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Caption : Accreditation =Accreditation
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    • ITALY
    • TOSCANA
    • FIRENZE
    • Accreditation
    • Molecular diagnosis of vitreoretinopathies (FZD4, LRP5, NDP, RS1, CYP4V2 and TSPAN12 gene)
    • Azienda Ospedaliero Universitaria Careggi
    • More information
    • UNITED KINGDOM
    • Greater Manchester
    • MANCHESTER
    • Accreditation
    • Molecular diagnosis of Retinal Degeneration (Multigene panel; 105 genes)
    • St Mary's Hospital
    • More information
    • DENMARK
    • Sjælland
    • GLOSTRUP
    • Accreditation
    • Molecular diagnosis of hereditary glaucoma (MYOC, OPTN, WDR36 genes: mutation screening ; CYP1B1: prenatal screening)
    • Kennedy Center
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of vitreoretinopathy (VCAN, COL2A1, FZD4, LRP5, NDP and TSPAN12 genes)
    • CHU Paris Centre - Hôpital Cochin
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Molecular diagnosis of Congenital retinal telangiectasia (Coats disease): complete sequencing of NDP gene
    • Universität Zürich
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of hereditary glaucoma (CYP1B1 gene)
    • Praxis für Humangenetik
    • More information
    • SWITZERLAND
    • Suisse Romande
    • SION
    • Molecular diagnosis of Hereditary Glaucoma (CYP1B1 and MYOC genes)
    • Institut de Recherche en Ophtalmologie - IRO
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of Coats disease (NDP gene / sequencing)
    • Centro Inmunológico de Alicante (CIALAB)
    • More information
    • POLAND
    • Poznan
    • POZNAN
    • Molecular diagnosis of hereditary glaucoma (MYOC, OPTN, CYP1B1 genes)
    • NZOZ Centrum Genetyki Medycznej Genesis
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of Glaucoma (Analysis of CYP1B1 and MYOC mutations)
    • NZOZ GENOMED
    • More information
    • SPAIN
    • Comunidad Valenciana
    • PATERNA
    • Molecular diagnosis of Coats disease (NDP gene / complete sequencing)
    • IMEGEN - Instituto de Medicina Genómica
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of Glaucoma (Analysis of CYP1B1 and MYOC mutations)
    • MEDGEN
    • More information
    • ITALY
    • LOMBARDIA
    • MILANO
    • Molecular diagnosis of hereditary glaucoma (CYP1B1 and MYOC/TIGR genes)
    • Ospedale Niguarda Ca' Granda
    • More information
    • ITALY
    • TOSCANA
    • SIENA
    • Molecular diagnosis of hereditary glaucoma (MYOC, OPTN genes)
    • Azienda Ospedaliera Universitaria Senese - Ospedale Santa Maria alle Scotte
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular diagnosis of hereditary glaucoma (MYOC and CYP1B1 gene sequencing)
    • Institute of Child Health
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Molecular diagnosis of Primary Glaucoma (MYOC, OPTN and CYP1B1 gene)
    • NIN - Netherlands Institute for Neuroscience
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of Coats disease (entire coding sequence of NDP gene)
    • Laboratorio de Genética Clínica, S.L.
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of congenital glaucoma (entire coding sequence of CYP1B1, OPTN, MYOC, WDR36 and LTBP2 genes)
    • Laboratorio de Genética Clínica, S.L.
    • More information
    • SPAIN
    • Madrid
    • MAJADAHONDA
    • Molecular diagnosis of hereditary glaucoma (sequencing of CYP1B1 and MYOC genes)
    • Genyca Innova
    • More information