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Familial progressive hyper- and hypopigmentation and malignancy in two families with new mutations in KITLG.
Cuell, A; Bansal, N; Cole, T; Kaur, M R; Lee, J; Loffeld, A; Moss, C; O'Donnell, M; Takeichi, T; Thind, C K; McGrath, J A.
Afiliación
  • Cuell A; Department of Dermatology, Birmingham Children's Hospital, NHS Foundation Trust, Birmingham, UK.
  • Bansal N; Department of Dermatology, Solihull Hospital, Heart of England NHS Foundation Trust, Solihull, UK.
  • Cole T; Department of Clinical Genetics, Birmingham Women's Hospital, NHS Foundation Trust, Birmingham, UK.
  • Kaur MR; Department of Dermatology, Solihull Hospital, Heart of England NHS Foundation Trust, Solihull, UK.
  • Lee J; Genetic Skin Disease Group, St John's Institute of Dermatology, King's College London, London, UK.
  • Loffeld A; Department of Dermatology, Solihull Hospital, Heart of England NHS Foundation Trust, Solihull, UK.
  • Moss C; Department of Dermatology, Birmingham Children's Hospital, NHS Foundation Trust, Birmingham, UK.
  • O'Donnell M; Department of Clinical Genetics, Birmingham Women's Hospital, NHS Foundation Trust, Birmingham, UK.
  • Takeichi T; Genetic Skin Disease Group, St John's Institute of Dermatology, King's College London, London, UK.
  • Thind CK; Department of Dermatology, Birmingham Children's Hospital, NHS Foundation Trust, Birmingham, UK.
  • McGrath JA; Genetic Skin Disease Group, St John's Institute of Dermatology, King's College London, London, UK.
Clin Exp Dermatol ; 40(8): 860-4, 2015 Dec.
Article en En | MEDLINE | ID: mdl-26179221
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hipopigmentación / Hiperpigmentación / Factor de Células Madre / Mutación Missense Tipo de estudio: Prognostic_studies Límite: Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Exp Dermatol Año: 2015 Tipo del documento: Article País de afiliación: Reino Unido
Texto completo
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XML
PubMed Links
Buscar en Google

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Hipopigmentación / Hiperpigmentación / Factor de Células Madre / Mutación Missense Tipo de estudio: Prognostic_studies Límite: Adult / Child / Child, preschool / Female / Humans / Male / Middle aged Idioma: En Revista: Clin Exp Dermatol Año: 2015 Tipo del documento: Article País de afiliación: Reino Unido