Zahn S - Search Results

1

Further delineation of the phenotype maps for partial trisomy 16q24 and Jacobsen syndrome by a subtle familial translocation t(11;16)(q24.2;q24.1).

Zahn S, Ehrbrecht A, Bosse K, Kalscheuer V, Propping P, Schwanitz G, Albrecht B, Engels H. Zahn S, et al. Am J Med Genet A. 2005 Nov 15;139(1):19-24. doi: 10.1002/ajmg.a.30995. Am J Med Genet A. 2005. PMID: 16222663

2

Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations.

Engels H, Bosse K, Ehrbrecht A, Zahn S, Hoischen A, Propping P, Bindl L, Reutter H. Engels H, et al. Among authors: zahn s. Am J Med Genet. 2002 Aug 1;111(2):205-9. doi: 10.1002/ajmg.10560. Am J Med Genet. 2002. PMID: 12210352 Review.

3

Comprehensive analysis of human subtelomeres with combined binary ratio labelling fluorescence in situ hybridisation.

Engels H, Ehrbrecht A, Zahn S, Bosse K, Vrolijk H, White S, Kalscheuer V, Hoovers JM, Schwanitz G, Propping P, Tanke HJ, Wiegant J, Raap AK. Engels H, et al. Among authors: zahn s. Eur J Hum Genet. 2003 Sep;11(9):643-51. doi: 10.1038/sj.ejhg.5201028. Eur J Hum Genet. 2003. PMID: 12939649

4

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

5

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

6

The CXC-chemokine neutrophil-activating peptide-2 induces two distinct optima of neutrophil chemotaxis by differential interaction with interleukin-8 receptors CXCR-1 and CXCR-2.

Ludwig A, Petersen F, Zahn S, Götze O, Schröder JM, Flad HD, Brandt E. Ludwig A, et al. Among authors: zahn s. Blood. 1997 Dec 1;90(11):4588-97. Blood. 1997. PMID: 9373270 Free article.

7

Imbalances of chromosome arm 1p in pediatric and adult germ cell tumors are caused by true allelic loss: a combined comparative genomic hybridization and microsatellite analysis.

Zahn S, Sievers S, Alemazkour K, Orb S, Harms D, Schulz WA, Calaminus G, Göbel U, Schneider DT. Zahn S, et al. Genes Chromosomes Cancer. 2006 Nov;45(11):995-1006. doi: 10.1002/gcc.20363. Genes Chromosomes Cancer. 2006. PMID: 16897744

8

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

9

Molecular genetic analysis of central nervous system germ cell tumors with comparative genomic hybridization.

Schneider DT, Zahn S, Sievers S, Alemazkour K, Reifenberger G, Wiestler OD, Calaminus G, Göbel U, Perlman EJ. Schneider DT, et al. Among authors: zahn s. Mod Pathol. 2006 Jun;19(6):864-73. doi: 10.1038/modpathol.3800607. Mod Pathol. 2006. PMID: 16607373 Free article.

10

Pathology and molecular biology of teratomas in childhood and adolescence.

Harms D, Zahn S, Göbel U, Schneider DT. Harms D, et al. Among authors: zahn s. Klin Padiatr. 2006 Nov-Dec;218(6):296-302. doi: 10.1055/s-2006-942271. Klin Padiatr. 2006. PMID: 17080330

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