Discovery of rare ancestry-specific variants in the fetal genome that confer risk of preterm premature rupture of membranes (PPROM) and preterm birth Article

Modi, Bhavi P, Parikh, Hardik, Teves, Maria E et al. (2018). Discovery of rare ancestry-specific variants in the fetal genome that confer risk of preterm premature rupture of membranes (PPROM) and preterm birth . BMC Medical Genetics, 19 10.1186/s12881-018-0696-4

Open Access

cited authors

  • Modi, Bhavi P; Parikh, Hardik; Teves, Maria E; Kulkarni, Rewa; Liyu, Jiang; Romero, Roberto; York, Timothy P; Strauss, Jerome F

sustainable development goals

authors

publication date

  • October 5, 2018

published in

keywords

  • DISEASE
  • Defensin beta 1
  • GENES
  • Genetics & Heredity
  • IDENTIFICATION
  • Life Sciences & Biomedicine
  • Mannose binding lectin-2
  • Methyltransferase like 7B
  • POLYMORPHISMS
  • PREGNANCY
  • Preterm premature rupture of membranes
  • Science & Technology
  • Whole exome sequencing

Digital Object Identifier (DOI)

volume

  • 19