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Ureteropelvic junction obstruction with primary lymphoedema associated with CELSR1 variants.
Alpaslan, Murat; Mestré-Godin, Sandrine; Lay, Aurélie; Giacalone, Guido; Helaers, Raphaël; Adham, Salma; Kovacsik, Hélène; Guillemard, Sophie; Mercier, Erick; Boon, Laurence; Revencu, Nicole; Brouillard, Pascal; Quere, Isabelle; Vikkula, Miikka.
Afiliación
  • Alpaslan M; Human Molecular Genetics, de Duve Institute, Brussels, Belgium.
  • Mestré-Godin S; Department of vascular medicine, CHU Montpellier, Montpellier, France.
  • Lay A; IDESP - Institut Desbrest d'Épidémiologie et de Santé Publique, Montpellier, France.
  • Giacalone G; Department of vascular medicine, CHU Montpellier, Montpellier, France.
  • Helaers R; Department of Lymphatic Surgery, VASCERN PPL European Reference Centre, General Hospital Sint-Maarten, Mechelen, Belgium.
  • Adham S; Human Molecular Genetics, de Duve Institute, Brussels, Belgium.
  • Kovacsik H; Department of vascular medicine, CHU Montpellier, Montpellier, France.
  • Guillemard S; IDESP - Institut Desbrest d'Épidémiologie et de Santé Publique, Montpellier, France.
  • Mercier E; Department of vascular medicine, CHU Montpellier, Montpellier, France.
  • Boon L; Department of Nuclear Medicine, Montpellier Regional Cancer Institute, Montpellier, France.
  • Revencu N; IDESP - Institut Desbrest d'Épidémiologie et de Santé Publique, Montpellier, France.
  • Brouillard P; Hematology Laboratory, University Hospital Centre Nimes, Nimes, France.
  • Quere I; Human Molecular Genetics, de Duve Institute, Brussels, Belgium.
  • Vikkula M; Center for Vascular Anomalies, Division of Plastic Surgery, VASCERN VASCA European Reference Centre, Cliniques universitaires Saint-Luc, Brussels, Belgium.
J Med Genet ; 60(12): 1161-1168, 2023 Nov 27.
Article en En | MEDLINE | ID: mdl-37225411
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastornos de los Cromosomas / Linfedema Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: J Med Genet Año: 2023 Tipo del documento: Article País de afiliación: Bélgica
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Trastornos de los Cromosomas / Linfedema Tipo de estudio: Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Revista: J Med Genet Año: 2023 Tipo del documento: Article País de afiliación: Bélgica