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M Stumm

Showing results (41-50 of 57) with videos related to

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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.
Cancer Genetics and Cytogenetics|November 24, 1999
Partial monosomy 2p as the single chromosomal anomaly in a case of renal metanephric adenomaM Stumm, A Koch, P F Wieacker, 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.
Journal of Medical Genetics|January 3, 2001
Atypical clinical picture of the Nijmegen breakage syndrome associated with developmental abnormalities of the brainK H Chrzanowska, M Stumm, M Bekiesiska-Figatowska, 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 6

Showing results (41-50 of 57) with videos related to

Sort By:
Pageof 6
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.
Cancer Genetics and Cytogenetics|November 24, 1999
Partial monosomy 2p as the single chromosomal anomaly in a case of renal metanephric adenomaM Stumm, A Koch, P F Wieacker, 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.
Journal of Medical Genetics|January 3, 2001
Atypical clinical picture of the Nijmegen breakage syndrome associated with developmental abnormalities of the brainK H Chrzanowska, M Stumm, M Bekiesiska-Figatowska, 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 6