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Audiology & Neuro-Otology|March 18, 2010
GJB2 mutations and genotype-phenotype correlation in 335 patients from germany with nonsyndromic sensorineural hearing loss: evidence for additional recessive mutations not detected by current methodsO Bartsch, A Vatter, U Zechner, et al.
European Journal of Neurology|May 25, 2010
Evaluating the effect of spastin splice mutations by quantitative allele-specific expression assayS Klimpe, A Zibat, U Zechner, et al.
Cytogenetic and Genome Research|December 28, 2007
Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosisO Bartsch, Z Vlcková, F Erdogan, et al.
Molecular Syndromology|January 18, 2013
Novel VANGL1 Gene Mutations in 144 Slovakian, Romanian and German Patients with Neural Tube DefectsO Bartsch, I Kirmes, A Thiede, et al.
Genomics|January 8, 1999
Characterization of the mouse Src homology 3 domain gene Sh3d2c on Chr 7 demonstrates coexpression with huntingtin in the brain and identifies the processed pseudogene Sh3d2c-ps1 on Chr 2U Zechner, S Scheel, M Hemberger, et al.
Human Molecular Genetics|December 1, 1994
A YAC clone map spanning 7.5 megabases of human chromosome band Xq28U C Rogner, P Kioschis, K Wilke, et al.
Journal of Physiology and Pharmacology : an Official Journal of the Polish Physiological Society|May 1, 2014
Social isolation-induced epigenetic changes in midbrain of adult miceD Siuda, Z Wu, Y Chen, et al.
Genetics|January 5, 2001
Genetic and developmental analysis of X-inactivation in interspecific hybrid mice suggests a role for the Y chromosome in placental dysplasiaM Hemberger, H Kurz, A Orth, et al.
Oncogene|August 1, 1996
Isolation and characterization of the mouse homolog of SYT, a gene implicated in the development of human synovial sarcomasD R de Bruijn, E Baats, U Zechner, et al.
Genomics|June 6, 1998
An evolutionarily conserved gene on human chromosome 5q33-q34, UBH1, encodes a novel deubiquitinating enzymeT E Hansen-Hagge, J W Janssen, H Hameister, et al.
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