Breakpoint Cloning and Haplotype Analysis Indicate a Single Origin of the Common Inv(10)(p11.2q21.2) Mutation among Northern Europeans

✍ Scribed by Mette Gilling; Jörn S. Dullinger; Stefan Gesk; Simone Metzke-Heidemann; Reiner Siebert; Thomas Meyer; Karen Brondum-Nielsen; Niels Tommerup; Hans-Hilger Ropers; Zeynep Tümer; Vera M. Kalscheuer; N. Simon Thomas

• Book ID: 117854796
• Publisher: American Society of Human Genetics
• Year: 2006
• Tongue: English
• Weight: 384 KB
• Volume: 78
• Category: Article
• ISSN: 0002-9297
• DOI: 10.1086/503632