Latest TBX1 Stories
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.
In the United States, a baby is born with a facial cleft every hour, of every day of the year! Such birth defects result from both gene mutations and environmental insults.
Research sheds light on early embryogenesis, genetic disease.
Research sheds light on prenatal heart formation, chromosome 22q.11 deletion syndrome.
--Research Sheds Light on Prenatal Heart Formation, Chromosome 22q.11 Deletion Syndrome-- PHILADELPHIA, May 13 /PRNewswire-USNewswire/ -- Researchers studying the common genetic disorder chromosome 22q.11 deletion syndrome have identified key proteins that act together to regulate early embryonic development.