Galetzka, D; Weis, E; Kohlschmidt, N et al.
Expression of somatic DNA repair genes in human testesJ Cell Biochem. Bd. 100. 2007 S. 1232-1239
Nanda, I; Buwe, A; Wizenman, A et al.
Fanconi anemia genes in vertebrates: evolutionary conservation, sex-linkage, and embryonic expression of FANCC and FANCG in avian cellsSchindler D, Hoehn H (Hrsg). Fanconi Anemia. A Paradigmatic Disease for the Understanding of Cancer and Aging. Basel: Karger 2007
Nolte, J; Rathsack, K; Drusenheimer, N et al.
Männliche Keimzellen aus embryonalen StammzellenMedizinische Genetik. Bd. 19. 2007 S. 10-17
Ruf, N; Bähring, S; Galetzka, D et al.
Sequence-based bioinformatic prediction and QUASEP identify genomic imprinting of the KCNK9 potassium channel gene in mouse and humanHum Mol Genet. Bd. 16. 2007 S. 2591-2599
Galetzka, D; Weis, E; Tralau, T et al.
Sex-specific windows for high mRNA expression of DNA methyltransferases 1 and 3A and methyl-CpG-binding domain proteins 2 and 4 in human fetal gonadsMol Reprod Dev. Bd. 74. 2007 S. 233-241
Bartsch, O; Vlckova, Z; Erdogan, F et al.
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 neurofibromatosis.Cytogenet Genome Res. Bd. 119. H. 1-2. 2007 S. 158-64
Mikelsaar, R; Molder, H; Bartsch, O et al.
Two novel deletions (array CGH findings) in pigment dispersion syndrome.Ophthalmic Genet. Bd. 28. H. 4. 2007 S. 216-9
Yue, Y; Haaf, T
7E olfactory receptor gene clusters and evolutionary chromosome rearrangementsCytogenet Genome Res. Bd. 112. 2006 S. 6-10
Metzler, M; Forster, A; Pannell, R et al.
A conditional model of MLL-AF4 B-cell tumourigenesis using invertor technology.Oncogene. Bd. 25. H. 22. 2006 S. 3093-103
Weimer, J; Metzke-Heidemann, S; Plendl, H et al.
Characterization of two supernumerary marker chromosomes in a patient with signs of Klinefelter syndrome, mild facial anomalies, and severe speech delay.Am J Med Genet. Bd. 140. H. 5. 2006 S. 488-95