Newborn whole genome sequencing for genetic disease risk
Part of Genetic & congenital clinical trials.
This study looks at using whole genome sequencing in newborns and families with ongoing pregnancies, including those conceived naturally or with fertility treatments. It aims to better understand and manage genetic disease risks early.
Summary written for real people, not researchers, by Clin2.
Who can take part
- You are a family with an ongoing pregnancy (whether conceived naturally or with fertility treatment).
- You have a newborn infant.
Quick eligibility check
Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.
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