Caption
: Accreditation
=
; Certification
=
;
-
- BELGIUM
- OOST-VLAANDEREN
- GENT
- Molecular diagnosis of optic atrophy type 1 (OPA1 gene)
- Ghent University Hospital - UZGent
- More information
-
- FRANCE
- ILE DE FRANCE
- SAINT OUEN L'AUMONE
- Biochemical diagnosis of 3-methylglutaconicaciduria
- Laboratoire Cerba
- More information
-
- Molecular diagnosis of autosomal dominant optic atrophy (OPA1 gene)
- Medizinisch Genetisches Zentrum München
- More information
-
- NETHERLANDS
- Noord-Holland
- AMSTERDAM
- Molecular diagnosis of Optic atrophy, type 1 (OPA1 gene)
- AMC - Academisch Medisch Centum
- More information
-
- UNITED KINGDOM
- South Glamorgan
- CARDIFF
- Molecular diagnosis of Autosomal Dominant Optic Atrophy, OPA1 type (by direct sequence analysis of 3q28-q29)
- University Hospital of Wales NHS Trust
- More information
-
- UNITED KINGDOM
- South Yorkshire
- SHEFFIELD
- Biochemical diagnosis of fatty acid oxidation defects and organic acidaemias (Analyte: Acyl carnitine by tandem MS)
- Sheffield Children's NHS Foundation Trust
- More information
-
- UNITED KINGDOM
- South Yorkshire
- SHEFFIELD
- Biochemical diagnosis of Organic acidaemias (Analyte: Qualitative organic acids)
- Sheffield Children's NHS Foundation Trust
- More information
-
- UNITED KINGDOM
- Tyne & Wear
- NEWCASTLE UPON TYNE
- Biochemical diagnosis of fatty acid oxidation defects and organic acidaemias (Analyte: Acyl carnitine by tandem MS)
- Royal Victoria Infirmary
- More information
-
- UNITED KINGDOM
- Tyne & Wear
- NEWCASTLE UPON TYNE
- Biochemical diagnosis of Organic acidaemias (Analyte: Organic acid specific quantitation, usually by stable isotope analysis)
- Royal Victoria Infirmary
- More information
-
- UNITED KINGDOM
- Tyne & Wear
- NEWCASTLE UPON TYNE
- Biochemical diagnosis of Organic acidaemias (Analyte: Qualitative organic acids)
- Royal Victoria Infirmary
- More information
-
- UNITED KINGDOM
- West Yorkshire
- LEEDS
- Molecular diagnosis of Optic Atrophy 1 (partial coding region sequencing and dosage analysis, OPA1 gene)
- St James's University Hospital
- More information
-
- BULGARIA
- South-West region
- SOFIA
- Biochemical diagnosis of organic aciduria using GCMS analysis
- University hospital of Obstetrics and Gynecology
- More information
-
- Molecular diagnosis of autosomal dominant optic atrophy (OPA1 gene) : genotyping by arrayed primer extension (APEX)
- Asper Biotech Ltd.
- More information
-
- Molecular diagnosis of Costeff Optic Atrophy Syndrome (OPA3, Mutation analysis, Carrier screening)
- Carmel Medical Center
- More information
-
- Molecular diagnosis of Costeff Optic Atrophy Syndrome (OPA3, Mutation analysis, Carrier screening)
- Hadassah University Hospital
- More information
-
- ISRAEL
- ISRAEL
- PETAH TIKVA
- Molecular diagnosis of Costeff Optic Atrophy syndrome (OPA3, Mutation analysis, Carrier screening)
- Rabin Medical Center
- More information
-
- SPAIN
- Galicia
- SANTIAGO DE COMPOSTELA
- molecular diagnosis of septooptic dysplasia. HESX1 gene
- Fundación Pública Galega de Medicina Xenómica
- More information
-
- Molecular diagnosis of Costeff Optic Atrophy Syndrome (OPA3, Mutation analysis, Carrier screening)
- The Bnai Zion Medical Center, Technion-Rappaport Faculty of Medicine
- More information
-
- Molecular diagnosis of Costeff Optic Atrophy Syndrome (3MGA) (OPA3, Mutation analysis, Carrier screening, PGD)
- Sheba Medical Center
- More information
-
- Molecular diagnosis of septooptic dysplasia. HESX1 gene.
- GENETAQ
- More information
-
- DENMARK
- Sjælland
- GLOSTRUP
- Prenatal and postnatal molecular diagnosis of type OPA1 optic atrophy (OPA1 gene: sequence analysis; carrier screening)
- Kennedy Center
- More information
-
- Diagnosis of organic acidurias : quantitative organic acid analysis (GC/MS)
- United Laboratories - Tartu University Hospital
- More information
-
- FRANCE
- ILE DE FRANCE
- PARIS
- Molecular diagnosis of combined pituitary hormon deficiency, syndromic or non-syndromic (HESX1, LHX3, LHX4, POU1F1, PROP1 and SOX2 genes)
- CHU Hôpital d'Enfants Armand-Trousseau
- More information
-
- FRANCE
- NORD-PAS DE CALAIS
- LILLE
- Biochemical diagnosis of 3-methylglutaconicaciduria
- CHRU de Lille - Centre de biologie et pathologie
- More information
-
- GERMANY
- Baden-Württemberg
- FREIBURG
- Molecular diagnosis of septooptic dysplasia (HESX1 gene)
- Praxis für Humangenetik / Center for Human Genetics Freiburg
- More information
-
- GERMANY
- Bayern
- REGENSBURG
- Molecular diagnosis of septooptic dysplasia (HESX1 gene)
- Universitätsklinikum Regensburg
- More information
-
- GERMANY
- Bayern
- REGENSBURG
- Molecular diagnosis of autosomal dominant optic atrophy (OPA1 gene)
- Universitätsklinikum Regensburg
- More information
-
- GERMANY
- Niedersachsen
- OSNABRÜCK
- Molecular diagnosis of septooptic dysplasia (HESX1 gene)
- Zentrum für medizinische Genetik Osnabrück
- More information
-
- ITALY
- PUGLIA
- SAN GIOVANNI ROTONDO
- Molecular diagnosis of septooptic dysplasia
- IRCCS Ospedale Casa Sollievo della Sofferenza
- More information
-
- SPAIN
- Andalucía
- BARAKALDO
- Molecular Diagnosis of Septooptic dysplasia. Sequentiation of the gene HESX1.
- Hospital de Cruces - Osakidetza
- More information
-
- Biochemical diagnosis of 3-methylglutaconicaciduria
- Corporació Sanitària Clínic
- More information
-
- Biochemical diagnosis of 3-methylglutaconic aciduria, type 3
- Corporació Sanitària Clínic
- More information
-
-
- FRANCE
- AQUITAINE
- BORDEAUX
- Biochemical diagnosis of 3-methylglutaconic aciduria types 1, 2, 3 and 4
- CHU de Bordeaux - Hôpital Pellegrin
- More information
-
- FRANCE
- BASSE NORMANDIE
- CAEN
- Biochemical diagnosis of 3-methylglutaconicaciduria
- CHU Hôpital de la Côte de Nacre
- More information
-
- FRANCE
- HAUTE NORMANDIE
- ROUEN
- Biochemical diagnosis of 3-methylglutaconic aciduria types 1, 2, 3 and 4
- CHU Hôpital Charles Nicolle
- More information
-
- FRANCE
- ILE DE FRANCE
- PARIS
- Biochemical diagnosis of 3-methylglutaconicaciduria
- CHU de Paris - Hôpital Robert Debré
- More information
-
- FRANCE
- ILE DE FRANCE
- PARIS
- Biochemical diagnosis of 3-methylglutaconicaciduria
- Hopital Necker - Enfants Malades
- More information
-
- FRANCE
- LANGUEDOC-ROUSSILLON
- MONTPELLIER
- Molecular diagnosis of septooptic dysplasia (HESX1 gene)
- CHRU de Montpellier - Hôpital Lapeyronie
- More information
-
- FRANCE
- PAYS DE LOIRE
- ANGERS
- Biochemical diagnosis of 3-methylglutaconicaciduria
- CHU d'Angers
- More information
-
- FRANCE
- PAYS DE LOIRE
- ANGERS
- Molecular diagnosis of optic atrophy, dominant type (OPA1 gene)
- CHU d'Angers
- More information
-
- FRANCE
- PAYS DE LOIRE
- ANGERS
- Molecular diagnosis of methylglutaconicaciduria type III (OPA3 gene)
- CHU d'Angers
- More information
-
- FRANCE
- PAYS DE LOIRE
- ANGERS
- Molecular diagnosis of autosomal dominant optic atrophy and cataract (OPA3 gene)
- CHU d'Angers
- More information
-
- FRANCE
- PROVENCE-ALPES-COTE D'AZUR
- MARSEILLE
- Molecular diagnosis of septooptic dysplasia (HESX1 gene)
- Hôpital de la Conception - AP-HM
- More information
-
- FRANCE
- PROVENCE-ALPES-COTE D'AZUR
- NICE
-
- Biochemical diagnosis of 3-methylglutaconic acidurias
- Groupement Hospitalier Universitaire - Centre de Biologie et Pathologie Est
- More information
-
- FRANCE
- RHONE-ALPES
- GRENOBLE
- Biochemical diagnosis of 3-methylglutaconicaciduria
- CHU de Grenoble - Hôpital de la Tronche
- More information
-
- GERMANY
- Baden-Württemberg
- HEIDELBERG
- Biochemical diagnosis of 3-methylglutaconic aciduria (organic acids in urine)
- Universitätsklinikum Heidelberg
- More information
-
- GERMANY
- Baden-Württemberg
- TÜBINGEN
- Molecular diagnosis of autosomal dominant optic atrophy type Kjer (OPA1 gene)
- Universitätsklinik Tübingen
- More information
-
- GERMANY
- Rheinland-Pfalz
- LUDWIGSHAFEN
- Molecular diagnosis of autosomal dominant optic atrophy (OPA1 gene)
- Klinikum der Stadt Ludwigshafen gGmbH
- More information
-
-
- ITALY
- EMILIA ROMAGNA
- BOLOGNA
- Molecular diagnosis of septooptic dysplasia (HESX1 gene)
- Azienda Ospedaliera di Bologna - Policlinico S. Orsola-Malpighi
- More information
-
- Biochemical diagnosis of 3-methylglutaconicaciduria
- IRCCS Ospedale Pediatrico Bambino Gesù
- More information
-
- Molecular diagnosis of septooptic dysplasia (HESX1 gene)
- Università degli Studi di Brescia - Azienda Ospedaliera Spedali Civili
- More information
-
- Molecular diagnosis of multiple congenital pituitary deficiency
- Fondazione IRCCS Ospedale Maggiore Policlinico Mangiagalli e Regina Elena
- More information
-
- Biochemical diagnosis of 3-methylglutaconic aciduria, type 3
- Ospedale dei Bambini ''Vittore Buzzi"
- More information
-
- Biochemical diagnosis of 3-methylglutaconicaciduria
- Ospedale Regionale per le Microcitemie - ASL 8
- More information
-
- Biochemical diagnosis of 3-methylglutaconic aciduria
- Azienda Ospedaliera Universitaria Anna Meyer
- More information
-
-
- Molecular diagnosis of optic atrophy and cataract, autosomal dominant
- Policlinico "Le Scotte"
- More information
-
- Biochemical diagnosis of 3-methylglutaconicaciduria
- Instituto de Genética Médica Jacinto Magalhães
- More information
-
- SPAIN
- Cataluña
- ESPLUGUES DE LLOBREGAT
- Biochemical diagnosis of optic atrophy.
- Hospital Universitari Sant Joan de Déu
- More information
-
- SPAIN
- Cataluña
- ESPLUGUES DE LLOBREGAT
- Biochemical diagnosis of 3-methylglutaconic aciduria, type 3.
- Hospital Universitari Sant Joan de Déu
- More information
-
- Biochemical and molecular diagnsosis of the 3-methylglutaconic aciduria. AUH, OPA3 genes
- Universidad Autónoma de Madrid. Facultad de Ciencias
- More information
-
- Molecular diagnosis of the septooptic dysplasia. HESX1 gene
- Hospital Universitario La Paz
- More information
-
- Molecular diagnosis of optic atrophy. OPA1 gen
- Universidad Autónoma de Madrid. Facultad de Medicina
- More information
-
- SWEDEN
- Stockholms läns landsting
- STOCKHOLM
- Molecular diagnosis of mitochondrial diseases (mtDNA/POLG/Twinkle)
- Karolinska University Hospital
- More information
-
- UNITED KINGDOM
- Oxfordshire
- OXFORD
- Molecular diagnosis of Mitochondrial diseases (POLG, PEO1, DGUOK, ANT1 & MPV17 genes)
- Churchill Hospital, Oxford Radcliffe Hospitals NHS Trust
- More information
-
- UNITED KINGDOM
- Strathclyde
- GLASGOW
- Biochemical diagnosis of fatty acid oxidation defects and organic acidaemias (Analyte: Acyl carnitine by tandem MS)
- Royal Hospital for Sick Children - Yorkhill
- More information
-
- UNITED KINGDOM
- Strathclyde
- GLASGOW
- Biochemical diagnosis of Organic acidaemias (Analyte: Qualitative organic acids)
- Royal Hospital for Sick Children - Yorkhill
- More information
