Newborn screening panels aim to identify genetic disorders early in life , allowing for timely intervention and improved health outcomes. The use of genomics in newborn screening can facilitate the detection of a broad range of conditions, enabling more accurate and comprehensive testing. Genet offers services to support the development and implementation of recommended newborn screening panels, helping to advance the field of genetic testing and improve the quality of care for newborns and their families.
Studying mitochondrial disorders, which result from mitochondrial dysfunction, can reveal critical information about the genetic basis of these conditions. By focusing on the genomics aspects of mitochondrial disorders, researchers can work towards early detection, prevention, […]
By studying the genetic aspects of nutritional and metabolic diseases, researchers can gain a deeper understanding of the complex interplay between genes, diet, and metabolism. Genomics research can contribute to early detection, prevention, and the […]
Investigating the genetic factors associated with respiratory tract diseases can provide valuable insights into the development and progression of these conditions affecting the lungs and airways. Genomic research can contribute to early detection, prevention, and […]