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


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


The American Journal of Human Genetics




May 2006

Copyright © 2006, Elsevier

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