A newborn genomic screening test that detects major genetic diseases and chromosomal abnormalities including Wilson disease, ADHD, and hearing loss. This test serves as the first essential health screening for newborns.
Manufactured by
Eone-Diagnomics Genome Center
South Korea
Global NGS Company, EDGCWe provide the value for a healthy lifestyle by suggesting customized healthcare based on genome information.Through genome analysis, we have provided genetic screening tests to help people predict cancer and diseases and to offer personalized healthcare.We have developed cutting-edge diagnostic solutions that empower individuals to make informed health decisions.
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STRATEC/Diatron · Germany
Diagnostic test for identifying genetic disorders through molecular analysis of biological samples. The test can detect chromosomal abnormalities and inherited genetic conditions.
Origin Biotechnology Co., Ltd. · Taiwan
A molecular medicine-based screening test for prenatal diagnosis and prevention of genetic abnormalities. The test provides rapid results to support clinical decision-making in maternal-fetal medicine.
Singlera GENOMICS (SHANGHAI) Ltd. · China
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