Found: 22
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First trimester screening with free β-hCG, PAPP-A and nuchal translucency in pregnancies conceived with assisted reproduction.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 718, doi. 10.1002/pd.390
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- Article
Prenatal diagnosis of female monozygotic twins discordant for Turner syndrome: implications for prenatal genetic counselling.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 697, doi. 10.1002/pd.383
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- Article
Comparison and integration of first trimester fetal nuchal translucency and second trimester maternal serum screening for fetal Down syndrome.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 730, doi. 10.1002/pd.382
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- Article
Female pseudohermaphroditism in a fetus with a deletion 9(q22.2q31.1).
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 652, doi. 10.1002/pd.353
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- Article
Isochromosome 5p mosaicism at prenatal diagnosis: observations and outcomes in six cases at chorionic villus sampling and one at amniocentesis.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 681, doi. 10.1002/pd.379
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- Article
Prenatal identification of esophageal atresia: the role of ultrasonography for evaluation of functional anatomy.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 669, doi. 10.1002/pd.375
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- Article
Is unexplained third trimester intrauterine death of fetuses with gastroschisis caused by umbilical cord compression due to acute extra-abdominal bowel dilatation?
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 715, doi. 10.1002/pd.386
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- Article
Uniparental disomy in fetuses diagnosed with balanced Robertsonian translocations: risk estimate.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 649, doi. 10.1002/pd.370
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- Article
Prenatal diagnosis and intrafamilial clinical heterogeneity of Fraser syndrome.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 692, doi. 10.1002/pd.381
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- Article
Chondrodysplasia punctata (CDP) with features of the tibia-metacarpal type and maternal phenytoin treatment during pregnancy.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 663, doi. 10.1002/pd.352
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- Article
Hypomandibular faciocranial dysostosis in consanguineous parents revealed by ultrasound prenatal diagnosis.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 710, doi. 10.1002/pd.385
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- Article
Novel mutation and prenatal sonographic findings of glutaric aciduria (type I) in two Taiwanese families.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 725, doi. 10.1002/pd.392
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- Article
Current Awareness.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 740, doi. 10.1002/pd.271
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- Article
Maternal cell contamination in an amniotic fluid sample.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 737, doi. 10.1002/pd.378
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- Article
Improved methodology for evaluating nuchal thickness in the second trimester.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 738, doi. 10.1002/pd.389
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- Article
Rapid prenatal diagnosis of sickle cell diseases using oligonucleotide ligation assay coupled with laser-induced capillary fluorescence detection.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 686, doi. 10.1002/pd.380
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- Article
Maternal serum hyperglycosylated human chorionic gonadotrophin (HhCG) in the first trimester of pregnancies affected by Down syndrome, using a sialic acid-specific lectin immunoassay.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 656, doi. 10.1002/pd.351
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- Article
Outcome of prenatally diagnosed trisomy 6 mosaicism.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 722, doi. 10.1002/pd.391
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- Article
Second trimester molecular diagnosis of a stop codon FGFR3 mutation in a type I thanatophoric dysplasia fetus following abnormal ultrasound findings.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 736, doi. 10.1002/pd.377
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- Article
Prenatal prediction of childhood-onset spinal muscular atrophy (SMA) in Turkish families.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 703, doi. 10.1002/pd.384
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- Article
Prenatal detection of structural abnormalities of chromosome 18: associations with interphase fluorescence in situ hybridization (FISH) and maternal serum screening.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 645, doi. 10.1002/pd.354
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- Article
Prenatal diagnosis of a 45,X male with a SRY-bearing chromosome 21.
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- Prenatal Diagnosis, 2002, v. 22, n. 8, p. 675, doi. 10.1002/pd.376
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- Article