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Caption : Accreditation =Accreditation
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    • FRANCE
    • MIDI-PYRENEES
    • TOULOUSE
    • Accreditation
    • Molecular diagnosis of early-onset glaucoma (PITX2 and FOXC1 genes)
    • CHU de Toulouse - Hôpital Purpan
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of Rieger syndrome (FOXC1, PITX2 genes)
    • Medizinisch Genetisches Zentrum München
    • More information
    • GERMANY
    • Rheinland-Pfalz
    • INGELHEIM AM RHEIN
    • Accreditation
    • Molecular diagnosis of hereditary glaucoma (CYP1B1 and MYOC genes)
    • Bioscientia Institut für Medizinische Diagnostik GmbH
    • More information
    • DENMARK
    • Sjælland
    • GLOSTRUP
    • Accreditation
    • Molecular diagnosis of hereditary glaucoma (MYOC, OPTN, WDR36 genes: mutation screening ; CYP1B1: prenatal screening)
    • Kennedy Center
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of Rieger syndrome (FOXC1, PITX2 genes)
    • Zentrum für Humangenetik Mannheim
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of Rieger syndrome (FOXC1, PITX2 genes)
    • Praxis für Humangenetik Freiburg
    • More information
    • UNITED KINGDOM
    • Avon
    • BRISTOL
    • Accreditation
    • Molecular diagnosis of Rieger syndrome (FOXC1, PITX2 genes)
    • Southmead Hospital
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of hereditary glaucoma (CYP1B1, LTBP3, MYOC, OPTN and WDR36 genes)
    • Centogene AG
    • More information
    • GERMANY
    • Baden-Württemberg
    • TÜBINGEN
    • Accreditation
    • Molecular diagnosis of Rieger syndrome (FOXC1 gene: sequencing)
    • CeGaT GmbH
    • More information
    • GERMANY
    • Bayern
    • ERLANGEN
    • Molecular diagnosis of hereditary glaucoma (MYOC and CYP1B1 genes)
    • Universitätsklinikum Erlangen
    • More information
    • GERMANY
    • Niedersachsen
    • OSNABRÜCK
    • Molecular diagnosis of Rieger syndrome (PITX2 gene, FOXC1 gene on request)
    • Praxis Dres. Gencik
    • More information
    • GERMANY
    • Sachsen
    • WEIßWASSER
    • Molecular diagnosis of hereditary glaucoma (CYP1B1 and MYOC genes)
    • Praxis Dr. Mato Nagel
    • 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 Axenfeld-Rieger syndrome and anomalies (FOXC1, PITX2 genes / sequencing, MLPA)
    • Centro Inmunológico de Alicante (CIALAB)
    • More information
    • POLAND
    • Poznan
    • POZNAN
    • Molecular diagnosis of Rieger-Axenfeld syndrome (PTX2 gene: sequence analysis)
    • NZOZ Centrum Genetyki Medycznej Genesis
    • 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 Rieger's anomaly (PITX2 gene - entire coding sequence)
    • 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
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Molecular diagnosis of primary congenital glaucoma
    • Universitätsmedizin Rostock
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of Axenfeld-Rieger syndrome and Rieger's anomaly (PITX2, FOXC1 genes)
    • Hospital Universitario Ramón y Cajal
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of hereditary glaucoma (CYP1B1, MYOC, LTBP2 genes)
    • Hospital Universitario Ramón y Cajal
    • 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 Rieger-Axenfeld anomaly (PITX2 and FOXC1 genes)
    • 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
    • SPAIN
    • País Vasco
    • DERIO
    • Molecular diagnosis of Rieger's anomaly (aCGH)
    • Genetadi Biotech S.L.
    • More information