Add Yahoo as a preferred source to see more of our stories on Google. Gypsy Rose Blanchard revealed that her daughter, Aurora, tested negative for 1q21.1 microdeletion, which is a genetic condition ...

In a recent study published in the Genes journal, researchers assessed the impact of PARK2 duplication or microdeletion on neurological diseases such as Parkinson's. The Parkinson's disease 2 (PARK2) ...

Researchers are closer to solving the puzzle of a complex neurological condition called 15q13.3 microdeletion syndrome. Individuals with this condition are missing a small piece of chromosome 15 that ...

Blanchard was first diagnosed with microdeletion 1Q21.1 in 2012 Gypsy-Rose Blanchard's daughter has not inherited the rare genetic condition that she has. On Wednesday, April 23, the 33-year-old ...

Researchers are closer to solving the puzzle of a complex neurological condition called 15q13.3 microdeletion syndrome. Individuals with this condition are missing a small piece of chromosome 15 that ...

Purpose: The advent of molecular cytogenetic technologies has altered the means by which new microdeletion syndromes are identified. Whereas the cytogenetic basis of microdeletion syndromes has ...

Researchers at Baylor College of Medicine, the Jan and Dan Duncan Neurological Research Institute (Duncan NRI) at Texas Children's Hospital, Baylor Genetics and collaborating institutions provided a ...

Researchers are closer to solving the puzzle of a complex neurological condition called 15q13.3 microdeletion syndrome. Individuals with this condition are missing a small piece of chromosome 15 that ...

Co-authors on a paper in the journal Science reporting a link between a chromosomal microdeletion and spina bifida include (from left) Joseph Gleeson and Keng Ioi “Harry” Vong, both of the UC San ...

A Scottish woman who feels virtually no pain has left British researchers not only astounded but looking for a way to harness her previously unidentified genetic mutation to guide new treatments for a ...