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1 One baby was stillborn.
2 re affected, 2 (22%) unaffected, and 3 (33%) stillborn.
3 Thirty-nine babies were born healthy, 1 was stillborn, 2 were small for gestational age, 1 had trans
5 ads to perinatal lethality: mutant mice were stillborn and many of them died in utero before birth (b
6 n was found between the risk of a baby being stillborn and the father's total exposure to external io
8 d 9.6 times, respectively, more likely to be stillborn and were 6.4 and 36.7 times, respectively, mor
10 ed in a live birth, two preterm infants were stillborn, and four pregnancies resulted in early sponta
13 circumstances has twice the risk of having a stillborn child when compared to her more advantaged cou
17 ain reaction (PCR) both patients delivered a stillborn fetus with persistent EVD-PCR amniotic fluid p
18 olled residents with deliveries of 1 or more stillborn fetuses and a representative sample of deliver
19 e assayed for mutations in these genes in 33 stillborn fetuses that had bilateral or unilateral renal
21 certainty range 2.4-3.0 million) babies were stillborn, giving a 19% decline in numbers since 2000 wi
23 oat swabs, and brain tissue from aborted and stillborn human fetuses, as well as from horse brain tis
27 on variables included seeing and holding the stillborn infant, having a funeral, and keeping mementoe
28 ts were compared with age-matched infants or stillborn infants ("early" and "late" control subjects).
31 mates appeared biased when only liveborn and stillborn infants were included among cases compared wit
32 stochemistry was performed on placentas from stillborn infants whose cause of death was recorded as V
33 Compared with women who delivered liveborn/stillborn infants with an NTD, women who electively term
38 g fetuses and infants electively terminated, stillborn, or born alive) and with mothers of 539 nonmal
40 f inheritance with 100% penetrance, with the stillborns representing lethal homozygotes that died in
41 r, and 1 had fetal death, with the macerated stillborn showing diffuse cutaneous maculopapillary skin
43 The phenotype in CDPX2 females ranges from stillborn to mildly affected individuals identified in a
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