U. Klein-Vogler

Exclusion of the GABAA-receptor β3 subunit gene as the Angelman's syndrome gene

G. Niemann, H. Enders, J. Kunze, 1993, The Lancet.

Molecular and cytogenate analysis of an X/autosomal translocation: 45, X, dic(X;17)(p22.2;p13)

T. Eggermann, L. Sieverding, H. Enders, 1998 .

Bibliography of Ulrich Wolf

C. Tyler-Smith, P. Yen, K. Hirschhorn, 2001, Cytogenetic and Genome Research.

Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level

V. Maloney, J. Barber, A. Dufke, 2005, European Journal of Human Genetics.

Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome

A. Dufke, T. Liehr, M. Schöning, 2001, Cytogenetic and Genome Research.

Pitfall: Amniocentesis fails to detect mosaic trisomy 8 in a male newborn

M. Leipold, J. Tomiuk, H. Enders, 1994, Prenatal diagnosis.

New case of mosaic tetrasomy 9p with additional neurometabolic findings.

T. Eggermann, H. Enders, E. Rossier, 1998, American journal of medical genetics.

Prenatal detection of double aneuploidy trisomy 10/monosomy X in a liveborn twin with exclusively monosomy X in blood

G. Mielke, U. Trautmann, R. Goelz, 1997, Clinical genetics.