Angela M. Kaindl

Homozygous microdeletion of chromosome 4q11‐q12 causes severe limb‐girdle muscular dystrophy type 2E with joint hyperlaxity and contractures

J. Weis, K. Koehler, A. Huebner, 2005, Human mutation.

Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation‐dependent probe amplification

A. Lang, P. Pramstaller, P. Vieregge, 2007, Movement disorders : official journal of the Movement Disorder Society.