. . . . . . . "[Placenta slides of 65 IUFDs with known maternal thrombophilia test results (compound MTHFR C677T and A1298C heterozygosity, n?=?10; MTHFR 677TT homozygosity, n?=?3; protein S deficiency, n?=?0; factor V Leiden mutation, n?=?2; prothrombin gene mutation G20210A, n?=?1; lupus anticoagulant, n?=?2; antiphospholipid syndrome, n?=?1; MTHFR C677T heterozygosity, n?=?5; MTHFR A1298C heterozygosity, n?=?4; and MTHFR 1298CC homozygosity, n?=?2) and of 30 livebirths with positive maternal thrombophilia test results (n?=?5, 2, 0, 9, 2, 0, 2, 7, 2 and 1, respectively, for those thrombophilias) were microscopically examined for septation, fetal vessel thrombosis, intimal fibrin cushions, avascular villi, haemorrhagic endovasculitis and fibromuscular sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2017-02-19"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:12:34+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .