17 Result(s)

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• • FRANCE
  • AQUITAINE
  • BORDEAUX
  • Phenotypic characterisation and search for chromosomic reorganisation in patients with not identified syndromic obesity
  • CHU de Bordeaux - Hôpital Pellegrin
  • Service de génétique médicale
  • More details
• • FRANCE
  • BASSE NORMANDIE
  • CAEN
  • Genetic lesions of the GS alpha protein (GNAS1) in Albright osteodystrophy and pseudohypoparathyroïdism type 1A and 1B
  • CHU Hôpital Clémenceau
  • Laboratoire de génétique moléculaire
  • More details
• • FRANCE
  • BASSE NORMANDIE
  • CAEN
  • Genetic lesions on GNAS1 locus and genetic parental errors
  • Université de Caen
  • Laboratoire estrogènes et reproduction
  • More details
• • FRANCE
  • ILE DE FRANCE
  • PARIS
  • Genetics of inherited osteochondrodysplasias and disorders of calcium and phosphate metabolism
  • GHU Cochin - Saint-Vincent de Paul / Site Saint-Vincent de Paul
  • Immunologie, génétique et traitement des maladies métaboliques et du diabète
  • More details
• • FRANCE
  • ILE DE FRANCE
  • PARIS
  • Study of mechanism of obesity and osseus anomalies of pseudohypoparathyroidisms
  • GHU Cochin - Saint-Vincent de Paul / Site Saint-Vincent de Paul
  • Immunologie, génétique et traitement des maladies métaboliques et du diabète
  • More details
• • GERMANY
  • Baden-Württemberg
  • FREIBURG
  • Molecular background of skeletal dysplasias
  • Universitätsklinikum Freiburg
  • Klinik I - Allgemeine Kinderheilkunde, Neonatologie und Jugendmedizin
  • More details
• • GERMANY
  • Bayern
  • ERLANGEN
  • SKELNET : Characterization of candidate genes for skeletal dysplasias
  • Friedrich-Alexander-Universität Erlangen-Nürnberg
  • Humangenetisches Institut
  • More details
• • GERMANY
  • Bayern
  • ERLANGEN
  • SKELNET : Analysis of genotype phenotype correlation in skeletal dysplasias by cell culture systems and recombinant protein technology
  • Medizinische Fakultät der Universität Erlangen-Nürnberg
  • Experimentelle Medizin I
  • More details
• • GERMANY
  • Bremen
  • BREMEN
  • SKELNET : A cooperative approach from patient organisations and experts for better understanding and care of skeletal dysplasias
  • Bundesverband Kleinwüchsige Menschen und ihre Familien e.V.
  • More details
• • GERMANY
  • Nordrhein-Westfalen
  • ESSEN
  • SKELNET : Chondrocyte specific genes as part of the signaling regulation of chondrocyte differentiation
  • Universität Duisburg-Essen
  • Abteilung Entwicklungsbiologie
  • More details
• • GERMANY
  • Sachsen
  • LEIPZIG
  • NGFN NeuroNet: Population genetics and molecular evolution of candidate genes for obesity
  • Max-Planck-Institut für evolutionäre Anthropologie
  • Department of Evolutionary Genetics
  • More details
• • GERMANY
  • Sachsen
  • WEIßWASSER
  • GNAS1 gene : Duplication/deletion analysis
  • Praxis Dr. Mato Nagel
  • Molekulargenetisches Labor
  • More details
• • GERMANY
  • Schleswig-Holstein
  • LÜBECK
  • SKELNET : Albright hereditary osteodystrophy : Clinical, functional and molecular changes
  • Universitätsklinikum Schleswig-Holstein, Campus Lübeck
  • Sektion für Pädiatrische Endokrinologie und Diabetologieie
  • More details
• • SPAIN
  • Andalucía
  • BARAKALDO
  • Genetic and molecular analysis of primary hypoparathyroidism (PTH and CaSR genes) and pseudohypoparathyroidism (Gs protein)
  • Hospital de Cruces - Osakidetza
  • Unidad de Investigación. Laboratorio de Genética Molecular
  • More details
• • UNITED KINGDOM
  • Greater London
  • LONDON
  • Natural history and management in Skeletal Dysplasias
  • Great Ormond Street Hospital for Children
  • NE Thames Regional Genetics Service
  • More details
• • UNITED KINGDOM
  • Greater London
  • LONDON
  • Natural history and management in Albright Osteodystrophy
  • Great Ormond Street Hospital for Children
  • NE Thames Regional Genetics Service
  • More details
• • UNITED KINGDOM
  • Greater London
  • LONDON
  • Early-onset syndromal and non-syndromal obesity: gaining a greater understanding of the genetics and biology of rare disorders in order to apply the more common biochemical pathways to the more complex disorders
  • UCL Institute of Child Health
  • Molecular Medicine Unit
  • More details