20 Result(s)

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• • GERMANY
  • Sachsen
  • WEIßWASSER
  • 
  • Molecular diagnosis of Albright hereditary osteodystrophy (GNAS gene)
  • Praxis Dr. Mato Nagel
  • More information
• • GERMANY
  • Sachsen
  • WEIßWASSER
  • 
  • Molecular diagnosis of pseudohypoparathyroidism type 1B, C (GNAS and STX16 genes)
  • Praxis Dr. Mato Nagel
  • More information
• • NETHERLANDS
  • Utrecht
  • UTRECHT
  • 
  • Molecular diagnosis of Albright Hereditary Osteodystrophy (GNAS gene)
  • UMC Utrecht - Universitair Medisch Centrum Utrecht
  • More information
• • UNITED KINGDOM
  • Greater London
  • LONDON
  • 
  • Molecular diagnosis of Albright Hereditary Osteodystrophy (GNAS1 gene mutation disorders)
  • Great Ormond Street Hospital for Children
  • More information
• • FRANCE
  • BASSE NORMANDIE
  • CAEN
  • 
  • Molecular diagnosis of Albright hereditary osteodystrophy : search for mutations in GNAS gene and microdeletion in STX16 gene
  • CHU Hôpital Clémenceau
  • More information
• • ITALY
  • LOMBARDIA
  • MILANO
  • 
  • Molecular cytogenetic diagnosis of Albright hereditary osteodystrophy
  • Istituto Auxologico Italiano
  • More information
• • BELGIUM
  • ARRONDISSEMENT BRUSSEL HOOFDSTAD
  • BRUXELLES
  • Molecular diagnosis of Albright hereditary osteodystrophy (GNAS gene)
  • Hôpital Erasme
  • More information
• • GERMANY
  • Niedersachsen
  • OSNABRÜCK
  • Molecular diagnosis of pseudohypoparathyroidism type Ia (GNAS gene)
  • Zentrum für medizinische Genetik Osnabrück
  • More information
• • SPAIN
  • Andalucía
  • BARAKALDO
  • Molecular Diagnosis of Pseudohypoparathyroidism 1A, 1B and Albright hereditary osteodystrophy. Gene GNAS.
  • Hospital de Cruces - Osakidetza
  • More information
• • FRANCE
  • HAUTE NORMANDIE
  • ROUEN
  • Biochemical diagnosis of pseudohypoparathyroidism
  • CRLCC - Henri Becquerel
  • More information
• • FRANCE
  • ILE DE FRANCE
  • PARIS
  • Diagnosis of albright hereditary osteodystrophy by exploration of the renal function
  • CHU Hôpital Européen Georges Pompidou
  • More information
• • FRANCE
  • ILE DE FRANCE
  • PARIS
  • Molecular diagnosis of Albright hereditary osteodystrophy (GNAS1 gene)
  • CHU Hôpital Xavier Bichat - Claude Bernard
  • More information
• • FRANCE
  • ILE DE FRANCE
  • PARIS
  • Molecular cytogenetic diagnosis of Albright hereditary osteodystrophy (FISH analysis of 20q13.3 deletion - GNAS gene)
  • Hopital Necker - Enfants Malades
  • More information
• • FRANCE
  • ILE DE FRANCE
  • POISSY
  • Molecular diagnosis of Albright hereditary osteodystrophy
  • Centre hospitalier intercommunal Poissy-Saint-Germain-en-Laye
  • More information
• • FRANCE
  • PAYS DE LOIRE
  • ANGERS
  • Molecular diagnosis of hypothyroidism and familial hyperthyroidism due to mutations in TSH receptor or GSalpha subunit (TSHR and GNAS genes)
  • CHU d'Angers
  • More information
• • FRANCE
  • PROVENCE-ALPES-COTE D'AZUR
  • MARSEILLE
  • Molecular diagnosis of pseudohypoparathyroidism type Ia and Ib (GNAS gene)
  • Hôpital de la Conception - AP-HM
  • More information
• • GERMANY
  • Schleswig-Holstein
  • LÜBECK
  • Biochemical diagnosis of Albright hereditary osteodystrophy
  • Universitätsklinikum Schleswig-Holstein, Campus Lübeck
  • More information
• • ITALY
  • LOMBARDIA
  • MILANO
  • Molecular diagnosis of Albright hereditary osteodystrophy
  • Fondazione IRCCS Ospedale Maggiore Policlinico Mangiagalli e Regina Elena
  • More information
• • NETHERLANDS
  • Noord-Holland
  • AMSTERDAM
  • Molecular diagnosis of Albright hereditary osteodystrophy (GNAS gene)
  • Academic Medical Center / University of Amsterdam
  • More information
• • UNITED KINGDOM
  • Wiltshire
  • SALISBURY
  • Molecular Cytogenetic diagnosis of Albright hereditary osteodystrophy (by FISH of JAG1)
  • Salisbury District Hospital
  • More information