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Causal somatic mutations in urine DNA from persons with the CLOVES subgroup of the PIK3CA-related overgrowth spectrum.
Michel, M E; Konczyk, D J; Yeung, K S; Murillo, R; Vivero, M P; Hall, A M; Zurakowski, D; Adams, D; Gupta, A; Huang, A Y; Chung, B H Y; Warman, M L.
Afiliação
  • Michel ME; Department of Orthopaedic Surgery, Orthopaedic Research Laboratories, Boston Children's Hospital, Boston, Massachusetts.
  • Konczyk DJ; Department of Plastic and Oral Surgery, Boston Children's Hospital, Boston, Massachusetts.
  • Yeung KS; Department of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
  • Murillo R; Department of Orthopaedic Surgery, Orthopaedic Research Laboratories, Boston Children's Hospital, Boston, Massachusetts.
  • Vivero MP; Department of Plastic and Oral Surgery, Boston Children's Hospital, Boston, Massachusetts.
  • Hall AM; Department of Anesthesia, Boston Children's Hospital, Boston, Massachusetts.
  • Zurakowski D; Department of Anesthesia, Boston Children's Hospital, Boston, Massachusetts.
  • Adams D; Division of Hematology/Oncology, Department of Medicine, Boston Children's Hospital, Boston, Massachusetts.
  • Gupta A; Department of Pathology and Lab Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio.
  • Huang AY; Department of Orthopaedic Surgery, Orthopaedic Research Laboratories, Boston Children's Hospital, Boston, Massachusetts.
  • Chung BHY; Department of Paediatrics and Adolescent Medicine, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
  • Warman ML; Department of Orthopaedic Surgery, Orthopaedic Research Laboratories, Boston Children's Hospital, Boston, Massachusetts.
Clin Genet ; 93(5): 1075-1080, 2018 05.
Article em En | MEDLINE | ID: mdl-29231959
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Síndrome de Klippel-Trenaunay-Weber / Tumor de Wilms / Malformações Vasculares / Classe I de Fosfatidilinositol 3-Quinases / Lipoma / Anormalidades Musculoesqueléticas / Nevo Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Revista: Clin Genet Ano de publicação: 2018 Tipo de documento: Article
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Síndrome de Klippel-Trenaunay-Weber / Tumor de Wilms / Malformações Vasculares / Classe I de Fosfatidilinositol 3-Quinases / Lipoma / Anormalidades Musculoesqueléticas / Nevo Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male / Middle aged Idioma: En Revista: Clin Genet Ano de publicação: 2018 Tipo de documento: Article