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12 Result(s)

Result(s)sorted by
Speciality(ies)/objective(s)
(12)
(2)
Purpose(s)
(12)
Quality management
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(6)
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Result(s)sorted by

Caption : Accreditation =Accreditation
;

    • Molecular diagnosis of secondary polycythemia (EGLN1 gene)
    • CHU Paris IdF Ouest - HEGP Hôpital Européen Georges Pompidou
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Accreditation
    • Molecular diagnosis of familial erythrocytosis 1-4 (EGLN1, EPAS1, EPOR, VHL genes)
    • Medizinisches Versorgungszentrum (MVZ) Dr. Eberhard und Partner
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • DORTMUND
    • Accreditation
    • Molecular diagnosis of familial erythrocytosis (EGLN1, EGLN2, EPOR, VHL genes)
    • DRK Baden-Württemberg/ Hessen
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Baden-Württemberg
    • ULM
    • Accreditation
    • Molecular diagnosis of Congenital secondary polycythemia (VHL, EGLN1 and EPAS1 genes)
    • CHU de LIEGE - UniLab Lg
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • LIEGE
    • LIEGE
    • Accreditation
    • Molecular diagnosis of familial erythrocitosis (PHD2 and HIF2A gene)
    • Hosp. Pediátrico e Hosp. Covões - Centro Hospitalar e Universitário de Coimbra
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • PORTUGAL
    • CENTRO
    • COIMBRA
    • Molecular diagnosis of autosomal dominant secondary polycythemia (EGLN1 gene)
    • CHU d'Angers
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • ANGERS
    • Molecular diagnosis of autosomal dominant secondary polycythemia (EPAS1 gene)
    • CHU d'Angers
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • PAYS DE LA LOIRE
    • ANGERS
    • Molecular diagnosis of genetic polycythemia (EPOR, VHL, EGLN1, EPAS1 genes)
    • Hospital del Mar
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Molecular diagnosis of autosomal dominant secondary polycythemia (EGLN1 gene / sequence analysis entire coding region)
    • Genetaq
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis of Congenital Secondary Erythrocytosis due to Hemoglobin Variant with High Oxygen-Affinity (HBA1, HBA2 and HBB gene)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Molecular diagnosis of Congenital Secondary Erythrocytosis due to Defective Oxygen Sensing (VHL, EPAS1 and EGLN1 gene)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Molecular diagnosis of autosomal dominant secondary polycythemia (EGLN1 and EPAS1 genes: entire coding sequence)
    • Laboratorio de Genética Clínica, S.L.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES