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IEEE/ACM Transactions on Computational Biology and Bioinformatics|February 5, 2008
Computational problems in perfect phylogeny haplotyping: typing without calling the alleleTamar Barzuza, Jacques S Beckmann, Ron Shamir, et al.
Drug News & Perspectives|April 5, 2003
Pharmacogenetic Development of Personalized Medicine: Multiple Sclerosis Treatment as a ModelIris Kirstein-Grossman, Jacques S. Beckmann, Doron Lancet, et al.
Human Genomics|April 9, 2005
Trick or treat: the effect of placebo on the power of pharmacogenetic association studiesClara Singer, Iris Grossman, Nili Avidan, et al.
Frontiers in Genetics|June 11, 2013
The Growing Importance of CNVs: New Insights for Detection and Clinical InterpretationArmand Valsesia, Aurélien Macé, Sébastien Jacquemont, et al.
Human Molecular Genetics|July 22, 2008
Two trans-acting eQTLs modulate the penetrance of PRPF31 mutationsThomas Rio Frio, Natacha Civic, Adriana Ransijn, et al.
American Journal of Medical Genetics. Part A|March 9, 2006
Fetus with two identical reciprocal translocations: description of a rare complication of consanguinityDanielle Martinet, Yvan Vial, Francine Thonney, et al.
Molecular and Cellular Biology|March 11, 2009
Transcription factor CTF1 acts as a chromatin domain boundary that shields human telomeric genes from silencingGermain Esnault, Stefano Majocchi, Danielle Martinet, et al.
Psychiatric Genetics|May 21, 2009
Mutation screening of the glutamate cysteine ligase modifier (GCLM) gene in patients with schizophreniaChristophe Butticaz, Thomas Werge, Jacques S Beckmann, et al.
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