Publications by authors named "Susanne Zahn"

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Analysis of the adenomatous polyposis coli (APC) gene in childhood and adolescent germ cell tumors.
Vera Okpanyi, Dominik T Schneider, Susanne Zahn, Sonja Sievers, Gabriele Calaminus

Pediatr Blood Cancer· March 2011

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Hypermethylation of the APC promoter but lack of APC mutations in myxoid/round-cell liposarcoma.
Sonja Sievers, Carla Fritzsch, Marcus Lehnhardt, Susanne Zahn, Nadine Kutzner

Int J Cancer· November 2006

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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.
Susanne Zahn, Sonja Sievers, Katayoun Alemazkour, Sandra Orb, Dieter Harms

Genes Chromosomes Cancer· November 2006

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Constitutive activation of neuregulin/ERBB3 signaling pathway in clear cell sarcoma of soft tissue.
Karl-Ludwig Schaefer, Kristin Brachwitz, Yvonne Braun, Raihanatou Diallo, Daniel H Wai, Susanne Zahn

Neoplasia· July 2006

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Molecular genetic analysis of central nervous system germ cell tumors with comparative genomic hybridization.
Dominik T Schneider, Susanne Zahn, Sonja Sievers, Katayoun Alemazkour, Guido Reifenberger

Mod Pathol· June 2006

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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.
Sonja Sievers, Katayoun Alemazkour, Susanne Zahn, Elizabeth J Perlman, Ad J M Gillis

Genes Chromosomes Cancer· November 2005

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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).
Susanne Zahn, Antje Ehrbrecht, Kristin Bosse, Vera Kalscheuer, Peter Propping

Am J Med Genet A· November 2005

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Identification of recurrent chromosomal aberrations in germ cell tumors of neonates and infants using genomewide array-based comparative genomic hybridization.
Imke Veltman, Joris Veltman, Irene Janssen, Christina Hulsbergen-van de Kaa, Wolter Oosterhuis, Susanne Zahn

Genes Chromosomes Cancer· August 2005

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Comprehensive analysis of human subtelomeres with combined binary ratio labelling fluorescence in situ hybridisation.
Hartmut Engels, Antje Ehrbrecht, Susanne Zahn, Kristin Bosse, Hans Vrolijk

Eur J Hum Genet· September 2003

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Homozygous mutations in caveolin-3 cause a severe form of rippling muscle disease.
Christian Kubisch, Benedikt G H Schoser, Monika von Düring, Regina C Betz, Hans-Hilmar Goebel, Susanne Zahn

Ann Neurol· April 2003

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Further case of Cantú syndrome: exclusion of cryptic subtelomeric chromosome aberrations.
Hartmut Engels, Kristin Bosse, Antje Ehrbrecht, Susanne Zahn, Alexander Hoischen

Am J Med Genet· August 2002

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