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Caption : Accreditation =Accreditation
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    • UNITED KINGDOM
    • Greater Manchester
    • MANCHESTER
    • Accreditation
    • Molecular diagnosis of Retinal Degeneration (Multigene panel; 105 genes)
    • St Mary's Hospital
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Accreditation
    • Molecular diagnosis of corneal dystrophy (COL8A2, TGFBI, VSX1, CHST6, KRT3, UBIAD1, KRT12, TACSTD2, CYP4V2, SOD1, ZEB1 and SLC4A11 genes) : genotyping by arrayed primer extension (APEX)
    • Asper Biotech Ltd.
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of TGFBI gene-associated corneal dystrophies
    • Centogene AG
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of corneal dystrophy (TGFBI CHST6, ZEB1, VSX1 genes)
    • CHU Paris Centre - Hôpital Cochin
    • More information
    • ITALY
    • VENETO
    • COSTOZZA DI LONGARE
    • Molecular diagnosis of corneal dystrophy (TGFBI gene)
    • B.I.R.D. Foundation
    • More information
    • GERMANY
    • Sachsen-Anhalt
    • HALLE (SAALE)
    • Molecular diagnosis of corneal dystrophies (CHST6, GSN, KRT3, KRT12, TACSTD2, TGFBI, UBIAD1 genes)
    • Universitätsklinikum Halle (Saale)
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of corneal dystrophy (COL8A, TGFBI, VSX1, CHST6, KRT3, KRT12, GSN, TACSTD2, CYP4V2, ZEB1, SLC4A11, UBIAD1 genes / Chip CD)
    • Fundación Jiménez Díaz
    • More information
    • SWITZERLAND
    • Suisse Romande
    • SION
    • Molecular diagnosis of Corneal Dystrophy (BIGH3/TGFBI, KRT3, KRT12, Gelsolin and CYP4V2 genes)
    • Institut de Recherche en Ophtalmologie - IRO
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Molecular diagnosis of TGFBI gene-associated corneal dystrophies
    • Universitätsmedizin Rostock
    • More information
    • SPAIN
    • Madrid
    • SAN SEBASTIÁN DE LOS REYES
    • Molecular diagnosis of corneal dystrophy (TGFBI gene: exons 4, 11, 12, 13, 14 - mutations in exon 12 - entire coding sequence)
    • Laboratorio de Genética Clínica, S.L.
    • More information