G. Raabe-Meyer

Molecular karyotyping as a relevant diagnostic tool in children with growth retardation with Silver-Russell features.

A. Jauch, M. Baudis, K. Zerres, 2012, The Journal of pediatrics.

First Case of a Neocentromere Formation in an Otherwise Normal Chromosome 7

T. Liehr, A. Weise, M. Ziegler, 2009, Cytogenetic and Genome Research.

Maternal uniparental disomy of chromosome 16 [upd(16)mat]: clinical features are rather caused by (hidden) trisomy 16 mosaicism than by upd(16)mat itself

T. Eggermann, M. Elbracht, M. Begemann, 2017, Clinical genetics.

Diagnostic accuracy of random massively parallel sequencing for non‐invasive prenatal detection of common autosomal aneuploidies: a collaborative study in Europe

M. Hempel, M. Wüstemann, R. Zimmermann, 2014, Prenatal diagnosis.

Maternal uniparental disomy of chromosome 16 ( upd ( 16 ) mat ) : Clinical features are rather caused by ( hidden ) trisomy 16 mosaicism than by upd ( 16 ) mat itself

M. Elbracht, D. Meschede, Matthias Begemann, 2016 .