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Bone health and SATB2-associated syndrome.
Zarate, Y A; Steinraths, M; Matthews, A; Smith, W E; Sun, A; Wilson, L C; Brain, C; Allgove, J; Jacobs, B; Fish, J L; Powell, C M; Wasserman, W W; van Karnebeek, C D; Wakeling, E L; Ma, N S.
Afiliação
  • Zarate YA; Section of Genetics and Metabolism, University of Arkansas for Medical Sciences, Little Rock, Arkansas.
  • Steinraths M; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
  • Matthews A; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
  • Smith WE; Centre for Molecular Medicine and Therapeutics, British Columbia Children's Hospital Research Institute, Vancouver, Canada.
  • Sun A; Department of Pediatrics, The Barbara Bush Children's Hospital, Maine Medical Center, Portland, Maine.
  • Wilson LC; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, Washington.
  • Brain C; Department of Genetics, Great Ormond Street for Children NHS Foundation Trust, London, UK.
  • Allgove J; Department of Endocrinology, Great Ormond Street for Children NHS Foundation Trust, London, UK.
  • Jacobs B; Department of Endocrinology, Great Ormond Street for Children NHS Foundation Trust, London, UK.
  • Fish JL; Department of Pediatrics, Royal National Orthopaedic Hospital NHS Trust, London, UK.
  • Powell CM; Department of Biological Sciences, University of Massachusetts Lowell, Lowell, Massachusetts.
  • Wasserman WW; Department of Pediatrics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • van Karnebeek CD; Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Wakeling EL; Department of Medical Genetics, University of British Columbia, Vancouver, Canada.
  • Ma NS; Centre for Molecular Medicine and Therapeutics, British Columbia Children's Hospital Research Institute, Vancouver, Canada.
Clin Genet ; 93(3): 588-594, 2018 03.
Article em En | MEDLINE | ID: mdl-28787087
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Desenvolvimento Ósseo / Doenças do Desenvolvimento Ósseo / Predisposição Genética para Doença / Proteínas de Ligação à Região de Interação com a Matriz / Estudos de Associação Genética Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article
Texto completo
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fatores de Transcrição / Desenvolvimento Ósseo / Doenças do Desenvolvimento Ósseo / Predisposição Genética para Doença / Proteínas de Ligação à Região de Interação com a Matriz / Estudos de Associação Genética Tipo de estudo: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2018 Tipo de documento: Article