Homozygous deletion of a gene-free region of 4p15 in a child with multiple anomalies: Could biallelic loss of conserved, non-coding elements lead to a phenotype?

✍ Scribed by Periklis Makrythanasis; Stefania Gimelli; Frédérique Béna; Sophie Dahoun; Michael A. Morris; Stylianos E. Antonarakis; Armand Bottani

• Book ID: 116433433
• Publisher: Elsevier Science
• Year: 2012
• Tongue: English
• Weight: 938 KB
• Volume: 55
• Category: Article
• ISSN: 1769-7212
• DOI: 10.1016/j.ejmg.2011.11.001