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Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)(p11.2q21.2) mutation among Northern Europeans
Authors: Gilling, Mette; Dullinger, Jörn S.; Gesk, Stefan; Metzke-Heidemann, Simone; Siebert, Reiner; Meyer, Thomas; Brondum-Nielsen, Karen; Tommerup, Niels; Ropers, Hans-Hilger; Tümer, Zeynep; Kalscheuer, Vera M.; Thomas, N. Simon
Date of Publication (YYYY-MM-DD): 2006-03-17
Title of Journal: American Journal of Human Genetics : AJHG / American Society of Human Genetics
Volume: 78
Issue / Number: 5
Start Page: 878
End Page: 883
Document Type: Article
ID: 307626.0
 
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