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Noonan syndrome with multiple lentigines and associated craniosynostosis.
McDonald, B S; Pigors, M; Kelsell, D P; O'Toole, E A; Burkitt-Wright, E; Kerr, B; Batta, K.
Afiliação
  • McDonald BS; Department of Dermatology, Watford General Hospital, Hertfordshire Hospitals NHS Trust, Watford, Hertfordshire, UK.
  • Pigors M; Centre for Cell Biology and Cutaneous Research, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Kelsell DP; Centre for Cell Biology and Cutaneous Research, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • O'Toole EA; Centre for Cell Biology and Cutaneous Research, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Burkitt-Wright E; Manchester Centre for Genomic Medicine, Genetic Medicine, St Mary's Hospital, Central Manchester University Hospitals NHS Foundation Trust, Manchester, UK.
  • Kerr B; Manchester Centre for Genomic Medicine, Genetic Medicine, St Mary's Hospital, Central Manchester University Hospitals NHS Foundation Trust, Manchester, UK.
  • Batta K; Department of Dermatology, Watford General Hospital, Hertfordshire Hospitals NHS Trust, Watford, Hertfordshire, UK.
Clin Exp Dermatol ; 43(3): 357-359, 2018 Apr.
Article em En | MEDLINE | ID: mdl-29356064

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Craniossinostoses / Síndrome LEOPARD Tipo de estudo: Risk_factors_studies Limite: Child / Humans / Male Idioma: En Revista: Clin Exp Dermatol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Craniossinostoses / Síndrome LEOPARD Tipo de estudo: Risk_factors_studies Limite: Child / Humans / Male Idioma: En Revista: Clin Exp Dermatol Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Reino Unido