Latest Chromosome 22 Stories
Two new studies have revealed readily-detectable, early-warning signs of neurological impairment.
Research out of the George Washington University (GW), published in the journal Proceedings of the National Academy of Sciences (PNAS), reveals another piece of the puzzle in a genetic developmental disorder that causes behavioral diseases such as autism.
The discovery of a 'switch' that modifies a gene known to be essential for normal heart development could explain variations in the severity of birth defects in children with DiGeorge syndrome.
World-renowned Professionals Connect with Families July 6 – 10th in Orlando to Discuss Cutting-edge Trends & Treatments Matawan, NJ (PRWEB) June 01, 2012
A healthy genome is characterized by 23 pairs of chromosomes, and even a small change in this structure — such as an extra copy of a single chromosome — can lead to severe physical impairment.
Scientists have discovered a genetic cause of extreme thinness for the first time, in a study published today in the journal Nature.
PHILADELPHIA, Aug. 25 /PRNewswire/ -- In celebration of a seminal discovery in cancer biology, Fox Chase Cancer Center will host the Philadelphia Chromosome Symposium: Past, Present and Future, on September 28, 2010, from 8 a.m. to 7 p.m.
PHILADELPHIA, July 29 /PRNewswire-USNewswire/ --A genetics research team based at The Children's Hospital of Philadelphia continues to discover recurrent translocations--places in which two chromosomes exchange pieces of themselves.
Research sheds light on early embryogenesis, genetic disease.
Research sheds light on prenatal heart formation, chromosome 22q.11 deletion syndrome.
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