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7 Result(s)

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Speciality(ies)/objective(s)
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(3)
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(1)
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(7)
(4)
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(5)
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Result(s)sorted by

Caption : Accreditation =Accreditation
;

    • Accreditation
    • Molecular diagnosis of predisposition to Asperger syndrome (NLGN3, NLGN4X genes)
    • Praxis für Humangenetik Freiburg
    • Purpose(s) : Post-natal diagnosis, Risk assessment
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of the susceptibility to Asperger syndrome (NLGN3, NLGN4X genes)
    • Reference Laboratory Genetics
    • Purpose(s) : Post-natal diagnosis, Risk assessment
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Cataluña
    • L'HOSPITALET DE LLOBREGAT
    • Accreditation
    • Molecular diagnosis of predisposition to Asperger syndrome ((NLGN3, NLGN4X genes: sequencing)
    • CeGaT GmbH
    • Purpose(s) : Post-natal diagnosis, Risk assessment
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Search for mutation in NLGN4X and NLGN3 genes in case of intellectual disability with autism
    • CHRU de Tours - Hôpital Bretonneau
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region
    • Technical procedure(s) : Sanger sequencing, PCR based techniques
    • More information
    • FRANCE
    • CENTRE
    • TOURS
    • 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 Genética Clínica
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Molecular diagnosis of susceptibility to Asperger syndrome (NLGN3 gene)
    • IMEGEN - Instituto de Medicina Genómica
    • Purpose(s) : Post-natal diagnosis, Risk assessment
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Diagnosis of Asperger syndrome (NLGN3 candidate gene)
    • Bioarray
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : NGS sequencing (except WES)
    • More information
    • SPAIN
    • Comunidad Valenciana
    • ELCHE