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Caption : Accreditation =Accreditation
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    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of FGFR-associated skeletal dysplasias / craniosynostosis syndromes (FGFR1, FGFR2 and FGFR3 genes: sequencing, MLPA)
    • Pränatalmedizin München
    • More information
    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of Carpenter syndrome (RAB23 gene: sequencing)
    • Pränatalmedizin München
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Accreditation
    • Search of genomic DNA duplications and/or deletions by array-CGH
    • Centre Hospitalier Universitaire Vaudois CHUV
    • More information
    • GERMANY
    • Bayern
    • WÜRZBURG
    • Accreditation
    • Molecular diagnosis of Carpenter syndrome (RAB23 gene)
    • Universität Würzburg - Biozentrum
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Craniosynostosis 3 (TCF12 gene)
    • Great Ormond Street Hospital for Children, York House
    • More information
    • UNITED KINGDOM
    • Greater London
    • LONDON
    • Accreditation
    • Molecular diagnosis of Craniosynostosis 4 (ERF gene)
    • Great Ormond Street Hospital for Children, York House
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Accreditation
    • Search of genomic DNA duplications and/or deletions by CGH arrays / chromosomal microarrays
    • Universität Zürich
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of Carpenter Syndrome (RAB23 gene)
    • VUmc - VU medisch centrum
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Multiple Congenital Anomalies (SNP-array)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • UNITED KINGDOM
    • Oxfordshire
    • OXFORD
    • Accreditation
    • Molecular diagnosis of Carpenter syndrome (RAB23 gene)
    • The Churchill Hospital
    • More information
    • ESTONIA
    • Tartu
    • TARTU
    • Accreditation
    • Molecular diagnosis of skeletal dysplasia (APEX and sequencing: FGFR3, FGFR2, COL2A1, SLC26A2, ALPL, ROR2, ESCO2, CHST3 and SOX9 genes)
    • Asper Biotech Ltd.
    • More information
    • SWEDEN
    • Västra Götalandsregionen
    • GÖTEBORG
    • Accreditation
    • Molecular diagnosis of FGFR/TWIST-related craniosynostoses (FGFR1, FGFR2, FGFR3 and TWIST1 genes)
    • Sahlgrenska university hospital
    • More information
    • SPAIN
    • Cataluña
    • L'HOSPITALET DE LLOBREGAT
    • Accreditation
    • Molecular diagnosis of Carpenter syndrome (RAB23 gene)
    • Reference Laboratory Genetics
    • More information
    • SPAIN
    • Cataluña
    • L'HOSPITALET DE LLOBREGAT
    • Accreditation
    • Molecular diagnosis of craniosynostosis (FGFR1, FGFR2, FGFR3, MSX2, TWIST1, GLI3 genes)
    • Reference Laboratory Genetics
    • More information
    • FRANCE
    • BRETAGNE
    • BREST
    • Molecular diagnosis of dysmorphological syndromes by CGH array
    • CHRU de Brest - Hôpital Morvan
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of Carpenter disease (RAB23 gene sequencing)
    • CHU Paris-GH St-Louis Lariboisière F-Widal - Hôpital Lariboisière
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Molecular diagnosis of craniosynostosis (MLPA and sequencing of FGFR2, FGFR3, TWIST1, MSX2, TCF12, ERF genes)
    • CHU Paris-GH St-Louis Lariboisière F-Widal - Hôpital Lariboisière
    • More information
    • SPAIN
    • Aragón
    • ZARAGOZA
    • Molecular diagnostic of syndromic craniosynostosis (FGFR2, FGFR3, TWIST1 genes)
    • Universidad de Zaragoza. Facultad de Medicina
    • More information
    • SPAIN
    • Madrid
    • MADRID
    • Molecular diagnosis of craniosynostosis syndrome or cranial ossification disease (FGFR1, FGFR2, FGFR3, TWIST1, MSX2, ALX4, EFNB1 genes)
    • Fundación Jiménez Díaz
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Molecular diagnosis of Craniosynostosis (FGFR1, FGFR2, and FGFR3 genes)
    • Praxis für Humangenetik
    • More information
    • GREECE
    • ATTIKI
    • ATHENS
    • Molecular diagnosis of non-syndromic and syndromic craniosynostosis (FGFR1, FGFR2,FGFR3, TWIST, EFNB1 genes: sequencing, MLPA, a-CGH)
    • Leto Maternity Hospital
    • More information
    • SPAIN
    • Comunidad Valenciana
    • SANT JOAN D'ALACANT
    • Molecular diagnosis of craniosynostosis (FGFR1, FGFR2, FGFR3 genes / sequencing)
    • Centro Inmunológico de Alicante (CIALAB)
    • More information
    • ITALY
    • EMILIA ROMAGNA
    • BOLOGNA
    • Molecular diagnosis of craniosynostosis (FGFR1, FGFR2, FGFR3, TWIST genes)
    • Policlinico S. Orsola-Malpighi - Area S. Orsola
    • More information
    • SPAIN
    • Comunidad Valenciana
    • VALENCIA
    • Molecular diagnosis of craniosynostosis (sequentiation of TWIST1, FGFR2 and/or FGFR3 genes)
    • INCLIVA
    • More information