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Expanding the clinical spectrum of biallelic ZNF335 variants.
Stouffs, K; Stergachis, A B; Vanderhasselt, T; Dica, A; Janssens, S; Vandervore, L; Gheldof, A; Bodamer, O; Keymolen, K; Seneca, S; Liebaers, I; Jayaraman, D; Hill, H E; Partlow, J N; Walsh, C A; Jansen, A C.
Affiliation
  • Stouffs K; Center for Medical Genetics, UZ Brussel, Brussels, Belgium.
  • Stergachis AB; Neurogenetics Research Unit, Reproduction Genetics and Regenerative Medicine, Vrije Universiteit Brussel, Brussels, Belgium.
  • Vanderhasselt T; Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
  • Dica A; Department of Radiology, UZ Brussel, Brussels, Belgium.
  • Janssens S; Pediatric Neurology Clinic, Alexandru Obregia Hospital, Bucharest, Romania.
  • Vandervore L; Centre for Medical Genetics, Ghent University Hospital, Ghent, Belgium.
  • Gheldof A; Neurogenetics Research Unit, Reproduction Genetics and Regenerative Medicine, Vrije Universiteit Brussel, Brussels, Belgium.
  • Bodamer O; Center for Medical Genetics, UZ Brussel, Brussels, Belgium.
  • Keymolen K; Neurogenetics Research Unit, Reproduction Genetics and Regenerative Medicine, Vrije Universiteit Brussel, Brussels, Belgium.
  • Seneca S; Division of Genetics and Genomics, Department of Medicine, Boston Children's Hospital, Harvard Medical School, Boston, Massachusetts.
  • Liebaers I; Center for Medical Genetics, UZ Brussel, Brussels, Belgium.
  • Jayaraman D; Neurogenetics Research Unit, Reproduction Genetics and Regenerative Medicine, Vrije Universiteit Brussel, Brussels, Belgium.
  • Hill HE; Center for Medical Genetics, UZ Brussel, Brussels, Belgium.
  • Partlow JN; Neurogenetics Research Unit, Reproduction Genetics and Regenerative Medicine, Vrije Universiteit Brussel, Brussels, Belgium.
  • Walsh CA; Center for Medical Genetics, UZ Brussel, Brussels, Belgium.
  • Jansen AC; Division of Genetics and Genomics, Department of Medicine, Boston Children's Hospital, Boston, Massachusetts.
Clin Genet ; 94(2): 246-251, 2018 08.
Article de En | MEDLINE | ID: mdl-29652087
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Protéines nucléaires / Protéines et peptides de signalisation intracellulaire / Neurogenèse / Microcéphalie / Dégénérescence nerveuse Type d'étude: Prognostic_studies Limites: Female / Humans / Infant / Male / Newborn Langue: En Journal: Clin Genet Année: 2018 Type de document: Article Pays d'affiliation: Belgique
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: Protéines nucléaires / Protéines et peptides de signalisation intracellulaire / Neurogenèse / Microcéphalie / Dégénérescence nerveuse Type d'étude: Prognostic_studies Limites: Female / Humans / Infant / Male / Newborn Langue: En Journal: Clin Genet Année: 2018 Type de document: Article Pays d'affiliation: Belgique