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Molecular Microbiology|January 1, 1989
Three alpha-amylase genes of Aspergillus oryzae exhibit identical intron-exon organizationS Wirsel, A Lachmund, G Wildhardt, et al.
Thyroid : Official Journal of the American Thyroid Association|February 1, 1997
Resistance to thyroid hormone in a family caused by a new point mutation L330S in the thyroid receptor (TR) beta geneJ Pohlenz, G Wildhardt, B Zabel, et al.
Rheumatology International|June 24, 2009
A monoallelic double mutation as a cause for TNF receptor-associated periodic fever syndromeJ Trübenbach, G Wildhardt, J Niebel, et al.
Oncogene|July 1, 1992
RNA polymerase chain reaction detects different levels of four alternatively spliced WT1 transcripts in Wilms' tumorsB Brenner, G Wildhardt, S Schneider, et al.
Human Genetics|July 1, 1993
Exon skipping due to a mutation in a donor splice site in the WT-1 gene is associated with Wilms' tumor and severe genital malformationsS Schneider, G Wildhardt, R Ludwig, et al.
Molecular and Cellular Probes|June 1, 1996
Two different PAX3 gene mutations causing Waardenburg syndrome type IG Wildhardt, A Winterpacht, K Hilbert, et al.
American Journal of Medical Genetics. Part A|November 13, 2007
A familial case of achondrogenesis type II caused by a dominant COL2A1 mutation and "patchy" expression in the mosaic fatherF Forzano, M Lituania, A Viassolo, et al.
Klinische Padiatrie|April 18, 2001
[Present limitations of molecular biological diagnostics in Gillespie syndrome]M Kieslich, K Vanselow, G Wildhardt, et al.
Der Ophthalmologe : Zeitschrift Der Deutschen Ophthalmologischen Gesellschaft|February 20, 1999
[Molecular genetic study of the PAX6 gene in aniridia patients]M Wolf, B Zabel, B Lorenz, et al.
Cytogenetics and Cell Genetics|January 21, 2000
Genomic structure, alternative transcripts and chromosome location of the human LIM domain binding protein 1 gene LDB1M Drechsler, V Schumacher, S Friedrich, et al.
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