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Hypersociability associated with developmental delay, macrocephaly and facial dysmorphism points to CHD3 mutations.

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Bibliographic Details
Title: Hypersociability associated with developmental delay, macrocephaly and facial dysmorphism points to CHD3 mutations.
Authors: Coursimault J; Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, Department of Genetics and reference center for developmental disorders, FHU G4 Génomique, F-76000 Rouen, France., Lecoquierre F; Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, Department of Genetics and reference center for developmental disorders, FHU G4 Génomique, F-76000 Rouen, France., Saugier-Veber P; Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, Department of Genetics and reference center for developmental disorders, FHU G4 Génomique, F-76000 Rouen, France., Drouin-Garraud V; Department of Pediatrics, Rouen University Hospital, F-76000, Rouen, France., Lechevallier J; Department of Pediatric Surgery, Rouen University Hospital, F-76000, Rouen, France., Boland A; Centre National de Recherche en Génomique Humaine, Institut de Biologie François Jacob, CEA, Université Paris-Saclay, Evry, France., Deleuze JF; Centre National de Recherche en Génomique Humaine, Institut de Biologie François Jacob, CEA, Université Paris-Saclay, Evry, France., Frebourg T; Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, Department of Genetics and reference center for developmental disorders, FHU G4 Génomique, F-76000 Rouen, France., Nicolas G; Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, Department of Genetics and reference center for developmental disorders, FHU G4 Génomique, F-76000 Rouen, France., Brehin AC; Normandie Univ, UNIROUEN, Inserm U1245, CHU Rouen, Department of Genetics and reference center for developmental disorders, FHU G4 Génomique, F-76000 Rouen, France. Electronic address: anne-claire.brehin@chu-rouen.fr.
Source: European journal of medical genetics [Eur J Med Genet] 2021 Apr; Vol. 64 (4), pp. 104166. Date of Electronic Publication: 2021 Feb 09.
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 101247089 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1878-0849 (Electronic) Linking ISSN: 17697212 NLM ISO Abbreviation: Eur J Med Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1878-0849
DOI:10.1016/j.ejmg.2021.104166