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Clinical and genomic delineation of the new proximal 19p13.3 microduplication syndrome.

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Title: Clinical and genomic delineation of the new proximal 19p13.3 microduplication syndrome.
Authors: Jouret G; Department of Genetics, Reims University Hospital, Reims, France.; National Center of Genetics (NCG), Laboratoire national de santé (LNS), Dudelange, Luxembourg., Egloff M; Department of Genetics, Necker-Enfants malades, AP-HP, Institut Imagine, Paris, France., Landais E; Department of Genetics, Reims University Hospital, Reims, France., Tassy O; IGBMC, Strasbourg, France., Giuliano F; Department of Genetics, Nice University Hospital, Nice, France., Karmous-Benailly H; Department of Genetics, Nice University Hospital, Nice, France., Coutton C; Service de Génétique et Procréation, Hôpital Couple-Enfant, CHU Grenoble Alpes, Université Grenoble-Alpes, La Tronche, France.; ACLF (Association des Cytogénéticiens de Langue Française, French Society of Cytogenetics) Member, Grenoble cedex, France., Satre V; Service de Génétique et Procréation, Hôpital Couple-Enfant, CHU Grenoble Alpes, Université Grenoble-Alpes, La Tronche, France., Devillard F; Service de Génétique et Procréation, Hôpital Couple-Enfant, CHU Grenoble Alpes, Université Grenoble-Alpes, La Tronche, France., Dieterich K; Service de Génétique et Procréation, Hôpital Couple-Enfant, CHU Grenoble Alpes, Université Grenoble-Alpes, La Tronche, France., Vieville G; Service de Génétique et Procréation, Hôpital Couple-Enfant, CHU Grenoble Alpes, Université Grenoble-Alpes, La Tronche, France., Kuentz P; Génétique Biologique, PCBio, Besançon University Hospital, Besançon, France., le Caignec C; ACLF (Association des Cytogénéticiens de Langue Française, French Society of Cytogenetics) Member, Grenoble cedex, France.; Department of Genetics, Nantes University Hospital, Nantes, France., Beneteau C; Department of Genetics, Nantes University Hospital, Nantes, France., Isidor B; Department of Genetics, Nantes University Hospital, Nantes, France., Nizon M; Department of Genetics, Nantes University Hospital, Nantes, France., Callier P; ACLF (Association des Cytogénéticiens de Langue Française, French Society of Cytogenetics) Member, Grenoble cedex, France.; Department of Genetics, Dijon University Hospital, Dijon, France., Marquet V; ACLF (Association des Cytogénéticiens de Langue Française, French Society of Cytogenetics) Member, Grenoble cedex, France.; Department of Genetics, Limoges University Hospital, Limoges, France., Bieth E; Department of Genetics, Toulouse University Hospital, Toulouse, France., Lévy J; Department of Genetics, Robert-Debré University Hospital, Paris, France., Tabet AC; Department of Genetics, Robert-Debré University Hospital, Paris, France., Lyonnet S; Department of Genetics, Necker-Enfants malades, AP-HP, Institut Imagine, Paris, France.; INSERM U-1163, Université de Paris, Paris, France., Baujat G; Department of Genetics, Necker-Enfants malades, AP-HP, Institut Imagine, Paris, France., Rio M; Department of Genetics, Necker-Enfants malades, AP-HP, Institut Imagine, Paris, France., Cartault F; Department of Genetics, La Réunion University Hospital, Saint Denis, France., Scheidecker S; Strasbourg University Hospital, Strasbourg, France., Gouronc A; Strasbourg University Hospital, Strasbourg, France., Schalk A; Strasbourg University Hospital, Strasbourg, France., Jacquin C; Department of Genetics, Reims University Hospital, Reims, France., Spodenkiewicz M; Department of Genetics, Reims University Hospital, Reims, France., Angélini C; CHU Bordeaux, Service de Génétique Médicale, Bordeaux, France., Pennamen P; CHU Bordeaux, Service de Génétique Médicale, Bordeaux, France., Rooryck C; CHU Bordeaux, Service de Génétique Médicale, Bordeaux, France., Doco-Fenzy M; Department of Genetics, Reims University Hospital, Reims, France.; ACLF (Association des Cytogénéticiens de Langue Française, French Society of Cytogenetics) Member, Grenoble cedex, France.; EA3801, SFR CAPSANTE, Reims, France., Poirsier C; Department of Genetics, Reims University Hospital, Reims, France.
Source: American journal of medical genetics. Part A [Am J Med Genet A] 2023 Jan; Vol. 191 (1), pp. 52-63. Date of Electronic Publication: 2022 Oct 05.
Publication Type: Journal Article
Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Database: MEDLINE Ultimate
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Description
ISSN:1552-4833
DOI:10.1002/ajmg.a.62983