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Clinical Presentation of a Complex Neurodevelopmental Disorder Caused by Mutations in ADNP.
Van Dijck, Anke; Vulto-van Silfhout, Anneke T; Cappuyns, Elisa; van der Werf, Ilse M; Mancini, Grazia M; Tzschach, Andreas; Bernier, Raphael; Gozes, Illana; Eichler, Evan E; Romano, Corrado; Lindstrand, Anna; Nordgren, Ann; Kvarnung, Malin; Kleefstra, Tjitske; de Vries, Bert B A; Küry, Sébastien; Rosenfeld, Jill A; Meuwissen, Marije E; Vandeweyer, Geert; Kooy, R Frank.
Affiliation
  • Van Dijck A; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium; Department of Neurology, University Hospital Antwerp, Antwerp, Belgium. Electronic address: anke.vandijck@uantwerpen.be.
  • Vulto-van Silfhout AT; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Cappuyns E; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
  • van der Werf IM; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
  • Mancini GM; Department of Clinical Genetics, Erasmus Medical Center, Rotterdam, the Netherlands.
  • Tzschach A; Institute für Klinische Genetik, Technische Universität Dresden, Dresden, Germany.
  • Bernier R; Department of Psychiatry, University of Washington, Seattle, Washington.
  • Gozes I; Elton Laboratory for Molecular Neuroendocrinology, Tel Aviv University, Tel Aviv, Israel; Department of Human Molecular Genetics and Biochemistry, Sackler Faculty of Medicine, Sagol School of Neuroscience, Tel Aviv University, Tel Aviv, Israel; Adams Super Center for Brain Studies, Tel Aviv Universi
  • Eichler EE; Department of Genome Sciences, University of Washington, Seattle, Washington; Howard Hughes Medical Institute, University of Washington, Seattle, Washington.
  • Romano C; Unit of Pediatrics and Medical Genetics, Istituto di Ricovero e Cura a Carattere Scientifico Associazione Oasi Maria Santissima, Troina, Italy.
  • Lindstrand A; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
  • Nordgren A; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
  • Kvarnung M; Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
  • Kleefstra T; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.
  • de Vries BBA; Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.
  • Küry S; Service de Génétique Médicale, Centre Hospitalier Universitaire Nantes, Nantes, France.
  • Rosenfeld JA; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas.
  • Meuwissen ME; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
  • Vandeweyer G; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
  • Kooy RF; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
Biol Psychiatry ; 85(4): 287-297, 2019 02 15.
Article in En | MEDLINE | ID: mdl-29724491
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Homeodomain Proteins / Neurodevelopmental Disorders / Nerve Tissue Proteins Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Biol Psychiatry Year: 2019 Document type: Article Country of publication: Estados Unidos
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Homeodomain Proteins / Neurodevelopmental Disorders / Nerve Tissue Proteins Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Qualitative_research / Risk_factors_studies Limits: Adolescent / Adult / Child / Child, preschool / Female / Humans / Infant / Male Language: En Journal: Biol Psychiatry Year: 2019 Document type: Article Country of publication: Estados Unidos