Early access via large-scale clinical study to establish the validity and utility of the FirstGene TM screen ...

Epigenetic changes do not alter the genetic code itself, but by changing how DNA is organized within the cell, epigenetic ...

It ensures that each new generation will include individuals with different gene combinations compared ... risk of congenital disorders such as Down syndrome, in which a child is born with an extra ...

Down syndrome is the most frequent genetic condition and the first chromosomal disorder for which the cause was identified: the presence of 3 copies of all or part of chromosome 21 (Hsa21 ... with a ...

Down Syndrome is a genetic condition caused by the presence of an extra copy of chromosome 21. It leads to developmental variations and characteristics that are unique to individuals with the ...

The café’s name references Trisomy 21, the medical term describing the extra copy of chromosome 21 that causes Down Syndrome. Raghu Raman, Owner and Managing Director of 21 Café, established the venue ...

Mosaic Down syndrome is a variant of Down syndrome. Down syndrome is a congenital (present at birth) genetic condition that occurs when a person has three copies of chromosome 21 instead of two (the ...

“It’s not just about fixing one gene,” explains Dr Oyieke. “Down Syndrome affects 326 genes on chromosome 21—editing that entire package is a monumental challenge.” Ethical concerns ...

Down syndrome is a common chromosomal disorder caused by an extra chromosome 21, leading to intellectual disabilities and distinct physical traits. Early diagnosis and therapies significantly ...