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Environmental and Molecular Mutagenesis|January 29, 2002
Use of inverse PCR to amplify and sequence breakpoints of HPRT deletion and translocation mutationsM Williams, I R Rainville, J A NicklasSomatic Cell and Molecular Genetics|September 1, 1995
Breakpoints and junctional regions of intragenic deletions in the HPRT gene in human T-CellsI R Rainville, R J Albertini, J A NicklasMutagenesis|May 1, 1997
Large deletions partially external to the human hprt gene result in chimeric transcriptsM J Lippert, I R Rainville, J A Nicklas, et al.Mutation Research|September 3, 1998
Development of long PCR techniques to analyze deletion mutations of the human hprt geneB Van Houten, Y Chen, J A Nicklas, et al.Thrombosis and Haemostasis|October 1, 1994
Homozygous type I protein C deficiency in two unrelated families exhibiting thrombophilia related to Ala136-->Pro or Arg286-->His mutationsG L Long, J A Tomczak, I R Rainville, et al.Blood|March 15, 1992
Protein CVermont: symptomatic type II protein C deficiency associated with two GLA domain mutationsE G Bovill, J A Tomczak, B Grant, et al.Pageof 1