G. Wildhardt

Cancer spectrum and frequency among children with Noonan, Costello, and cardio-facio-cutaneous syndromes

Christian P. Kratz, Lude Franke, Harm Peters et al. · British Journal of Cancer · 2015 · 207 citations · Full text

Enhancer deletions of the <i>SHOX</i> gene as a frequent cause of short stature: the essential role of a 250 kb downstream regulatory domain

J Chen, G. Wildhardt, Zeyan Zhong et al. · Journal of Medical Genetics · 2009 · 130 citations · Full text

Correlation of germ-line mutations and two-hit inactivation of the <i>WT1</i> gene with Wilms tumors of stromal–predominant histology

Valerié Schumacher, Susanne A. Schneider, A. Figge et al. · Proceedings of the National Academy of Sciences · 1997 · 130 citations

Three α‐amylase genes of <i>Aspergillus oryzae</i> exhibit identical intron‐exon organization

Stefan G. R. Wirsel, Astrid Lachmund, G. Wildhardt et al. · Molecular Microbiology · 1989 · 73 citations

Ten novel mutations found in aniridia

Matthias T. F. Wolf, Birgit Lorenz, Andreas Winterpacht et al. · Human Mutation · 1998 · 46 citations

Ocular Disease, Genetics, Molecular Genetics +16