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: Accreditation
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- FRANCE
- MIDI-PYRENEES
- TOULOUSE
- Molecular diagnosis of WAGR syndrome (WT1 and PAX6 genes)
- CHU de Toulouse - Hôpital Purpan
- More information
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- FRANCE
- MIDI-PYRENEES
- TOULOUSE
- Molecular diagnosis of aniridia and ocular related syndromes (PAX6 gene)
- CHU de Toulouse - Hôpital Purpan
- More information
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- GERMANY
- Nordrhein-Westfalen
- DÜSSELDORF
- Molecular and molecular cytogenetic diagnosis of WAGR syndrome (WT1, PAX6 genes). Deletion analysis for BDNF, FSHB, DCDC1, ELP4, PAX6, RCN1, WT1, HIPK3, LMO2, EHF and CD44 genes
- Heinrich-Heine Universität Düsseldorf
- More information
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- GERMANY
- Nordrhein-Westfalen
- DÜSSELDORF
- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- Heinrich-Heine Universität Düsseldorf
- More information
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- Molecular diagnosis of sporadic aniridia (PAX6 gene)
- Universitätsklinikum Hamburg-Eppendorf
- More information
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- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- Medizinisch Genetisches Zentrum München
- More information
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- SWITZERLAND
- Suisse Alémanique
- SCHWERZENBACH
- Cytogenetics and molecular cytogenetics diagnosis (FISH) of WAGR syndrome
- Universität Zürich
- More information
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- GERMANY
- Rheinland-Pfalz
- INGELHEIM AM RHEIN
- Molecular diagnosis of aniridia (PAX6 gene)
- Bioscientia Institut für Medizinische Diagnostik GmbH
- More information
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- GERMANY
- Rheinland-Pfalz
- INGELHEIM AM RHEIN
- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- Bioscientia Institut für Medizinische Diagnostik GmbH
- More information
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- BELGIUM
- OOST-VLAANDEREN
- GENT
- Molecular cytogenetic diagnosis of WAGR syndrome (11p13)
- Ghent University Hospital - UZGent
- More information
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- DENMARK
- Sjælland
- GLOSTRUP
- Prenatal and postnatal genetic diagnosis of aniridia (PAX6 gene: MLPA, Sequencing ; known mutations for prenatal)
- Kennedy Center
- More information
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- DENMARK
- Sjælland
- GLOSTRUP
- Molecular diagnosis of intellectual deficit due to microdeletions microduplications (SALSA MLPA kit P096)
- Kennedy Center
- More information
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- UNITED KINGDOM
- West Midlands
- BIRMINGHAM
- Molecular cytogenetic diagnosis of WAGR syndrome (by FISH analysis)
- Birmingham Women's NHS Foundation Trust
- More information
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- SWITZERLAND
- Suisse Alémanique
- SCHWERZENBACH
- Molecular diagnosis of Warg syndrome (11p13 deletion )
- Universität Zürich
- More information
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- UNITED KINGDOM
- Wiltshire
- SALISBURY
- Molecular diagnosis of Aniridia (PAX6 gene: full intragenic mutation screen)
- Salisbury District Hospital
- More information
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- UNITED KINGDOM
- Greater Manchester
- MANCHESTER
- Molecular cytogenetic diagnosis of WAGR syndrome (by FISH analysis)
- St Mary's Hospital
- More information
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- NETHERLANDS
- Noord-Holland
- AMSTERDAM
- Molecular diagnosis of Aniridia (PAX6 and SOX2 gene)
- AMC - Academisch Medisch Centrum
- More information
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- GERMANY
- Baden-Württemberg
- FREIBURG
- Molecular diagnosis of sporadic aniridia (PAX6 gene)
- Praxis für Humangenetik / Center for Human Genetics Freiburg
- More information
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- GERMANY
- Mecklenburg-Vorpommern
- ROSTOCK
- Molecular diagnosis of PAX6 gene-associated diseases (sequencing / MLPA)
- Institute of Molecular Diagnostics
- More information
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- GERMANY
- Baden-Württemberg
- HEIDELBERG
- Molecular cytogenetic diagnosis of WAGR syndrome (WT1, PAX6 genes)
- Universitätsklinikum Heidelberg
- More information
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- GERMANY
- Baden-Württemberg
- HEIDELBERG
- Molecular cytogenetic diagnosis of WAGR syndrome
- Universitätsklinikum Heidelberg
- More information
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- UNITED KINGDOM
- Wiltshire
- SALISBURY
- Molecular and molecular cytogenetic diagnosis of Aniridia and WAGR syndrome (PAX6 and WT1 analysis by FISH followed by sequencing)
- Salisbury District Hospital
- More information
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- GERMANY
- Hessen
- FRANKFURT AM MAIN
- Molecular diagnosis of aniridia (PAX6 gene)
- Zentrum für Humangenetik
- More information
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- GERMANY
- Hessen
- FRANKFURT AM MAIN
- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- Zentrum für Humangenetik
- More information
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- SPAIN
- Comunidad Valenciana
- PATERNA
- Preimplantation genetic diagnosis of aniridia (PAX6 gene)
- Sistemas Genómicos S.L.
- More information
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- GERMANY
- Baden-Württemberg
- TÜBINGEN
- Molecular diagnosis of PAX6 gene-associated diseases (sequencing)
- CeGaT GmbH
- More information
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- Molecular diagnosis of WAGR syndrome (WT1 deletion)
- CHU de Lyon-GH Est - Hospices Civils de Lyon
- More information
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- FRANCE
- LANGUEDOC-ROUSSILLON
- MONTPELLIER
- Cytogenetics preimplantation and post-natal diagnosis of WAGR syndrome (by FISH)
- CHU de Montpellier - Hôpital Arnaud de Villeneuve
- More information
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- FRANCE
- LORRAINE
- VANDOEUVRE-LES-NANCY
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- FRANCE
- ILE-DE-FRANCE
- PARIS
- Molecular cytogenetic diagnosis of WAGR syndrome (FISH analyses of WT1 and PAX6 genes)
- CHU Paris - Hôpital Necker - Enfants Malades
- More information
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- FRANCE
- PAYS DE LA LOIRE
- ANGERS
- Molecular cytogenetics diagnosis of WAGR syndrome (PAX6 and WT1 genes)
- CHU d'Angers
- More information
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- Molecular cytogenetic diagnosis of WAGR syndrome
- CHU d'Amiens - Centre de gynécologie et obstétrique
- More information
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- FRANCE
- CHAMPAGNE-ARDENNE
- REIMS
- Molecular cytogenetics diagnosis of WAGR syndrome
- CHU de Reims - Hôpital Maison Blanche
- More information
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- FRANCE
- HAUTE-NORMANDIE
- ROUEN
- Molecular cytogenetic diagnosis of WT1 gene deletion -associated diseases
- CHU de Rouen - Hôpital Charles Nicolle
- More information
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- Molecular cytogenetics diagnosis of WAGR syndrome
- Istituto CSS-Mendel
- More information
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- Molecular diagnosis of aniridia (PAX6 gene)
- Biotecnologie Avanzate Srl
- More information
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- Molecular diagnosis of WAGR syndrome (microsatellite analysis of 11p13 region for detecting microdeletions)
- Hospital Universitario Central de Asturias
- More information
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- ITALY
- FRIULI VENEZIA GIULIA
- UDINE
- Molecular diagnosis of sporadic aniridia (PAX6 gene)
- Azienda Ospedaliero-Universitaria "Santa Maria della Misericordia" di Udine
- More information
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- Molecular diagnosis of PAX6 gene-associated diseases
- Friedrich-Alexander-Universität Erlangen-Nürnberg
- More information
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- SPAIN
- País Vasco
- SAN SEBASTIÁN
- Molecular diagnosis of microdeletions syndromes (MLPA kit P245)
- Policlínica Gipúzcoa
- More information
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- SPAIN
- País Vasco
- SAN SEBASTIÁN
- Molecular diagnosis of microdeletions syndromes (MLPA kit P096)
- Policlínica Gipúzcoa
- More information
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- SPAIN
- País Vasco
- SAN SEBASTIÁN
- Molecular diagnosis of WAGR syndrome (array-CGH)
- Policlínica Gipúzcoa
- More information
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- Molecular cytogenetics diagnosis of WAGR syndrome.
- Prenatal Genetics S.L.
- More information
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- SPAIN
- Baleares
- PALMA DE MALLORCA
- Molecular diagnosis of microdeletion syndromes by MLPA
- Hospital Universitario Son Espases
- More information
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- Molecular diagnosis of WAGR syndrome (PAX6 and WT1 genes / detection of microdeletion of 11p13 region)
- Hospital Universitario Virgen del Rocío
- More information
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- GERMANY
- Nordrhein-Westfalen
- KÖLN
- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- Klinikum der Universität zu Köln
- More information
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- GERMANY
- Nordrhein-Westfalen
- KÖLN
- Molecular diagnosis of PAX6 gene-associated diseases
- Klinikum der Universität zu Köln
- More information
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- Molecular cytogenetics diagnosis of WAGR syndrome
- Instituto Nacional de Saúde Dr. Ricardo Jorge - Lisboa
- More information
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- SPAIN
- Comunidad Valenciana
- PATERNA
- Molecular diagnosis of isolated aniridia (PAX6 gene)
- Sistemas Genómicos S.L.
- More information
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- Molecular diagnosis of WAGR syndrome (MLPA)
- Hospital Universitario Miguel Servet
- More information
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- GERMANY
- Niedersachsen
- OSNABRÜCK
- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- Praxis Dres. Gencik
- More information
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- GERMANY
- Niedersachsen
- OSNABRÜCK
- Molecular diagnosis of PAX6 gene-associated diseases (sequencing / MLPA)
- Praxis Dres. Gencik
- More information
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- GERMANY
- Sachsen
- WEIßWASSER
- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- Praxis Dr. Mato Nagel
- More information
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- Molecular diagnosis of aniridia (PAX6 and WT1 genes)
- Fundación Jiménez Díaz
- More information
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- Molecular diagnosis of aniridia (PAX6 gene)
- Praxis für Humangenetik
- More information
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- SWITZERLAND
- Suisse Romande
- SION
- Molecular diagnosis of Aniridia (PAX6 gene)
- Institut de Recherche en Ophtalmologie - IRO
- More information
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- Molecular diagnosis of WAGR syndrome (MLPA)
- Leto Maternity Hospital
- More information
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- Molecular diagnosis of WAGR syndrome by MLPA
- Mitera General, Maternity and Children's Hospital
- More information
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- Molecular diagnosis of WAGR syndrome (WT1 and PAX6 genes): deletion/duplication analysis
- CGC Genetics / Centro de Genética Clínica
- More information
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- Molecular cytogenetics diagnosis of WAGR syndrome (PAX6 and WT1 genes)
- Haukeland University Hospital
- More information
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- Molecular cytogenetics diagnosis of aniridia (PAX6 gene)
- Haukeland University Hospital
- More information
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- SPAIN
- País Vasco
- BARAKALDO
- Molecular Diagnosis of WAGR Syndrome . Sequencing of the gene WT1.
- Hospital Universitario Cruces - Osakidetza
- More information
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- Molecular cytogenetic diagnosis of WAGR syndrome
- Azienda Ospedaliera Universitaria Anna Meyer
- More information
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- UNITED KINGDOM
- Cambridgeshire
- CAMBRIDGE
- Cytogenetic diagnosis of WAGR syndrome
- Cambridge University Hospitals NHS Foundation Trust
- More information
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- GERMANY
- Nordrhein-Westfalen
- MÜNSTER
- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- Universitätsklinikum Münster
- More information
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- SWEDEN
- Stockholms läns landsting
- STOCKHOLM
- Molecular diagnosis of aniridia (PAX6 gene)
- Karolinska University Hospital - Solna
- More information
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- SWEDEN
- Stockholms läns landsting
- STOCKHOLM
- Molecular cytogenetics diagnosis of WAGR syndrome (PAX6 and WT1 genes)
- Karolinska University Hospital - Solna
- More information
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- Molecular cytogenetic diagnosis of WAGR syndrome
- Medizinische Fakultät Carl Gustav Carus der TU Dresden
- More information
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- GERMANY
- Rheinland-Pfalz
- MAINZ
- MLPA analysis of microdeletion syndrome regions
- Universitätsmedizin Mainz
- More information
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- Molecular diagnosis of PAX6-related aniridia (PAX6 gene)
- NZOZ Centrum Genetyki Medycznej Genesis
- More information
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- UNITED KINGDOM
- Greater London
- LONDON
- Cytogenetic diagnosis of WAGR syndrome (by FISH at 11p13)
- Guy's Hospital
- More information
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- FRANCE
- PROVENCE-ALPES-COTE D'AZUR
- MARSEILLE
- Molecular cytogenetics diagnosis of WAGR syndrome
- CHU de Marseille - Hôpital de la Timone
- More information
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- SPAIN
- Comunidad Valenciana
- PATERNA
- Molecular diagnosis of aniridia. PAX6 gene (complete sequencing).
- IMEGEN - Instituto de Medicina Genómica
- More information
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- Molecular diagnosis of microdeletion and microduplication syndromes by MLPA
- Gemeinschaftspraxis für Humangenetik
- More information
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- Molecular diagnosis of WAGR syndrome: diagnostic and prenatal testing (locus 11p13 / MLPA)
- Hospital Clínico San Carlos
- More information
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- Molecular diagnosis of chromosomal anomalies (array-CGH)
- NIMGenetics
- More information
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- Molecular cytogenetics diagnosis of WAGR syndrome (11p13-14): deletion/duplication analysis by MLPA, FISH and prenatal testing
- Laboratório de Análises Clínicas Dr. Joaquim Chaves
- More information
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- FRANCE
- ILE-DE-FRANCE
- BONDY
- Cytogenetic diagnosis of WAGR syndrome (FISH analysis)
- CHU Paris Seine-Saint-Denis - Hôpital Jean Verdier
- More information
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- Molecular cytogenetic diagnosis of WAGR syndrome
- Azienda Ospedaliera S. Camillo-Forlanini
- More information
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- Molecular cytogenetics diagnosis of WAGR syndrome
- Presidio Ospedaliero "Vito Fazzi" - ASL LE
- More information
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- Molecular diagnosis of WAGR syndrome
- Azienda Ospedaliera Universitaria Senese - Ospedale Santa Maria alle Scotte
- More information
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- Molecular cytogenetics diagnosis of WAGR syndrome
- Università degli Studi di Milano
- More information
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- Molecular cytogenetics diagnosis of WAGR syndrome
- Azienda Ospedaliera Universitaria "Federico II"
- More information
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- Cytogenetics diagnosis of WAGR syndrome (11p13 deletion)
- Azienda Ospedaliera Universitaria Integrata di Verona - Ospedale Borgo Roma
- More information
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- Molecular cytogenetic diagnosis of WAGR syndrome
- A.O.U. Ospedale di Circolo e Fondazione Macchi - Università dell'Insubria
- More information
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- Cytogenetics diagnosis of WAGR syndrome
- Azienda Ospedaliera Santa Croce e Carle
- More information
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- Molecular diagnosis of isolated aniridia (PAX6 gene)
- Universitat de Barcelona. Facultat de Biologia
- More information
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- GERMANY
- Mecklenburg-Vorpommern
- ROSTOCK
- Molecular diagnosis of anophthalmia and/or microphthalmia (PAX6 and SOX2 genes)
- Universitätsklinikum Rostock
- More information
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- SPAIN
- Extremadura
- BADAJOZ
- Molecular cytogenetics diagnosis of chromosome anomalies
- Hospital Perpetuo Socorro
- More information
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- Molecular cytogenetics diagnosis of WAGR syndrome
- Complejo Hospitalario Universitario A Coruña
- More information
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- Cytogenetic molecular diagnosis of WAGR syndrome
- Centro de Investigación sobre Anomalías Congénitas
- More information
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- Molecular cytogenetic diagnosis of WAGR syndrome
- Azienda Ospedaliera Universitaria di Perugia Santa Maria della Misericordia
- More information
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- Molecular diagnosis of Microdeletion syndromes by MLPA and FISH analysis
- Eskisehir Osmangazi University Medical Faculty
- More information
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- GERMANY
- Nordrhein-Westfalen
- MÜNSTER
- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- KfH Kuratorium für Dialyse und Nierentransplantation e.V.
- More information
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- GERMANY
- Baden-Württemberg
- HEIDELBERG
- Molecular diagnosis of WT1 gene-associated diseases (WAGR syndrome, Denys Drash, Frasier-Syndrom, Wilms tumor and others)
- Universitätsklinikum Heidelberg
- More information
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- Molecular diagnosis of intellectual deficit syndromes (MLPA kits P064 & P096)
- The Children's Memorial Health Institute CMHI (IP-CZD)
- More information
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- Molecular diagnosis of microdeletions syndromes (MLPA kit P245 & P297)
- The Children's Memorial Health Institute CMHI (IP-CZD)
- More information
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- Molecular diagnosis of WAGR syndrome (aCGH)
- Genetadi Biotech S.L.
- More information
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- MLPA analysis of microdeletion syndromes
- Faculdade de Medicina da Universidade de Coimbra
- More information
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- SPAIN
- Comunidad Valenciana
- PATERNA
- Preimplantation genetic diagnosis of aniridia (PAX6 gene)
- Iviomics SL
- More information
