Your browser doesn't support javascript.
loading
New insights on the clinical variability of FKBP10 mutations.
Essawi, Osama H; Tapaneeyaphan, Piyanoot; Symoens, Sofie; Gistelinck C, Charlotte; Malfait, Fransiska; Eyre, David R; Essawi, Tamer; Callewaert, Bert; Coucke, Paul J.
Afiliación
  • Essawi OH; Department Master Program in Clinical Laboratory Science, Birzeit University, Palestine; Center for Medical Genetics, Ghent University, Ghent, Belgium. Electronic address: osama.essawi@Ugent.be.
  • Tapaneeyaphan P; Center for Medical Genetics, Ghent University, Ghent, Belgium.
  • Symoens S; Center for Medical Genetics, Ghent University, Ghent, Belgium.
  • Gistelinck C C; Department of Orthopaedics and Sports Medicine, University of Washington, Seattle, WA, USA.
  • Malfait F; Center for Medical Genetics, Ghent University, Ghent, Belgium.
  • Eyre DR; Department of Orthopaedics and Sports Medicine, University of Washington, Seattle, WA, USA.
  • Essawi T; Department Master Program in Clinical Laboratory Science, Birzeit University, Palestine.
  • Callewaert B; Center for Medical Genetics, Ghent University, Ghent, Belgium.
  • Coucke PJ; Center for Medical Genetics, Ghent University, Ghent, Belgium.
Eur J Med Genet ; 63(9): 103980, 2020 Sep.
Article en En | MEDLINE | ID: mdl-32531462
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteogénesis Imperfecta / Fenotipo / Artrogriposis / Proteínas de Unión a Tacrolimus / Mutación Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article Pais de publicación: Países Bajos
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Osteogénesis Imperfecta / Fenotipo / Artrogriposis / Proteínas de Unión a Tacrolimus / Mutación Límite: Adolescent / Adult / Child / Female / Humans / Male Idioma: En Revista: Eur J Med Genet Asunto de la revista: GENETICA MEDICA Año: 2020 Tipo del documento: Article Pais de publicación: Países Bajos