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Rare EN1 Variants and Pediatric Bone Mass.
Mitchell, Jonathan A; Chesi, Alessandra; McCormack, Shana E; Roy, Sani M; Cousminer, Diana L; Kalkwarf, Heidi J; Lappe, Joan M; Gilsanz, Vicente; Oberfield, Sharon E; Shepherd, John A; Kelly, Andrea; Zemel, Babette S; Grant, Struan Fa.
Afiliación
  • Mitchell JA; Division of Gastroenterology, Hepatology, and Nutrition, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Chesi A; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • McCormack SE; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Roy SM; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Cousminer DL; Division of Endocrinology and Diabetes, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Kalkwarf HJ; Division of Endocrinology and Diabetes, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Lappe JM; Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA, USA.
  • Gilsanz V; Division of Gastroenterology, Hepatology, and Nutrition, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, USA.
  • Oberfield SE; Division of Endocrinology, Department of Medicine, Creighton University, Omaha, NE, USA.
  • Shepherd JA; Department of Radiology, Children's Hospital Los Angeles, Los Angeles, CA, USA.
  • Kelly A; Division of Pediatric Endocrinology, Diabetes, and Metabolism, Department of Pediatrics, Columbia University Medical Center, New York, NY, USA.
  • Zemel BS; Department of Radiology, University of California San Francisco, San Francisco, CA, USA.
  • Grant SF; Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
J Bone Miner Res ; 31(8): 1513-7, 2016 08.
Article en En | MEDLINE | ID: mdl-26970088
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Huesos / Sitios Genéticos Tipo de estudio: Prognostic_studies Límite: Child / Female / Humans / Male Idioma: En Revista: J Bone Miner Res Asunto de la revista: METABOLISMO / ORTOPEDIA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Huesos / Sitios Genéticos Tipo de estudio: Prognostic_studies Límite: Child / Female / Humans / Male Idioma: En Revista: J Bone Miner Res Asunto de la revista: METABOLISMO / ORTOPEDIA Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos