A. Ehrbrecht

Comprehensive genomic analysis of desmoplastic medulloblastomas: identification of novel amplified genes and separate evaluation of the different histological components

A. Hoischen, M. Wolter, G. Reifenberger, 2006, The Journal of pathology.

Homozygous mutations in caveolin‐3 cause a severe form of rippling muscle disease

T. Brüning, J. Malin, H. Goebel, 2003, Annals of neurology.

Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations.

A. Hoischen, P. Propping, H. Engels, 2002, American journal of medical genetics.

Further delineation of the phenotype maps for partial trisomy 16q24 and Jacobsen syndrome by a subtle familial translocation t(11;16)(q24.2;q24.1)

V. Kalscheuer, P. Propping, B. Albrecht, 2005, American Journal of Medical Genetics. Part A.

Comprehensive analysis of human subtelomeres with combined binary ratio labelling fluorescence in situ hybridisation

H. Tanke, H. Vrolijk, J. Wiegant, 2003, European Journal of Human Genetics.

Global brain dysmyelination with above‐average verbal skills in 18q − syndrome with a 17 Mb terminal deletion

H. Urbach, C. Helmstaedter, H. Engels, 2006, Acta neurologica Scandinavica.