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8 Result(s)

Result(s)sorted by
Speciality(ies)/objective(s)
(7)
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(2)
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Purpose(s)
(7)
(1)
(1)
Quality management
(4)
(6)
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Result(s)sorted by

Caption : Accreditation =Accreditation
;

    • Accreditation
    • Molecular diagnosis of idiopathic ventricular fibrillation, not Brugada type (SCN5A gene)
    • CHU de Nantes - Institut de Biologie
    • Purpose(s) : Post-natal diagnosis, Pre-symptomatic diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Targeted mutation analysis, Mutation scanning/screening and sequence analysis of selected exons, Sequence analysis: entire coding region
    • Technical procedure(s) : NGS sequencing (except WES), Sanger sequencing
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • NANTES
    • Accreditation
    • Molecular diagnosis of Cardiac Rhythm Disease (multigene panel; 43 genes)
    • AMC - Academisch Medisch Centrum
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : NGS sequencing (except WES)
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of Conduction Abnormalities (multigene panel; 33 genes)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : NGS sequencing (except WES)
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of paroxysmal familial ventricular fibrillation type 1 and 2 (DPP6, SCN5A genes)
    • Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
    • Purpose(s) : Somatic genetics
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • DORTMUND
    • Molecular diagnosis of idiopathic ventricular fibrillation, not Brugada type (SCN5A, DPP6 genes)
    • Sistemas Genómicos S.L.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of Familial paroxysmal ventricular fibrillation, not Brugada type (SCN5A 3p22.2 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
    • Postnatal molecular diagnosis of idiopathic ventricular fibrillation, not Brugada type (sequence analysis of the entire coding region of SCN5A gene)
    • Azienda Ospedaliera di Padova
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • Technical procedure(s) : NGS sequencing (except WES), Sanger sequencing
    • More information
    • ITALY
    • VENETO
    • PADOVA
    • Postnatal molecular diagnosis of idiopathic ventricular fibrillation (SCN5A gene:deletion/duplication analysis by MLPA; mutation screening and sequencing of the entire coding region)
    • National institute of legal medicine
    • 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, Deletion / Duplication analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • ROMANIA
    • BUCURESTI
    • BUCURESTI