Fourteen new cases contribute to the characterization of the 7q11.23 microduplication syndrome Emerging Microdeletion and Microduplication Syndromes

• Published in: European journal of medical genetics Vol. 52; no. 2-3; pp. 94 - 100
• Main Authors: VAN DER AA, Nathalie, ROOMS, Liesbeth, DESTREE, Anne, MAYSTADT, Isabelle, MÄNNIK, Katrin, KURG, Ants, REIMAND, Tiia, MCMULLAN, Dom, OLEY, Christine, BRUETON, Louise, BONGERS, Ernie M. H. F, VAN BON, Bregje W. M, VANDEWEYER, Geert, PFUND, Rolph, JACQUEMONT, Sebastien, FERRARINI, Alessandra, MARTINET, Danielle, SCHRANDER-STUMPEL, Connie, STEGMANN, Alexander P. A, FRINTS, Suzanna G. M, DE VRIES, Bert B. A, CEULEMANS, Berten, KOOY, R. Frank, VAN DEN ENDE, Jenneke, REYNIERS, Edwin, FICHERA, Marco, ROMANO, Corrado, DELLE CHIAIE, Barbara, MORTIER, Geert, MENTEN, Björn
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier 2009
• Subjects: Biological and medical sciences; Disorders of higher nervous function. Focal brain diseases. Central vestibular syndrome and deafness. Brain stem syndromes; Fundamental and applied biological sciences. Psychology; General aspects. Genetic counseling; Genetics of eukaryotes. Biological and molecular evolution; Medical genetics; Medical sciences; Nervous system (semeiology, syndromes); Neurology; Human; Clinical phenotype; Language disorder; Syndrome; Recognizable face; Characterization; Case study; Communication disorder; Phenotype; Language retardation; 7q11.23 microduplication; Language delay; Genetics; Face
• ISSN: 1769-7212; 1878-0849