Found: 21
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Invasive testing for the karyotyping of mid-trimester intrauterine fetal death (IUFD): a pilot study.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 453, doi. 10.1002/pd.339
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- Article
Improving the prenatal diagnosis of citrullinemia using citrulline/ornithine+arginine ratio in amniotic fluid.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 456, doi. 10.1002/pd.344
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- Article
Pilot study for the neonatal screening of fragile X syndrome.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 459, doi. 10.1002/pd.346
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- Article
Expandability of haemopoietic progenitors in first trimester fetal and maternal blood: implications for non-invasive prenatal diagnosis.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 463, doi. 10.1002/pd.350
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- Article
Pallister-Killian syndrome: difficulties of prenatal diagnosis.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 470, doi. 10.1002/pd.342
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- Article
The role of hyperglycosylated hCG in trophoblast invasion and the prediction of subsequent pre-eclampsia.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 478, doi. 10.1002/pd.329
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- Article
An increase in cost-effectiveness of first trimester maternal screening programmes for fetal chromosome anomalies is obtained by contingent testing.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 482, doi. 10.1002/pd.336
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- Article
First prenatal diagnosis of partial trisomy 10 and partial monosomy 15 derived from a maternal translocation (10;15)(q11;q13).
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 487, doi. 10.1002/pd.343
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- Article
In utero first trimester exposure to low-dose methotrexate with increased fetal nuchal translucency and associated malformations.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 489, doi. 10.1002/pd.334
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- Article
Brain anomalies associated with 47,XYY karyotypes detected on a prenatal scan.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 490, doi. 10.1002/pd.332
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- Article
Trisomy 18 in a fetus with normal NT and abnormal maternal serum biochemistry.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 492, doi. 10.1002/pd.338
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- Article
Mucopolysaccharidosis VII (Sly disease) as a cause of increased nuchal translucency and non-immune fetal hydrops: study of a family and technical approach to prenatal diagnosis in early and late pregnancy.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 493, doi. 10.1002/pd.330
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- Article
Varix of the portal vein: prenatal diagnosis in a fetus with mosaic trisomy 9 syndrome.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 495, doi. 10.1002/pd.317
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- Article
Two more possible pitfalls of rapid prenatal diagnostics using interphase nuclei.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 497, doi. 10.1002/pd.299
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- Article
Application of monopolar thermocoagulation in an acardiac fetus.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 499, doi. 10.1002/pd.349
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- Article
Non-disclosing preimplantation genetic diagnosis for Huntington disease.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 503, doi. 10.1002/pd.359
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- Article
Attitude of at-risk subjects towards preimplantation genetic diagnosis of α- and β-thalassaemias in Hong Kong.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 508, doi. 10.1002/pd.387
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- Article
Preimplantation genetic diagnosis for aneuploidy screening in early human embryos: a review.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 512, doi. 10.1002/pd.388
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- Article
First application of preimplantation genetic diagnosis to neurofibromatosis type 2 (NF2).
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 519, doi. 10.1002/pd.393
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- Article
Preimplantation genetic diagnosis for single gene disorders: experience with five single gene disorders.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 525, doi. 10.1002/pd.394
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- Article
Current Awareness.
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- Prenatal Diagnosis, 2002, v. 22, n. 6, p. 534, doi. 10.1002/pd.269
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- Article