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

20 Citationer (Scopus)
1032 Downloads (Pure)

Abstract

Udgivelsesdato: 2006/5
OriginalsprogEngelsk
TidsskriftAmerican Journal of Human Genetics
Vol/bind78
Udgave nummer5
Sider (fra-til)878-883
Antal sider5
ISSN0002-9297
StatusUdgivet - 2006

Citationsformater