Genome :: First individual genome sequence published

Independent sequence and assembly of the six billion base pairs from the genome of one person ushers in the era of individualized genomics. Researchers at the J. Craig Venter Institute (JCVI), along with collaborators at The Hospital for Sick Children in Toronto and the University of California San Diego (UCSD), have published a genome sequence of an individual, Craig Venter, that covers both sets of chromosomes that were inherited from each parent.

Genome :: Genome study shines light on genetic link to height

Using a new “genome-scanning” method, a team of scientists has identified the first robust link between genes and stature in humans. A single letter change in a gene called HMGA2 enables people who carry it to gain as much as a centimeter in height. The work provides insights into how genes hardwire growth in humans and suggests that finding additional height-related genes may be feasible.

Childbirth :: Birth Center Medical Team Learns from Special Deliveries

Noelle experienced labor and delivery several times on August 27 and 28, but not because she was expecting triplets. A computerized maternal and neonatal birthing simulator, this NOELLE TMis helping hospital staff at Strong Memorial Hospital of the University of Rochester Medical Center prepare to provide optimal care for mothers and their newborns during childbirth.

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