HIGHLIGHTS
- who: Alexandra Emms and collaborators from the Birmingham , TG, UK University of Birmingham, Birmingham , TT, UK have published the research: Next Generation Sequencing after Invasive Prenatal Testing in Fetuses with Congenital Malformations: Prenatal or Neonatal Investigation, in the Journal: Genes 2022, 13, 1517. of /2022/
- what: Next generation sequencing is increasingly used for the diagnosis of monogenic disorders in fetuses with structural congenital abnormalities, as demonstrated by the R21 pathway in the NHS in England, as part of postnatal investigation of the sick neonate via the R14 pathway, and in the R27 and R412 pathways . . .
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