Discovery of rare ancestry-specific variants in the fetal genome that confer risk of preterm premature rupture of membranes (PPROM) and preterm birth
Crossref DOI link:
Update policy: https://doi.org/10.1007/SPRINGER_CROSSMARK_POLICY
Modi, Bhavi P.
Parikh, Hardik I.
Teves, Maria E.
York, Timothy P.
Strauss, Jerome F.
Funding for this research was provided by:
Burroughs Wellcome Fund (#1015040)
National Institutes of Health (R01 HD073555)
Eunice Kennedy Shriver National Institute of Child Health and Human Development (HSN275201300006C)