In addition to the surprising revelation that our chromosomes harbor fewer genes than originally predicted, the Human Genome Project also unveiled that all individuals share approximately 99.9% of ...

Using SNP-CGH to Profile for Amplifications, Duplications, and Deletions The beginnings of personalized medicine have been forged by recent advances in SNP genotyping technologies. It is now possible ...

Expert Rev Proteomics. 2007;4(6):741-756. The combined use of microarrays, CGH and SNP arrays in cancer will probably prove important in uncovering more specific tumor and host prognostic and ...

I appreciate the opportunity to comment on the thoughtful letter by Drs. Saul and Moeschler in response to my recent editorial in the New England Journal of Medicine on new, recurrent microdeletion ...