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CLARITY: Co-occurrences in achondroplasia-craniosynostosis, seizures, and decreased risk of diabetes mellitus.
Legare, Janet M; Pauli, Richard M; Hecht, Jacqueline T; Bober, Michael B; Smid, Cory J; Modaff, Peggy; Little, Mary Ellen; Rodriguez-Buritica, David F; Serna, Maria Elena; Alade, Adekemi Yewande; Liu, Chengxin; Hoover-Fong, Julie E; Hashmi, S Shahrukh.
Afiliação
  • Legare JM; Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
  • Pauli RM; Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
  • Hecht JT; Department of Pediatrics, McGovern Medical School at UT Health, Houston, Texas, USA.
  • Bober MB; Department of Pediatrics, A. l. duPont Hospital for Children, Thomas Jefferson University, Wilmington, Delaware, USA.
  • Smid CJ; Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
  • Modaff P; Department of Genetics, Children's Wisconsin; Medical College of Wisconsin, Milwaukee, Wisconsin, USA.
  • Little ME; Department of Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin, USA.
  • Rodriguez-Buritica DF; Department of Pediatrics, A. l. duPont Hospital for Children, Thomas Jefferson University, Wilmington, Delaware, USA.
  • Serna ME; Department of Pediatrics, McGovern Medical School at UT Health, Houston, Texas, USA.
  • Alade AY; Department of Pediatrics, McGovern Medical School at UT Health, Houston, Texas, USA.
  • Liu C; Department of Epidemiology, Johns Hopkins University, Baltimore, Maryland, USA.
  • Hoover-Fong JE; Greenberg Center for Skeletal Dysplasias, McKusick Nathans Department of Genetic Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
  • Hashmi SS; Greenberg Center for Skeletal Dysplasias, McKusick Nathans Department of Genetic Medicine, Johns Hopkins University, Baltimore, Maryland, USA.
Am J Med Genet A ; 185(4): 1168-1174, 2021 04.
Article em En | MEDLINE | ID: mdl-33496070
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteocondrodisplasias / Convulsões / Acondroplasia / Craniossinostoses Tipo de estudo: Diagnostic_studies / Etiology_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Osteocondrodisplasias / Convulsões / Acondroplasia / Craniossinostoses Tipo de estudo: Diagnostic_studies / Etiology_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Am J Med Genet A Assunto da revista: GENETICA MEDICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Estados Unidos País de publicação: Estados Unidos