New Gene Screening Test To Help Doctors Identify Rare Genetic Diseases In Newborns The next generation of genetic sequencing could pave the way for the speedy molecular diagnosis of rare genetic diseases in newborns. The pilot study conducted by Canadian researchers diagnosed a number of rare conditions in the babies. by Katrina Pascual
Science PacBio's SMRT Sequencing Could Open Secrets Of Gorilla Genome And Human Disease by James Maynard
Healthy Living/Wellness Bravery Genes In Chickens May Shed Light On Anxiety In Humans by Alyssa Navarro