Non-invasive prenatal testing (NIPT) can help us determine fetal RhD status without a drop of fetal...
Staffing requirements
Thalassemia is typically caused by sequence variants in the HBA1, HBA2 or HBB genes. The common...
Swedish molecular diagnostics company Devyser, announced today at the 45th annual European Bone...
Thalassemia is an inherited blood disorder with a worldwide prevalence of nearly 300,000 per year....
Every year world thrombosis day is held on October 13 to bring awareness to the potential risks of...
Alpha- and beta-thalassemia are distinct hematologic disorders caused by a defect in globin chain...
Chimerism monitoring after hematopoietic stem cell transplantation (HSCT) plays a key role in...
Learnings from our IVDR journey
A recent paper published by Malan et al in the Journal of the American Medical Association (JAMA)...
An expert consensus panel has recently promoted genetic testing for Familial Hypercholesterolemia...
Cystic fibrosis is one of the most common genetic disorders. The disease is caused by mutations...
