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Human Genetics|January 1, 1995
Evidence for an iduronate-sulfatase pseudogene near the functional Hunter syndrome gene in Xq27.3-q28M Rathmann, S Bunge, C Steglich, et al.
Ultrastructural Pathology|January 1, 1987
Diagnostic electron microscopy using fine needle aspiration biopsiesB Mackay, T Fanning, J M Bruner, et al.
Somatic Cell Genetics|March 1, 1980
Expression of human genes for adenine phosphoribosyltransferase and hypoxanthine-guanine phosphoribosyltransferase after genetic transformation of mouse cells with purified human DNAS C Lester, S K LeVan, C Steglich, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 1, 1981
Cell cycle-dependent regulation of thymidine kinase activity introduced into mouse LMTK- cells by DNA and chromatin-mediated gene transferC A Schlosser, C Steglich, J R deWet, et al.
Experimental Brain Research|March 13, 1998
The time course of cross-talk during the simultaneous specification of bimanual movement amplitudesH Heuer, W Spijkers, T Kleinsorge, et al.
American Journal of Medical Genetics|September 1, 1992
Deletion of the Hunter gene and both DXS466 and DXS304 in a patient with mucopolysaccharidosis type IIM Beck, C Steglich, B Zabel, et al.
Human Molecular Genetics|August 1, 1992
Mutation analysis of the iduronate-2-sulfatase gene in patients with mucopolysaccharidosis type II (Hunter syndrome)S Bunge, C Steglich, M Beck, et al.
Prenatal Diagnosis|September 1, 1994
Prenatal diagnosis and carrier detection in mucopolysaccharidosis type II by mutation analysis. A 47,XXY male heterozygous for a missense point mutationS Bunge, C Steglich, P Lorenz, et al.
European Journal of Human Genetics : EJHG|November 5, 1998
Homologous nonallelic recombinations between the iduronate-sulfatase gene and pseudogene cause various intragenic deletions and inversions in patients with mucopolysaccharidosis type IIS Bunge, M Rathmann, C Steglich, et al.
Journal of Medical Genetics|February 9, 1999
Mucopolysaccharidosis type IIIB (Sanfilippo B): identification of 18 novel alpha-N-acetylglucosaminidase gene mutationsS Bunge, A Knigge, C Steglich, et al.
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