Pages that link to "Q57306568"
The following pages link to The BabySeq project: implementing genomic sequencing in newborns (Q57306568):
Displaying 12 items.
- Parental interest in genomic sequencing of newborns: enrollment experience from the BabySeq Project (Q57157559) (← links)
- Perceived Benefits, Risks, and Utility of Newborn Genomic Sequencing in the BabySeq Project (Q63446436) (← links)
- Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project (Q63614921) (← links)
- Recent developments in genetic/genomic medicine (Q64061836) (← links)
- Predispositional genome sequencing in healthy adults: design, participant characteristics, and early outcomes of the PeopleSeq Consortium (Q64095266) (← links)
- What Results Should Be Returned from Opportunistic Screening in Translational Research? (Q89978241) (← links)
- Geographic and Specialty Access Disparities in US Pediatric Leukodystrophy Diagnosis (Q90116249) (← links)
- Considerations for clinical curation, classification, and reporting of low-penetrance and low effect size variants associated with disease risk (Q92419715) (← links)
- Infant mortality: the contribution of genetic disorders (Q92509662) (← links)
- Personalized Medicine and the Power of Electronic Health Records (Q92555536) (← links)
- Exome sequencing in newborns with congenital deafness as a model for genomic newborn screening: the Baby Beyond Hearing project (Q92890307) (← links)
- Targeted next generation sequencing for newborn screening of Menkes disease (Q97885766) (← links)