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Genes, Chromosomes & Cancer|August 3, 2004
Spontaneously immortalized human T lymphocytes develop gain of chromosomal region 2p13-24 as an early and common genetic eventJan Konrad Siwicki, Mattias Berglund, Jolanta Rygier, et al.Genes, Chromosomes & Cancer|May 15, 2002
Amplification of the telomerase reverse transcriptase (hTERT) gene in cervical carcinomasAnju Zhang, Chengyun Zheng, Mi Hou, et al.British Journal of Haematology|May 20, 2003
Cytogenetic abnormalities in childhood acute myeloid leukaemia: a Nordic series comprising all children enrolled in the NOPHO-93-AML trial between 1993 and 2001Erik Forestier, Sverre Heim, Elisabeth Blennow, et al.Journal of Medical Genetics|May 3, 2013
A novel intellectual disability syndrome caused by GPI anchor deficiency due to homozygous mutations in PIGTMalin Kvarnung, Daniel Nilsson, Anna Lindstrand, et al.Genes, Chromosomes & Cancer|February 8, 2007
Cytogenetic patterns in ETV6/RUNX1-positive pediatric B-cell precursor acute lymphoblastic leukemia: A Nordic series of 245 cases and review of the literatureErik Forestier, Mette K Andersen, Kirsi Autio, et al.British Journal of Haematology|February 5, 2008
Outcome of ETV6/RUNX1-positive childhood acute lymphoblastic leukaemia in the NOPHO-ALL-1992 protocol: frequent late relapses but good overall survivalErik Forestier, Mats Heyman, Mette K Andersen, et al.Genes, Chromosomes & Cancer|June 17, 2009
Clinical and cytogenetic features of a population-based consecutive series of 285 pediatric T-cell acute lymphoblastic leukemias: rare T-cell receptor gene rearrangements are associated with poor outcomeKristina Karrman, Erik Forestier, Mats Heyman, et al.Nature Communications|January 28, 2014
Clonal culturing of human embryonic stem cells on laminin-521/E-cadherin matrix in defined and xeno-free environmentSergey Rodin, Liselotte Antonsson, Colin Niaudet, et al.Human Molecular Genetics|November 22, 2002
A full-coverage, high-resolution human chromosome 22 genomic microarray for clinical and research applicationsPatrick G Buckley, Kiran K Mantripragada, Magdalena Benetkiewicz, et al.European Journal of Human Genetics : EJHG|September 16, 2004
An excess of chromosome 1 breakpoints in male infertilityIben Bache, Elvire Van Assche, Sultan Cingoz, et al.Pageof 4