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European Journal of Human Genetics : EJHG|October 31, 2002
CFTR gene mutations in sarcoidosisManfred Schürmann, Melanie Albrecht, Eberhard Schwinger, et al.
BMC Medical Genetics|July 2, 2005
Spinocerebellar ataxia type 17: report of a family with reduced penetrance of an unstable Gln49 TBP allele, haplotype analysis supporting a founder effect for unstable alleles and comparative analysis of SCA17 genotypesChristine Zühlke, Andreas Dalski, Eberhard Schwinger, et al.
Schizophrenia Research|December 31, 2002
Schizophrenia spectrum disorders and eye tracking dysfunction in singleton and multiplex schizophrenia familiesRebekka Lencer, Katja Trillenberg-Krecker, Eberhard Schwinger, et al.
Journal of Neurology|February 8, 2003
Phenotypical variability of expanded alleles in the TATA-binding protein gene. Reduced penetrance in SCA17?Christine Zühlke, Ulrike Gehlken, Yorck Hellenbroich, et al.
Psychiatric Genetics|May 29, 2004
No association of the SCA1 (CAG)31 allele with Huntington's disease, myotonic dystrophy type 1 and spinocerebellar ataxia type 3Yorck Hellenbroich, Manuel Kaulich, Sven Opitz, et al.
Human Mutation|January 15, 2004
Mutations in the MATP gene in five German patients affected by oculocutaneous albinism type 4Uta Rundshagen, Christine Zühlke, Sven Opitz, et al.
Human Mutation|May 18, 2004
Detection of 53 novel DNA variations within the tyrosinase gene and accumulation of mutations in 17 patients with albinismSven Opitz, Barbara Käsmann-Kellner, Markus Kaufmann, et al.
Fetal Diagnosis and Therapy|February 11, 2003
Validation of primed in situ labeling for interphase analysis of chromosomes 18, X, and Y in uncultured amniocytesKirsten Mennicke, Jianbin Yang, Frauke Hinrichs, et al.
European Journal of Human Genetics : EJHG|April 26, 2002
Spinocerebellar ataxia type 1 (SCA1): phenotype-genotype correlation studies in intermediate allelesChristine Zühlke, Andreas Dalski, Yorck Hellenbroich, et al.
Prenatal Diagnosis|March 16, 2012
Klinefelter twins presenting with discordant aneuploidies, acardia, forked umbilical cord and with different gonadal sex despite monozygosityHelga Rehder, Katharina Schoner, Britta Kluge, et al.
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