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 the development of personalized and precision medicine approaches. Genet offers a variety of services to support research in this area, promoting advancements in understanding the genetic factors underlying respiratory tract diseases and enabling the development of targeted therapies.
Genetic Disease Research
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
This page represents genomic investigations available for a diverse array of genetic conditions that affect infants and children from birth or shortly thereafter. By studying the genetics and genomics of these disorders, researchers can identify […]
Genetic Disease Research
Recommended Newborn Screening Panels
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 […]
Genetic Disease Research
Mitochondrial Disorders
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, […]
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