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Nonsyndromic craniosynostosis: novel coding variants.
Sewda, Anshuman; White, Sierra R; Erazo, Monica; Hao, Ke; García-Fructuoso, Gemma; Fernández-Rodriguez, Ivette; Heuzé, Yann; Richtsmeier, Joan T; Romitti, Paul A; Reva, Boris; Jabs, Ethylin Wang; Peter, Inga.
Afiliação
  • Sewda A; Department of Genetics & Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA. anshuman.sewda@mssm.edu.
  • White SR; Department of Genetics & Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Erazo M; Department of Genetics & Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Hao K; Department of Genetics & Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • García-Fructuoso G; Department of Pediatric Neurosurgery, Hospital Sant Joan de Déu, Barcelona, Spain.
  • Fernández-Rodriguez I; Department of Pediatric Neurosurgery, Hospital Sant Joan de Déu, Barcelona, Spain.
  • Heuzé Y; University Bordeaux, CNRS, MCC, PACEA, UMR5199, Bordeaux Archaeological Sciences Cluster of Excellence, Pessac, France.
  • Richtsmeier JT; Department of Anthropology, Pennsylvania State University, University Park, PA, USA.
  • Romitti PA; Department of Epidemiology, College of Public Health, University of Iowa, Iowa City, IA, USA.
  • Reva B; Department of Genetics & Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Jabs EW; Department of Genetics & Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
  • Peter I; Department of Genetics & Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Pediatr Res ; 85(4): 463-468, 2019 03.
Article em En | MEDLINE | ID: mdl-30651579

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Craniossinostoses Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Craniossinostoses Idioma: En Ano de publicação: 2019 Tipo de documento: Article