Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes

✍ Scribed by Bartholdi, D. (author);Krajewska-Walasek, M. (author);Õunap, K. (author);Gaspar, H. (author);Chrzanowska, K. H. (author);Ilyana, H. (author);Kayserili, H. (author);Lurie, I. W. (author);Schinzel, A. (author);Baumer, A. (author)

• Book ID: 115492991
• Publisher: BMJ Publishing Group
• Year: 2008
• Tongue: English
• Weight: 232 KB
• Volume: 46
• Category: Article
• ISSN: 0022-2593
• DOI: 10.1136/jmg.2008.061820