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Caption : Accreditation =Accreditation
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    • GERMANY
    • Bayern
    • MÜNCHEN
    • Accreditation
    • Molecular diagnosis of creatine transporter deficiency (SLC6A8 gene)
    • Medizinisch Genetisches Zentrum München
    • More information
    • SWITZERLAND
    • Suisse Alémanique
    • SCHLIEREN
    • Accreditation
    • Search of genomic DNA duplications and/or deletions by CGH arrays
    • Universität Zürich
    • More information
    • GERMANY
    • Sachsen
    • DRESDEN
    • Accreditation
    • Molecular diagnosis of creatine transporter deficiency (SLC6A8 gene: sequencing)
    • Gemeinschaftspraxis Dr. Prager / Dr. Junge / Dr. Hennig / Dr. Linné
    • More information
    • GERMANY
    • Baden-Württemberg
    • MANNHEIM
    • Accreditation
    • Molecular diagnosis of creatine transporter deficiency (SLC6A8 gene)
    • Zentrum für Humangenetik Mannheim
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Multiple Congenital Anomalies (SNP-array)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Unexplained Intellectual Deficit with Multiple Congenital Anomalies (SNP-array)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis in case of Unexplained Metabolic Disorders (exome sequencing)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • NETHERLANDS
    • Gelderland
    • NIJMEGEN
    • Accreditation
    • Molecular diagnosis of X-linked Intellectual Deficit due to X-chromosome Inactivation (RFLP and methylation analysis of x-chromosome)
    • Radboudumc - Radboud universitair medisch centrum
    • More information
    • GERMANY
    • Baden-Württemberg
    • FREIBURG
    • Accreditation
    • Molecular diagnosis of creatine transporter deficiency (SLC6A8 gene)
    • Praxis für Humangenetik Freiburg
    • More information
    • GERMANY
    • Mecklenburg-Vorpommern
    • ROSTOCK
    • Accreditation
    • Molecular diagnosis of creatine transporter deficiency (SLC6A8 gene)
    • Centogene AG
    • More information
    • NETHERLANDS
    • Utrecht
    • UTRECHT
    • Accreditation
    • Biochemical diagnosis of Creatine Synthesis Defects (Analyte: Creatine and Guanidinoacetate in urine and plasma)
    • UMC Utrecht - Universitair Medisch Centrum Utrecht
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Molecular diagnosis of Creatine Transporter Deficiency (SLC6A8 gene)
    • VUmc - VU medisch centrum
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Biochemical diagnosis of Creatine Transporter Deficiency (Analyte: Creatine Transporter)
    • VUmc - VU medisch centrum
    • More information
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • Accreditation
    • Biochemical diagnosis of X-linked creatine transporter deficiency (Analyte: urine and plasma creatine and guanidinoacetate)
    • Addenbrooke's Hospital
    • More information
    • UNITED KINGDOM
    • Cambridgeshire
    • CAMBRIDGE
    • Accreditation
    • Biochemical diagnosis of creatine bisosynthesis disorder (Analyte: urine and plasma creatine and guanidinoacetate)
    • Addenbrooke's Hospital
    • More information
    • NETHERLANDS
    • Noord-Holland
    • AMSTERDAM
    • Accreditation
    • Biochemical diagnosis of Creatine Synthesis and Transport Disorders (Analyte: Creatine and Guanidinoacetic Acid)
    • AMC - Academisch Medisch Centrum
    • More information
    • FRANCE
    • RHONE-ALPES
    • BRON
    • Biochemical and molecular diagnosis of creatine transporter deficiency (SLC6A8 gene)
    • CHU de Lyon HCL - GH Est
    • More information
    • FRANCE
    • NORD-PAS-DE-CALAIS
    • LILLE
    • Biochemical diagnosis of creatine transporter deficiency
    • CHRU de Lille - Centre de biologie pathologie génétique
    • More information
    • ITALY
    • LAZIO
    • ROMA
    • Molecular and biochemical diagnosis of creatine transporter deficiency (SLC6A8 gene)
    • Policlinico Umberto I
    • More information
    • SPAIN
    • País Vasco
    • SAN SEBASTIÁN
    • Molecular diagnosis of X-linked intellectual deficit syndromes (MLPA kit P106B1)
    • Policlínica Gipuzkoa
    • More information
    • SPAIN
    • Baleares
    • PALMA DE MALLORCA
    • Molecular diagnosis of X-linked intellectual deficit (RPS6KA3, ARX, IL1RAPL1, TSPAN7, PQBP1, HUWE1, OPHN1, ACSL4, PAK3, DCX, AGTR2, ARHGEF6, FMR1, AFF2, SLC6A8 and GDI1 genes by MLPA (kit P106))
    • Hospital Universitario Son Espases
    • More information
    • SPAIN
    • Madrid
    • CANTOBLANCO
    • Biochemical and molecular diagnosis of X-linked creatine transporter deficiency (SLC6A8 gene)
    • Universidad Autónoma de Madrid. Facultad de Ciencias
    • More information
    • ITALY
    • VENETO
    • PADOVA
    • Biochemical diagnosis of creatine biosynthesis disorder
    • Azienda Ospedaliera Universitaria di Padova - Campus Biomedico Pietro d'Abano
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Molecular diagnosis of creatine transporter deficiency (SLC6A8 gene)
    • Centre Hospitalier Universitaire Vaudois CHUV
    • More information
    • BELGIUM
    • LIEGE
    • LIEGE
    • Biochemical diagnosis of Creatine Disorders (Creatine and Guanidionoacetate by GCMSMS: urine)
    • CHU Sart Tilman - Liège
    • More information
    • CANADA
    • Québec
    • SHERBROOKE
    • Biochemical analysis of creatine and guanidinoacetate in urine by LC/MS
    • CHU Sherbrooke - Hôpital Fleurimont
    • More information
    • SPAIN
    • La Rioja
    • LOGROÑO
    • Molecular diagnosis of X-linked creatine transporter deficiency (SLC6A8 gene)
    • CIBIR - Centro de Investigación Biomédica de La Rioja
    • More information
    • SPAIN
    • Cataluña
    • BARCELONA
    • Cerebral Creatine Transporter Deficiency Biochemical Diagnosis
    • Hospital Clínic de Barcelona
    • More information
    • GERMANY
    • Bayern
    • NÜRNBERG
    • Molecular diagnosis of creatine transporter deficiency (SLC6A8 gene)
    • Medizinisches Versorgungszentrum
    • More information
    • PORTUGAL
    • NORTE
    • PORTO
    • Biochemical diagnosis of creatine transporter deficiency
    • CGMJM - Centro de Genética Médica Jacinto Magalhães
    • More information
    • FRANCE
    • ILE-DE-FRANCE
    • PARIS
    • Biochemical diagnosis of mental retardations, X linked, with seizures, short stature, and midface hypoplasia
    • CHU Paris - Hôpital Necker-Enfants Malades
    • More information
    • SWITZERLAND
    • Suisse Romande
    • LAUSANNE
    • Screen of Creatine / Guanidinoacetate in plasma, urine, liquor
    • Centre Hospitalier Universitaire Vaudois CHUV
    • More information
    • SPAIN
    • País Vasco
    • BARAKALDO
    • Biochemical diagnosis of disorders related to creatine biosynthesis
    • Hospital Universitario Cruces - Osakidetza
    • More information
    • GERMANY
    • Baden-Württemberg
    • HEIDELBERG
    • Biochemical diagnosis of kreatine synthese defects (guanidino compounds -creatine, creatinine, guanidino acetate- in urine/plasma/CSF)
    • Dietmar-Hopp-Stoffwechselzentrum
    • More information
    • GERMANY
    • Niedersachsen
    • GÖTTINGEN
    • Biochemical diagnosis of kreatine synthese defects (guanidino acetate, creatine, creatine/creatinine quotient - in urine/plasma/CSF)
    • Universitätsmedizin Göttingen
    • More information
    • SPAIN
    • Cataluña
    • ESPLUGUES DE LLOBREGAT
    • Biochemical diagnosis of X-linked creatine transporter deficiency (analyte: Urine guanidinoacetate and creatine/creatinine ratio)
    • Hospital Universitari Sant Joan de Déu
    • More information
    • POLAND
    • Warszawa
    • WARSAW
    • Molecular diagnosis of X-linked intellectual deficit syndromes (MLPA kit P106)
    • The Children's Memorial Health Institute CMHI (IP-CZD)
    • More information
    • AUSTRIA
    • WIEN
    • WIEN
    • Biochemical diagnosis of inborn errors of metabolism (including Austrian newborn screening program for inborn errors of metabolism)
    • Medizinische Universität Wien
    • More information