Refinement of the critical region in a new 7p22.1 microduplication syndrome including craniofacial dysmorphism and speech delay

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Bibliographische Detailangaben
Veröffentlicht in:	American journal of medical genetics. Part A 2014-11, Vol.164A (11), p.2964-2967
Hauptverfasser:	Pebrel-Richard, Celine, Rouzade, Charles, Kemeny, Stephan, Eymard-Pierre, Eleonore, Gay-Bellile, Mathilde, Gouas, Laetitia, Tchirkov, Andreï, Goumy, Carole, Vago, Philippe
Format:	Artikel
Sprache:	eng
Schlagworte:	7p22.1 microduplication ACTB Child, Preschool Chromosome Duplication Chromosomes, Human, Pair 7 Comparative Genomic Hybridization Craniofacial Abnormalities - diagnosis Craniofacial Abnormalities - genetics craniofacial dysmorphism Facies Humans intellectual disability Language Development Disorders - diagnosis Language Development Disorders - genetics Male Phenotype Syndrome
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