Article
Genome sequencing as a first-line diagnostic test for hospitalized newborns
2021-09-11
Abstract excerpt
<h4>ABSTRACT</h4> <h4>Purpose</h4> SouthSeq, a translational research study to perform genome sequencing (GS) for infants with symptoms suggestive of a genetic disorder, was conducted in NICUs in the Southeastern US. Recruitment targeted racial/ethnic minorities and rural, medically underserved areas that are historically under-represented in genomic medicine research. <h4>Methods</h4> GS and analysis were perform...
Topics
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- Ethics and Legal Issues in Pediatric Healthcare
- Genetic factors in colorectal cancer
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Metabolism and Genetic Disorders
- Neonatal Respiratory Health Research
- Neurogenetic and Muscular Disorders Research
Identifiers and source
- Literature Corpus work
- ba6adb23-0ca8-5704-864f-652141da64d8
- DOI
- 10.1101/2021.08.31.21262633
