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Homozygous mutations in caveolin-3 cause a severe form of rippling muscle disease.
Kubisch C, Schoser BG, von Düring M, Betz RC, Goebel HH, Zahn S, Ehrbrecht A, Aasly J, Schroers A, Popovic N, Lochmüller H, Schröder JM, Brüning T, Malin JP, Fricke B, Meinck HM, Torbergsen T, Engels H, Voss B, Vorgerd M. Kubisch C, et al. Among authors: zahn s. Ann Neurol. 2003 Apr;53(4):512-20. doi: 10.1002/ana.10501. Ann Neurol. 2003. PMID: 12666119
Identification of recurrent chromosomal aberrations in germ cell tumors of neonates and infants using genomewide array-based comparative genomic hybridization.
Veltman I, Veltman J, Janssen I, Hulsbergen-van de Kaa C, Oosterhuis W, Schneider D, Stoop H, Gillis A, Zahn S, Looijenga L, Göbel U, van Kessel AG. Veltman I, et al. Among authors: zahn s. Genes Chromosomes Cancer. 2005 Aug;43(4):367-76. doi: 10.1002/gcc.20208. Genes Chromosomes Cancer. 2005. PMID: 15880464
Molecular genetic analysis of bilateral ovarian germ cell tumors.
Hennes E, Zahn S, Lopes LF, Schönberger S, Leuschner I, Göbel U, Calaminus G, Schneider DT. Hennes E, et al. Among authors: zahn s. Klin Padiatr. 2012 Oct;224(6):359-65. doi: 10.1055/s-0032-1327606. Epub 2012 Nov 9. Klin Padiatr. 2012. PMID: 23143763
IGF2/H19 imprinting analysis of human germ cell tumors (GCTs) using the methylation-sensitive single-nucleotide primer extension method reflects the origin of GCTs in different stages of primordial germ cell development.
Sievers S, Alemazkour K, Zahn S, Perlman EJ, Gillis AJ, Looijenga LH, Göbel U, Schneider DT. Sievers S, et al. Among authors: zahn s. Genes Chromosomes Cancer. 2005 Nov;44(3):256-64. doi: 10.1002/gcc.20237. Genes Chromosomes Cancer. 2005. PMID: 16001432
220 results