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    • FRANCE
    • CENTRE
    • TOURS
    • Search for mutations in NLGN4X and NLGN3 genes in case of intellectual deficiencies with autism
    • CHRU de Tours - H˘pital Bretonneau
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of Asperger syndrome X- linked, type 1 and 2 (NLGN3 and NLGN4X gene: sequencing of the entire coding region)
    • CGC Genetics / Centro de GenÚtica ClÝnica
    • More information
    • FRANCE
    • LANGUEDOC-ROUSSILLON
    • N╬MES
    • Search for mutations in NLGN3, NLGN4X, RAB39B genes in case of autism and X-linked mental retardation
    • CHU de Nţmes - H˘pital Caremeau
    • More information