D. Schindler

发表

Shared Copy Number Variation in Simultaneous Nephroblastoma and Neuroblastoma due to Fanconi Anemia

T. Barth, K. Mrasek, T. Liehr, 2012, Molecular Syndromology.

Simultaneous measurement, using flow cytometry, of radiosensitivity and defective mitogen response in ataxia telangiectasia and related syndromes

F. Hanefeld, I. Krägeloh-Mann, J. Fryns, 1992, European Journal of Pediatrics.

Elevated oxidative stress in patients with ataxia telangiectasia.

R. Schubert, S. Zielen, J. Reichenbach, 2002, Antioxidants & redox signaling.

Characterization of ATM gene mutations in 66 ataxia telangiectasia families.

T. Dörk, Y. Shiloh, A. Rosenthal, 1999, Human molecular genetics.

Chromosome instability and X-ray hypersensitivity in a microcephalic and growth-retarded child.

H. Seyschab, D. Schindler, K. Mehnert, 1991, American journal of medical genetics.

Physical mapping of the holoprosencephaly critical region on chromosome 7q36

B. Trask, S. Scherer, L. Tsui, 1993, Nature Genetics.

Clinical Investigation

A. Rosenthal, M. Platzer, H. Hoehn, 2003, Advances in Experimental Medicine and Biology.

Unusual mutations in high functioning fragile X males: apparent instability of expanded unmethylated CGG repeats.

W. Vogel, W. Vogel, D. Gläser, 1998, Journal of medical genetics.

Recurrent mutation pressure does not explain the prevalence of the marker (X) syndrome

F. Vogel, J. Fryns, E. Schwinger, 2004, Human Genetics.