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European Journal of Pediatrics|October 5, 2001
Short stature homeobox-containing gene deletion screening by fluorescence in situ hybridisation in patients with short statureJ Musebeck, K Mohnike, P Beye, et al.Prenatal Diagnosis|October 20, 2000
Incidental prenatal detection of an Xp deletion using an anonymous primer pair for fetal sexingS Jakubiczka, B Mitulla, T Liehr, et al.Clinical Genetics|May 1, 1997
Linkage studies exclude the AT-V gene(s) from the translocation breakpoints in an AT-V patientK Chrzanowska, M Stumm, M Bialecka, et al.Prenatal Diagnosis|October 7, 2010
A mixture model of nuchal translucency thickness in screening for chromosomal defects: validation of a single operator datasetA Gasiorek-Wiens, S Kotsis, I Staboulidou, et al.Human Genetics|November 1, 1995
DNA, FISH and complementation studies in ICF syndrome: DNA hypomethylation of repetitive and single copy loci and evidence for a trans acting factorS Schuffenhauer, O Bartsch, M Stumm, et al.American Journal of Human Genetics|March 1, 1997
The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21K Saar, K H Chrzanowska, M Stumm, et al.Ernst Schering Foundation Symposium Proceedings|September 25, 2008
Minimally invasive biomarkers for therapy monitoringP McSheehy, P Allegrini, S Ametaby, et al.Proceedings of the National Academy of Sciences of the United States of America|February 27, 2003
Nonhomologous end joining and V(D)J recombination require an additional factorY Dai, B Kysela, L A Hanakahi, et al.Cancer Research|September 15, 2000
Radiosensitivity in Nijmegen Breakage Syndrome cells is attributable to a repair defect and not cell cycle checkpoint defectsP M Girard, N Foray, M Stumm, et al.Genomics|May 18, 1999
The presynaptic cytomatrix protein Bassoon: sequence and chromosomal localization of the human BSN geneC Winter, S tom Dieck, T M Boeckers, et al.Pageof 9