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33 Result(s)

Result(s)sorted by
Speciality(ies)/objective(s)
(32)
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Technique(s)
(5)
Purpose(s)
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(32)
Quality management
(9)
(17)
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Result(s)sorted by

Caption : Accreditation =Accreditation
;

    • Molecular diagnosis of Cerebral Cavernous Malformations (KRIT1, CCM2, PDCD10 genes)
    • Erasmus MC, Faculteitsgebouw
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NETHERLANDS
    • Zuid-Holland
    • ROTTERDAM
    • Accreditation
    • Molecular diagnosis of cerebral cavernous malformations (CCM2, KRIT1, PDCD10 genes: sequencing / MLPA)
    • Universitätsklinikum Regensburg
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • GERMANY
    • Bayern
    • REGENSBURG
    • Accreditation
    • Molecular diagnosis of Cerebral Cavernous Malformations by sequence analysis of the entire coding regions of gene(s) (Genes: CCM2, KRIT1, PDCD10)
    • Ninewells Hospital and Medical School
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • UNITED KINGDOM
    • Tayside
    • DUNDEE
    • Accreditation
    • Molecular diagnosis of Cerebral cavernous malformations (KRIT1 gene)
    • Université Catholique de Louvain - UCL
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • BELGIUM
    • ARRONDISSEMENT BRUSSELS-CAPITAL
    • BRUXELLES
    • Accreditation
    • Molecular diagnosis of cerebral cavernous malformations (CCM2, KRIT1, PDCD10 genes)
    • Centogene AG
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of cerebral cavernous malformations (CCM2, KRIT1, PDCD10 genes)
    • laboratoriumsmedizin köln - Dres. med. Wisplinghoff und Kollegen
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • KÖLN
    • Accreditation
    • Molecular diagnosis of Familial Cerebral Cavernous Malformations type 1, 2 and 3 (KRIT1, CCM2 and PDCD10 gene)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Molecular diagnosis of cerebral cavernous malformations (CCM2, KRIT1, PDCD10 genes)
    • Praxis für Humangenetik Freiburg
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of hereditary cerebral cavernous malformation (KRIT1, CCM2, PDCD10 genes)
    • Reference Laboratory Genetics
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Cataluña
    • L'HOSPITALET DE LLOBREGAT
    • Accreditation
    • Molecular diagnosis of cerebral cavernous malformations (CCM2, KRIT1, PDCD10 genes)
    • Pränatalmedizin München
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of cerebral cavernous malformations (CCM2, PDCD10 and KRIT1 genes)
    • CHU Paris-GH St-Louis Lariboisière F.Widal - Hôpital Lariboisière
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of cerebral cavernous malformations(KRIT1 gene: sequencing and mutations 1363C>T, dG699 ,Q698X; CCM2, PDCD10 genes: MLPA)
    • Genetaq
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • SPAIN
    • Andalucía
    • MÁLAGA
    • Molecular diagnosis of cerebral cavernous malformations (CCM2, KRIT1, PDCD10 genes: sequencing / MLPA)
    • Institut für Humangenetik der Universitätsmedizin Greifswald
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • GREIFSWALD
    • Molecular diagnosis of hereditary cerebral cavernous malformation (entire coding sequence of CCM2, KRIT1 and PDCD10 genes)
    • Lorgen G.P.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region
    • More information
    • SPAIN
    • Andalucía
    • ARMILLA
    • Molecular diagnosis of hereditary cerebral cavernous malformation (KRIT1, CCM2 genes)
    • Sistemas Genómicos S.L.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of cerebral cavernous malformations (CCM2, KRIT1, PDCD10 genes)
    • Institut für Klinische Genetik Bonn
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • GERMANY
    • Nordrhein-Westfalen
    • BONN
    • Molecular diagnosis of hereditary cerebral cavernous malformation (KRIT1, CCM2, PDCD10 genes)
    • IMEGEN - Instituto de Medicina Genómica
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of hereditary cerebral cavernous malformation (KRIT1, CCM2, PDCD10 genes)
    • Fundación Jiménez Díaz
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of hereditary cerebral cavernous malformation (KRIT1, MGC4607, PDCD10 genes)
    • Azienda Ospedaliero-Universitaria San Giovanni Battista di Torino
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • PIEMONTE
    • TORINO
    • Molecular diagnosis of hereditary cerebral cavernous malformation (aCGH)
    • Genetadi Biotech S.L.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • País Vasco
    • DERIO
    • Molecular diagnosis of hereditary cerebral cavernous malformation (KRIT1, CCM2, PDCD10)
    • Hospital Universitari General Vall d'Hebron
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Molecular diagnosis of hereditary cerebral cavernous malformation (KRIT1 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 hereditary cerebral cavernous malformation (KRIT1, CCM2, PDCD10 genes / sequencing, MLPA)
    • Centro Inmunológico de Alicante (CIALAB)
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Technical procedure(s) : MLPA based techniques
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of cerebral cavernous malformations (KRIT1/CCM1, MGC4607/CCM2, PDCD10/CCM3 genes)
    • Ospedale Niguarda Ca' Granda
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of cerebral cavernous malformations (KRIT1, MGC4607 and PDCD10 genes)
    • IRCCS Ospedale Casa Sollievo della Sofferenza - Polamb. Giovanni Paolo II
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • PUGLIA
    • SAN GIOVANNI ROTONDO
    • Anatomo-pathological diagnosis of familial cerebral cavernous malformations
    • CHU de Caen - Hôpital de la Côte de Nacre
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Pathology
    • More information
    • FRANCE
    • BASSE-NORMANDIE
    • CAEN
    • Molecular diagnosis of cerebral cavernous malformations (tipo 1, 2, and 3) (PDCD10, CCM2, KRIT1 genes)
    • Istituto Neurologico Mediterraneo - IRCCS Neuromed
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • MOLISE
    • POZZILLI
    • Molecular diagnosis of cerebral cavernous malformations. KRIT1/CCM1, CCM2, PDCD10/CCM3 genes
    • Hospital Universitario Virgen Macarena
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Andalucía
    • SEVILLA
    • Molecular diagnosis of hereditary cerebral cavernous malformation (deletions by MLPA analysis and entire coding sequence of KRIT1, CCM2 and PDCD10 genes)
    • Laboratorio de Genética Clínica, S.L.
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • Objective(s) : Sequence analysis: entire coding region, Deletion / Duplication analysis
    • Technical procedure(s) : MLPA based techniques
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of hereditary cerebral cavernous malformation (sequencing of KRT1, CCM2 and PDCD10 genes)
    • Genyca Innova
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Madrid
    • MAJADAHONDA
    • Molecular diagnosis of cerebral cavernous malformation (KRIT1 gene)
    • IRCCS Istituto G. Gaslini - Ospedale Pediatrico
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • ITALY
    • LIGURIA
    • GENOVA
    • Preimplantation genetic diagnosis of hereditary cerebral cavernous malformation (KRIT1 gene)
    • Igenomix Spain
    • Purpose(s) : Pre-implantation diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of familial cerebral cavernous malformation (CCM2, KRIT1, PDCD10 genes)
    • Bioarray
    • Purpose(s) : Post-natal diagnosis
    • Specialty(ies) : Molecular genetics
    • More information
    • SPAIN
    • Comunidad Valenciana
    • ELCHE