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Human Genetics|June 29, 2005
A systematic analysis of LINE-1 endonuclease-dependent retrotranspositional events causing human genetic diseaseJian-Min Chen, Peter D Stenson, David N Cooper, et al.
Human Mutation|January 12, 2005
Meta-analysis of gross insertions causing human genetic disease: novel mutational mechanisms and the role of replication slippageJian-Min Chen, Nadia Chuzhanova, Peter D Stenson, et al.
Human Mutation|August 20, 2005
Intrachromosomal serial replication slippage in trans gives rise to diverse genomic rearrangements involving inversionsJian-Min Chen, Nadia Chuzhanova, Peter D Stenson, et al.
Nature Reviews. Genetics|September 12, 2007
Gene conversion: mechanisms, evolution and human diseaseJian-Min Chen, David N Cooper, Nadia Chuzhanova, et al.
Human Mutation|June 25, 2005
Complex gene rearrangements caused by serial replication slippageJian-Min Chen, Nadia Chuzhanova, Peter D Stenson, et al.
American Journal of Human Genetics|September 12, 2024
Alu insertion-mediated dsRNA structure formation with pre-existing Alu elements as a disease-causing mechanismEmmanuelle Masson, Sandrine Maestri, Valérie Bordeau, et al.
Seminars in Cancer Biology|June 15, 2010
Genomic rearrangements in inherited disease and cancerJian-Min Chen, David N Cooper, Claude Férec, et al.
Genes|November 18, 2020
Role of the Common <i>PRSS1-PRSS2</i> Haplotype in Alcoholic and Non-Alcoholic Chronic Pancreatitis: Meta- and Re-AnalysesAnthony F Herzig, Emmanuelle Génin, David N Cooper, et al.
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