Found: 26
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Cystic hygroma and omphalocele at 11 weeks in a fetus with monosomy X.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 381, doi. 10.1002/pd.1409
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- Article
Prenatal diagnosis of autosomal recessive polycystic kidney disease (ARPKD) without DNA from an index patient in a current pregnancy.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 392, doi. 10.1002/pd.1420
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- Article
The relation between fetal nasal bone length and biparietal diameter in the Korean population.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 321, doi. 10.1002/pd.1402
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- Article
Isodicentric Yp: prenatal diagnosis and outcome in 12 cases.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 324, doi. 10.1002/pd.1406
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- Article
Second-trimester prenatal screening for trisomy 21 using biochemical markers: a 7-year experience in one cytogenetic laboratory.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 308, doi. 10.1002/pd.1398
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- Article
Doubtful association between TAR syndrome and increased nuchal translucency in the first trimester of pregnancy.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 382, doi. 10.1002/pd.1413
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- Article
The anuric preterm newborn infant with a normal renal ultrasound: a diagnostic and ethical challenge.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 350, doi. 10.1002/pd.1417
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- Article
Prenatal diagnosis of type II osteogenesis imperfecta, describing a new mutation in the COL1A1 gene.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 394, doi. 10.1002/pd.1428
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- Article
Prenatal phenotypic overlap of Costello syndrome and severe Noonan syndrome by tri-dimensional ultrasonography.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 340, doi. 10.1002/pd.1412
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- Article
Current awareness in prenatal diagnosis.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 395, doi. 10.1002/pd.1329
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- Article
Karyotype and outcome of fetuses diagnosed with cystic hygroma in the first trimester in relation to nuchal translucency thickness.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 369, doi. 10.1002/pd.1423
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- Article
Noninvasive genotyping of 9 Y-chromosome specific STR loci using circulatory fetal DNA in maternal plasma by multiplex PCR.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 362, doi. 10.1002/pd.1422
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- Article
Anencephaly and twins.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 380, doi. 10.1002/pd.1405
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- Article
Prenatal diagnosis of low-level mosaicism for a small XIST-negative supernumerary ring X chromosome in a nondysmorphic male fetus.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 387, doi. 10.1002/pd.1416
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- Article
Does prenatal screening influence anxiety levels of pregnant women? A longitudinal randomised controlled trial.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 354, doi. 10.1002/pd.1419
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- Article
Detecting sex chromosome anomalies and common triploidies in products of conception by array-based comparative genomic hybridization.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 333, doi. 10.1002/pd.1411
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- Article
Prenatal diagnosis of the fetal frontal encephalocele by three-dimensional ultrasound.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 378, doi. 10.1002/pd.1404
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- Article
Fetal enterolithiasis: prenatal sonographic and MRI diagnosis in two cases of urorectal septum malformation (URSM) sequence.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 345, doi. 10.1002/pd.1415
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- Article
Unusual sonographic features of ARPKD.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 330, doi. 10.1002/pd.1410
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- Article
Prenatal ultrasound and MRI predict placental localization in a combined intrauterine and extrauterine twin pregnancy.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 376, doi. 10.1002/pd.1403
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- Article
Prenatal identification of small supernumerary marker chromosomes by FISH in an infant born with mild congenital anomalies.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 383, doi. 10.1002/pd.1414
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- Article
Prenatal diagnosis and management of twin pregnancies complicated by a co-existing molar pregnancy.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 373, doi. 10.1002/pd.1380
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- Article
Anencephaly and twins-reply.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 391, doi. 10.1002/pd.1418
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- Article
Prenatal diagnosis of bronchial atresia, early in pregnancy.
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 373, doi. 10.1002/pd.1395
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- Article
Risk estimates for uniparental disomy following prenatal detection of a nonhomologous Robertsonian translocation.
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- 2006
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- Publication type:
- Other
Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32→qter) and partial monosomy 21q (21q22.2→qter).
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- Prenatal Diagnosis, 2006, v. 26, n. 4, p. 313, doi. 10.1002/pd.1399
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- Article