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A Genome-Wide Pharmacogenetic Study of Growth Hormone Responsiveness.
Dauber, Andrew; Meng, Yan; Audi, Laura; Vedantam, Sailaja; Weaver, Benjamin; Carrascosa, Antonio; Albertsson-Wikland, Kerstin; Ranke, Michael B; Jorge, Alexander A L; Cara, Jose; Wajnrajch, Michael P; Lindberg, Anders; Camacho-Hübner, Cecilia; Hirschhorn, Joel N.
Affiliation
  • Dauber A; Division of Endocrinology, Children's National Hospital, Washington, DC.
  • Meng Y; Division of Endocrinology, Boston Children's Hospital, and Program in Medical and Population Genetics, Broad Institute, Harvard Medical School, Boston, Massachusetts.
  • Audi L; Department of Pediatrics, Institut de Recerca (VHIR), Hospital Vall d'Hebron, Centre for Biomedical Research on Rare Diseases (CIBERER), Autonomous University, Barcelona, Spain.
  • Vedantam S; Division of Endocrinology, Boston Children's Hospital, and Program in Medical and Population Genetics, Broad Institute, Harvard Medical School, Boston, Massachusetts.
  • Weaver B; Division of Endocrinology, Boston Children's Hospital, and Program in Medical and Population Genetics, Broad Institute, Harvard Medical School, Boston, Massachusetts.
  • Carrascosa A; Department of Pediatrics, Institut de Recerca (VHIR), Hospital Vall d'Hebron, Centre for Biomedical Research on Rare Diseases (CIBERER), Autonomous University, Barcelona, Spain.
  • Albertsson-Wikland K; Department of Physiology/Endocrinology, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Ranke MB; University Children´s Hospital, Paediatric Endocrinology, Tübingen, Germany.
  • Jorge AAL; Unidade de Endocrinologia do Desenvolvimento (LIM42), Hospital das Clinicas da Faculdade de Medicina da Universidade de Sao Paulo, Sao Paulo, Brazil.
  • Cara J; Pfizer Inc, Rare Disease, New York.
  • Wajnrajch MP; Pfizer Inc, Rare Disease, New York.
  • Lindberg A; Pfizer, Data Management, Sollentuna, Sweden.
  • Camacho-Hübner C; Pfizer Inc, Rare Disease, New York.
  • Hirschhorn JN; Division of Endocrinology, Boston Children's Hospital, and Program in Medical and Population Genetics, Broad Institute, Harvard Medical School, Boston, Massachusetts.
J Clin Endocrinol Metab ; 105(10)2020 10 01.
Article de En | MEDLINE | ID: mdl-32652002
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Taille / Hormone de croissance humaine / Nanisme hypophysaire / Locus génétiques Type d'étude: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Child / Female / Humans / Male Langue: En Journal: J Clin Endocrinol Metab Année: 2020 Type de document: Article Pays de publication: États-Unis d'Amérique
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Taille / Hormone de croissance humaine / Nanisme hypophysaire / Locus génétiques Type d'étude: Clinical_trials / Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limites: Child / Female / Humans / Male Langue: En Journal: J Clin Endocrinol Metab Année: 2020 Type de document: Article Pays de publication: États-Unis d'Amérique