Showing results (21-30 of 181) with videos related to

Sort By:
Pageof 19
Cancer Genetics and Cytogenetics|July 10, 2003
Intratumoral genomic heterogeneity in advanced head and neck cancer detected by comparative genomic hybridizationSusanne C Tremmel, Karl Götte, Susanne Popp, et al.
BMC Bioinformatics|January 29, 2003
Computer aided analysis of additional chromosome aberrations in Philadelphia chromosome positive acute lymphoblastic leukaemia using a simplified computer readable cytogenetic notationJutta Bradtke, Harald Balz, Christa Fonatsch, et al.
European Journal of Medical Genetics|January 8, 2011
3.7 Mb tandem microduplication in chromosome 5p13.1-p13.2 associated with developmental delay, macrocephaly, obesity, and lymphedema. Further characterization of the dup(5p13) syndromeKonrad Oexle, Maja Hempel, Anna Jauch, et al.
Cancers|May 28, 2020
Can 18F-NaF PET/CT before Autologous Stem Cell Transplantation Predict Survival in Multiple Myeloma?Christos Sachpekidis, Annette Kopp-Schneider, Maximilian Merz, et al.
American Journal of Medical Genetics. Part A|July 14, 2006
Trisomy 8q and partial trisomy 22 in a 43-year-old man with moderate intellectual disability, epilepsy and large cell non-Hodgkin lymphomaIngo Helbig, Michael Wirtenberger, Anna Jauch, et al.
Pediatric Nephrology (Berlin, Germany)|March 10, 2004
Tuberous sclerosis and polycystic kidney disease in a 3-month-old infantMartin W Laass, Miriam Spiegel, Anna Jauch, et al.
Stem Cell Research|December 17, 2017
Murine transgenic embryonic stem cell lines for the investigation of sinoatrial node-related molecular pathwaysStefanie Schmitteckert, Anne Griesbeck, Simon Sumer, et al.
Leukemia & Lymphoma|October 14, 2016
Hematopoietic stem cells can be separated from leukemic cells in a subgroup of adult acute lymphoblastic leukemia patientsWenwen Wang, Elena Foerner, Eike Buss, et al.
In Vitro Cellular & Developmental Biology. Animal|January 18, 2006
Multicolor karyotype analyses of mouse embryonic stem cellsJianli Guo, Anna Jauch, Holtgreve-Grez Heidi, et al.
Clinical Dysmorphology|July 19, 2003
Multicolor chromosomal bar coding characterizes a de novo interstitial deletion (5)(q33.3q35.2) in a child with multiple congenital malformationsChristiane Schiffer, Susanne Popp, Sharareh Moshir, et al.
Pageof 19