Breakpoint cloning and haplotype analysis indicate a single origin of the common Inv(10)( p11.2q21.2) mutation among northern Europeans

Mette Gilling, J.S. Dullinger, S. Gesk, S. Metzke-Heidemann, R. Siebert, T. Meyer, K. Brondum-Nielsen, Niels Tommerup, H.H. Ropers, Zeynep Tümer, V.M. Kalscheuer, N.S. Thomas

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Abstract

Udgivelsesdato: 2006/5
Original languageEnglish
JournalAmerican Journal of Human Genetics
Volume78
Issue number5
Pages (from-to)878-883
Number of pages5
ISSN0002-9297
Publication statusPublished - 2006

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