Your browser doesn't support javascript.
loading
Phenotype-genotype relations in facioscapulohumeral muscular dystrophy type 1.
Mul, Karlien; Voermans, Nicol C; Lemmers, Richard J L F; Jonker, Marianne A; van der Vliet, Patrick J; Padberg, George W; van Engelen, Baziel G M; van der Maarel, Silvère M; Horlings, Corinne G C.
Affiliation
  • Mul K; Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Voermans NC; Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Lemmers RJLF; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Jonker MA; Department of Health Evidence, Radboud University Medical Center, Nijmegen, The Netherlands.
  • van der Vliet PJ; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Padberg GW; Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • van Engelen BGM; Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
  • van der Maarel SM; Department of Human Genetics, Leiden University Medical Center, Leiden, The Netherlands.
  • Horlings CGC; Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.
Clin Genet ; 94(6): 521-527, 2018 12.
Article de En | MEDLINE | ID: mdl-30211448
Sujet(s)
Mots clés
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Phénotype / Prédisposition génétique à une maladie / Dystrophie musculaire facio-scapulo-humérale / Études d'associations génétiques / Génotype Type d'étude: Prognostic_studies Limites: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Langue: En Journal: Clin Genet Année: 2018 Type de document: Article Pays d'affiliation: Pays-Bas Pays de publication: Danemark
Texte intégral
Ajouter à My VHL
Imprimer
XML
PubMed Links
Recherche sur Google

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Phénotype / Prédisposition génétique à une maladie / Dystrophie musculaire facio-scapulo-humérale / Études d'associations génétiques / Génotype Type d'étude: Prognostic_studies Limites: Adolescent / Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Langue: En Journal: Clin Genet Année: 2018 Type de document: Article Pays d'affiliation: Pays-Bas Pays de publication: Danemark