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29 Resultaat/Resultaten
Titel
: Accreditatie
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DUITSLAND
Bayern
MARTINSRIED
Molecular diagnosis of osteogenesis imperfecta (NGS screening panel, 14 genes)
Zentrum für Humangenetik und Laboratoriumsdiagnostik (MVZ)
ZWITSERLAND
Suisse Romande
GENÈVE
Search of duplications and/or deletions by array-CGH
Hôpitaux Universitaires de Genève HUG
DUITSLAND
Baden-Württemberg
FREIBURG
Molecular diagnosis of Bruck syndrome (PLOD2 gene)
Synlab MVZ Freiburg GmbH
BELGIË
OOST-VLAANDEREN
GENT
Molecular diagnosis of Osteogenesis Imperfecta, autosomal recessive (BMP1, CREB3L1, CRTAP, FKBP10, LEPRE1, PPIB, SERPINF1, SERPINH1, SP7, TMEM38B, WNT1, P4HB, B6GALT6, TAPT1 genes)
Center for Medical Genetics Gent
VERENIGD KONINKRIJK
South Yorkshire
SHEFFIELD
Molecular diagnosis of Bruck Syndrome (PLOD2 and FKBP10: sequencing of coding regions)
Sheffield Children's NHS Foundation Trust
DUITSLAND
Rheinland-Pfalz
INGELHEIM AM RHEIN
Molecular diagnosis of Bruck syndrome (PLOD2 gene)
Bioscientia Institut für Medizinische Diagnostik GmbH
DUITSLAND
Baden-Württemberg
FREIBURG
Molecular diagnosis of Bruck syndrome (FKBP10 gene)
Synlab MVZ Freiburg GmbH
CANADA
Ontario
TORONTO
Molecular Diagnosis of Connective Tissue Disorder: Osteogenesis Imperfecta NGS Panel (20 genes)
The Hospital for Sick Children and University of Toronto
SPANJE
Cataluña
L'HOSPITALET DE LLOBREGAT
Diagnosis of osteogenesis imperfecta (gene panel)
Reference Laboratory Genetics
BELGIË
OOST-VLAANDEREN
GENT
Molecular diagnosis of Bruck Syndrome (FKBP10, PLOD2 genes)
Center for Medical Genetics Gent
FRANKRIJK
ILE-DE-FRANCE
PARIS
Diagnosis of osteogenesis imperfecta (Panel)
CHU Paris - Hôpital Necker-Enfants Malades
NEDERLAND
Noord-Holland
AMSTERDAM
Molecular diagnosis of Osteogenesis Imperfecta and Related Disorders (gene panel)
Amsterdam UMC, locatie VUmc
SPANJE
Cataluña
L'HOSPITALET DE LLOBREGAT
Diagnosis of Bruck syndrome (gene panel)
Reference Laboratory Genetics
DUITSLAND
Bayern
MÜNCHEN
Molecular diagnosis of mental retardation and dysmorphology (NGS screening panel, 353 genes)
Medizinisch Genetisches Zentrum München
ZWITSERLAND
Suisse Romande
LAUSANNE
Molecular diagnosis of osteogenesis imperfecta (PLOD2 gene); complete sequencing
Centre Hospitalier Universitaire Vaudois CHUV
DUITSLAND
Niedersachsen
OSNABRÜCK
Molecular diagnosis of Bruck syndrome (PLOD2 gene: sequencing of exon 2)
Praxis Dres. Gencik
DUITSLAND
Nordrhein-Westfalen
KÖLN
Molecular diagnosis of osteogenesis imperfecta and osteoporosis (NGS panel, 23 genes)
Institut für Humangenetik am Universitätsklinikum Köln
SPANJE
Comunidad Valenciana
PATERNA
Molecular diagnosis of Bruck syndrome (PLOD2 gene)
Sistemas Genómicos S.L.
SPANJE
Comunidad Valenciana
SANT JOAN D'ALACANT
Molecular diagnosis of Bruck syndrome (PLOD2 gene / entire coding sequence)
Centro Inmunológico de Alicante (CIALAB)
DUITSLAND
Nordrhein-Westfalen
KÖLN
Molecular diagnosis of Bruck syndrome (FKBP10, PLOD2 genes)
Institut für Humangenetik am Universitätsklinikum Köln
PORTUGAL
NORTE
PORTO
Molecular diagnosis of Bruck syndrome (PLOD2 gene: sequencing of the entire conding region)
CGC Genetics / Centro de Genética Clínica
SPANJE
Comunidad Valenciana
PATERNA
Molecular diagnosis of Bruck syndrome (PLOD2 gene)
IMEGEN - Instituto de Medicina Genómica
DUITSLAND
Nordrhein-Westfalen
DÜSSELDORF
Array-CGH in case of unexplained developmental delay
Praenatal-Medizin und Genetik, Düsseldorf
SPANJE
Madrid
SAN SEBASTIÁN DE LOS REYES