CPT under-specification for molecular diagnostics promotes widespread use of unclassified codes, undermining payer coverage ...
Morning Overview on MSN
A genetic disorder tied to autism turns out to affect 1 in 7,300 people
Phelan-McDermid syndrome, a rare genetic disorder in which many patients also have autism, may affect about 1 in 7,300 people ...
The recent update to fair value, from US$3.37 to US$3.91 per share for Myriad Genetics, reflects a recalibration of what ...
Channel Lab founder David Navrátil is building Genome X, a Czech genetic lab that aims to replace averaged treatment plans ...
New guidance co-led by University of Otago researchers could help more people with suspected inherited diseases receive a ...
Japanese researchers used CRISPR-Cas9 to remove the extra chromosome 21 from cells in a lab. It’s a real breakthrough — but ...
Rare genetic diseases can go years, or even decades, without diagnosis. Standard testing often misdiagnoses these diseases, ...
Susan Dymecki, the George Fabyan Professor of Genetics in the Field of Comparative Pathology in the Blavatnik Institute at ...
Morning Overview on MSN
One gene deletion explains a blood type that stumped labs for 50 years
More than 99.9% of people carry an antigen called AnWj on their red blood cells, and for decades the handful who lacked it were a puzzle that no reference laboratory could close. Scientists at NHS ...
A bad apple doesn't always ruin the bunch. In fact, it might make the bunch a little stronger. A new study published in ...
A ‘ghost’ lobster so rare that the odds of finding it are 1 in 100 million is going to school—a new home at Maine’s Marine ...
A lab at the University of Kentucky Martin-Gatton College of Agriculture, Food and Environment (CAFE) is at the forefront of ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results