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Tibial hemimelia associated with GLI3 truncation.
Deimling, Steven; Sotiropoulos, Chris; Lau, Kimberly; Chaudhry, Sonia; Sturgeon, Kendra; Kelley, Simon; Narayanan, Unni; Howard, Andrew; Hui, Chi-Chung; Hopyan, Sevan.
Afiliação
  • Deimling S; Program in Developmental and Stem Cell Biology, Research Institute, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Sotiropoulos C; Program in Developmental and Stem Cell Biology, Research Institute, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Lau K; Program in Developmental and Stem Cell Biology, Research Institute, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Chaudhry S; Division of Orthopaedic Surgery, The Hospital for Sick Children and University of Toronto, Toronto, Ontario, Canada.
  • Sturgeon K; Program in Developmental and Stem Cell Biology, Research Institute, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Kelley S; Division of Orthopaedic Surgery, The Hospital for Sick Children and University of Toronto, Toronto, Ontario, Canada.
  • Narayanan U; Division of Orthopaedic Surgery, The Hospital for Sick Children and University of Toronto, Toronto, Ontario, Canada.
  • Howard A; Division of Orthopaedic Surgery, The Hospital for Sick Children and University of Toronto, Toronto, Ontario, Canada.
  • Hui CC; Program in Developmental and Stem Cell Biology, Research Institute, The Hospital for Sick Children, Toronto, Ontario, Canada.
  • Hopyan S; Department of Molecular Genetics, University of Toronto, Toronto, Ontario, Canada.
J Hum Genet ; 61(5): 443-6, 2016 May.
Article em En | MEDLINE | ID: mdl-26791356
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Tíbia / Ectromelia / Fatores de Transcrição Kruppel-Like / Mutação / Proteínas do Tecido Nervoso Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: J Hum Genet Ano de publicação: 2016 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fenótipo / Tíbia / Ectromelia / Fatores de Transcrição Kruppel-Like / Mutação / Proteínas do Tecido Nervoso Tipo de estudo: Prognostic_studies / Risk_factors_studies Limite: Animals / Humans Idioma: En Revista: J Hum Genet Ano de publicação: 2016 Tipo de documento: Article