implications of copy number variations in patients with X chromosome-related mental retardation
  • Hospital Clínic i Provincial de Barcelona
  • Laboratorio del Servicio de Bioquímica y Genética Molecular
  • 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
  • 
  • 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
• • UNITED KINGDOM
  • Oxfordshire
  • OXFORD
  • 
  • Genetic basis to developmental eye disorders
  • University of Oxford (Le Gros Clark Building)
  • Department of Physiology, Anatomy and Genetics
  • More details