Developmental delay and facial dysmorphism in a child with an 8.9 Mb de novo interstitial deletion of 3q25.1–q25.32: Genotype–phenotype correlations of chromosome 3q25 deletion syndrome

✍ Scribed by Stephanie Moortgat; Christine Verellen-Dumoulin; Isabelle Maystadt; Benoit Parmentier; Bernard Grisart; Jean-Luc Hennecker; Anne Destree

• Book ID: 116433342
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 423 KB
• Volume: 54
• Category: Article
• ISSN: 1769-7212
• DOI: 10.1016/j.ejmg.2010.11.011