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K Wimmer

Showing results (21-30 of 70) with videos related to

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Clinical Genetics|May 16, 2017
Constitutional mismatch repair deficiency in a healthy child: On the spot diagnosis?M Suerink, T P Potjer, A B Versluijs, et al.
British Journal of Haematology|September 6, 2000
Mapping of leukaemia-associated breakpoints in chromosome band 3q21 using a newly established PAC contigR Wieser, A Volz, S Schnittger, et al.
European Journal of Medical Genetics|August 12, 2009
Two sporadic spinal neurofibromatosis patients with malignant peripheral nerve sheath tumourC Fauth, H Kehrer-Sawatzki, A Zatkova, et al.
Dento Maxillo Facial Radiology|May 31, 2007
Intraorbital plexiform neurofibroma in an NF-1-negative patientS Jank, E J Raubenheimer, M R Bouckaert, et al.
Genomics|December 1, 1996
Two-dimensional separation and cloning of chromosome 1 NotI-EcoRV-derived genomic fragmentsK Wimmer, D Thoraval, J Asakawa, et al.
Human Mutation|February 22, 2007
Extensive in silico analysis of NF1 splicing defects uncovers determinants for splicing outcome upon 5' splice-site disruptionK Wimmer, X Roca, H Beiglböck, et al.
DNA Repair|May 22, 2012
Unique mutational profile associated with a loss of TDG expression in the rectal cancer of a patient with a constitutional PMS2 deficiencyP Vasovcak, A Krepelova, M Menigatti, et al.
Annals of Surgical Oncology|December 25, 2019
Impact of Surgical Margins in Breast Cancer After Preoperative Systemic Chemotherapy on Local Recurrence and SurvivalK Wimmer, M Bolliger, Z Bago-Horvath, et al.
Medical and Pediatric Oncology|July 24, 2001
Two-dimensional DNA electrophoresis identifies novel CpG islands frequently coamplified with MYCN in neuroblastomaK Wimmer, X X Zhu, B J Lamb, et al.
American Journal of Human Genetics|July 17, 2004
High frequency of mosaicism among patients with neurofibromatosis type 1 (NF1) with microdeletions caused by somatic recombination of the JJAZ1 geneH Kehrer-Sawatzki, L Kluwe, C Sandig, et al.
Pageof 7

Showing results (21-30 of 70) with videos related to

Sort By:
Pageof 7
Clinical Genetics|May 16, 2017
Constitutional mismatch repair deficiency in a healthy child: On the spot diagnosis?M Suerink, T P Potjer, A B Versluijs, et al.
British Journal of Haematology|September 6, 2000
Mapping of leukaemia-associated breakpoints in chromosome band 3q21 using a newly established PAC contigR Wieser, A Volz, S Schnittger, et al.
European Journal of Medical Genetics|August 12, 2009
Two sporadic spinal neurofibromatosis patients with malignant peripheral nerve sheath tumourC Fauth, H Kehrer-Sawatzki, A Zatkova, et al.
Dento Maxillo Facial Radiology|May 31, 2007
Intraorbital plexiform neurofibroma in an NF-1-negative patientS Jank, E J Raubenheimer, M R Bouckaert, et al.
Genomics|December 1, 1996
Two-dimensional separation and cloning of chromosome 1 NotI-EcoRV-derived genomic fragmentsK Wimmer, D Thoraval, J Asakawa, et al.
Human Mutation|February 22, 2007
Extensive in silico analysis of NF1 splicing defects uncovers determinants for splicing outcome upon 5' splice-site disruptionK Wimmer, X Roca, H Beiglböck, et al.
DNA Repair|May 22, 2012
Unique mutational profile associated with a loss of TDG expression in the rectal cancer of a patient with a constitutional PMS2 deficiencyP Vasovcak, A Krepelova, M Menigatti, et al.
Annals of Surgical Oncology|December 25, 2019
Impact of Surgical Margins in Breast Cancer After Preoperative Systemic Chemotherapy on Local Recurrence and SurvivalK Wimmer, M Bolliger, Z Bago-Horvath, et al.
Medical and Pediatric Oncology|July 24, 2001
Two-dimensional DNA electrophoresis identifies novel CpG islands frequently coamplified with MYCN in neuroblastomaK Wimmer, X X Zhu, B J Lamb, et al.
American Journal of Human Genetics|July 17, 2004
High frequency of mosaicism among patients with neurofibromatosis type 1 (NF1) with microdeletions caused by somatic recombination of the JJAZ1 geneH Kehrer-Sawatzki, L Kluwe, C Sandig, et al.
Pageof 7