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Neonatal outcome of a prenatally detected 46,XX/46,XY true hermaphrodite.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 185, doi. 10.1002/pd.1371
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- Article
Prenatal diagnosis of congenital epulis by three-dimensional ultrasound and magnetic resonance imaging.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 171, doi. 10.1002/pd.1368
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Favourable outcome in a pregnancy with concomitant maternal and fetal osteogenesis imperfecta associated with a novel COL1A2 mutation.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 188, doi. 10.1002/pd.1375
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Natural history of prenatally diagnosed 46,X,isodicentric Y.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 134, doi. 10.1002/pd.1352
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The fetal mandible: an in utero sonographic evaluation between 11 and 31 weeks' gestation.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 163, doi. 10.1002/pd.1363
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Fetal paroxysmal supraventricular tachycardia without heart failure leading to ischemic damage.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 187, doi. 10.1002/pd.1374
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Ultrasonographic evaluation of fetal nasal bone in a low-risk population at 11-13 + 6 gestational weeks.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 112, doi. 10.1002/pd.1345
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Prenatal diagnosis of pure distal 18q deletion.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 184, doi. 10.1002/pd.1367
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Current awareness in prenatal diagnosis.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 195, doi. 10.1002/pd.1327
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- Article
Postmortem evaluation of 220 prenatally diagnosed fetuses with neural tube defects: detection of associated anomalies in a Turkish population.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 147, doi. 10.1002/pd.1378
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Forty-eight-hour first-trimester glucose profiles in women with type 1 diabetes mellitus: a report of three cases of congenital malformation.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 123, doi. 10.1002/pd.1340
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Maternal serum alpha-fetoprotein, fetal middle cerebral artery blood flow velocity and fetal haemoglobin in pregnancies at risk of fetal anaemia.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 101, doi. 10.1002/pd.1351
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Mid-facial anthropometry in second-trimester fetuses with trisomy 21: a three-dimensional ultrasound study.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 158, doi. 10.1002/pd.1362
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Evidence of genetic underexpression in chorionic villi samples of euploid fetuses with increased nuchal translucency at 10-11 weeks' gestation.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 128, doi. 10.1002/pd.1373
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Women's opinions on the offer and use of nuchal translucency screening for Down syndrome.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 105, doi. 10.1002/pd.1344
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Detection of maternal deoxyribonucleic acid in peripheral blood of premature and mature newborn infants.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 168, doi. 10.1002/pd.1366
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Bilateral fetal hyperechogenic kidneys associated with normal amniotic fluid: an ethical dilemma in a normal variant?
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 190, doi. 10.1002/pd.1377
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Amniocentesis for karyotyping prior to induction of abortion at second trimester.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 192, doi. 10.1002/pd.1388
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Fetal microchimerism is not involved in the pathogenesis of lichen sclerosus of the vulva.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 175, doi. 10.1002/pd.1372
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Prenatal diagnosis of an exceptional intrauterine herpes simplex type 1 infection.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 154, doi. 10.1002/pd.1361
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Molecular cytogenetic analysis of de novo dup(5)(q33.1q31.1) associated with abnormal perinatal findings.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 181, doi. 10.1002/pd.1365
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Homozygous α-thalassemia associated with micropenis in a fetus.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 180, doi. 10.1002/pd.1343
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Prenatal diagnosis of de novo t(2;18;14)(q33.1;q12.2;q31.2), dup(5)(q34q34), del(7)(p21.1p21.1), and del(10)(q25.3q25.3) and a review of the prenatally ascertained de novo apparently balanced complex and multiple chromosomal rearrangements.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 138, doi. 10.1002/pd.1369
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Umbilical cord pseudocyst in a fetus with Down syndrome.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 193, doi. 10.1002/pd.1376
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De novo chromosomal abnormalities and month of conception.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 118, doi. 10.1002/pd.1358
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Mirror syndrome due to parvovirus B19 hydrops complicated by severe maternal pulmonary effusion.
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- Prenatal Diagnosis, 2006, v. 26, n. 2, p. 179, doi. 10.1002/pd.1342
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