Found: 22
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Wolf-Hirschhorn syndrome due to a 3:1 segregation of a maternal balanced t(4;15)(p16.3;q11) translocation.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 847, doi. 10.1002/1097-0223(200010)20:10<847::AID-PD930>3.0.CO;2-O
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- Article
First trimester markers of trisomy 21 and the influence of maternal cigarette smoking status.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 852, doi. 10.1002/1097-0223(200010)20:10<852::AID-PD941>3.0.CO;2-M
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Evaluation of the prenatal diagnosis of limb reduction deficiencies.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 811, doi. 10.1002/1097-0223(200010)20:10<811::AID-PD927>3.0.CO;2-J
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Fetal DNA in maternal plasma is elevated in pregnancies with aneuploid fetuses.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 795, doi. 10.1002/1097-0223(200010)20:10<795::AID-PD897>3.0.CO;2-P
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High levels of fetal erythroblasts and fetal extracellular DNA in the peripheral blood of a pregnant woman with idiopathic polyhydramnios: case report.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 838, doi. 10.1002/1097-0223(200010)20:10<838::AID-PD911>3.0.CO;2-P
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Response to Hallahan et al.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 790, doi. 10.1002/1097-0223(200010)20:10<790::AID-PD922>3.0.CO;2-C
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Current Awareness.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 857, doi. 10.1002/1097-0223(200010)20:10<857::AID-PD834>3.0.CO;2-C
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- Article
Incidental prenatal detection of an Xp deletion using an anonymous primer pair for fetal sexing.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 842, doi. 10.1002/1097-0223(200010)20:10<842::AID-PD915>3.0.CO;2-G
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Normal outcome after prenatal diagnosis of thrombosis of the torcular Herophili.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 824, doi. 10.1002/1097-0223(200010)20:10<824::AID-PD926>3.0.CO;2-G
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- Article
First trimester biochemical screening for Down syndrome: free beta hCG versus intact hCG.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 785, doi. 10.1002/1097-0223(200010)20:10<785::AID-PD892>3.0.CO;2-6
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- Article
False-positive maternal serum screening in systemic lupus erythematosis: a case report.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 851, doi. 10.1002/1097-0223(200010)20:10<851::AID-PD932>3.0.CO;2-L
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- Article
Prenatal diagnosis of the neuronal ceroid lipofuscinoses.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 819, doi. 10.1002/1097-0223(200010)20:10<819::AID-PD933>3.0.CO;2-M
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- Article
Fetus with a 9q22q34 interstitial deletion and hygroma.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 855, doi. 10.1002/1097-0223(200010)20:10<855::AID-PD919>3.0.CO;2-Z
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- Article
Genetic analysis of fetal nucleated red blood cells from CVS washings.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 832, doi. 10.1002/1097-0223(200010)20:10<832::AID-PD921>3.0.CO;2-U
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Combined first trimester nuchal translucency and second trimester biochemical screening tests among normal pregnancies.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 781, doi. 10.1002/1097-0223(200010)20:10<781::AID-PD908>3.0.CO;2-Z
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Sonographic and molecular diagnosis of thanatophoric dysplasia type I at 18 weeks of gestation.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 835, doi. 10.1002/1097-0223(200010)20:10<835::AID-PD903>3.0.CO;2-N
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The influence of parity and gravidity on first trimester markers of chromosomal abnormality.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 792, doi. 10.1002/1097-0223(200010)20:10<792::AID-PD914>3.0.CO;2-5
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Management of fetal thyroid goitres: a report of 11 cases in a single perinatal unit.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 799, doi. 10.1002/1097-0223(200010)20:10<799::AID-PD925>3.0.CO;2-V
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Early prenatal diagnosis of the ICF syndrome.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 828, doi. 10.1002/1097-0223(200010)20:10<828::AID-PD907>3.0.CO;2-B
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A novel mutation detected by temporal temperature gradient gel electrophoresis led to the confirmative prenatal diagnosis of a Hispanic CF family.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 807, doi. 10.1002/1097-0223(200010)20:10<807::AID-PD929>3.0.CO;2-A
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Prenatal diagnosis of X-linked hyper-IGM syndrome by direct detection of mutation Q220X in the CD40L gene using PCR-mediated site directed mutagenesis.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 822, doi. 10.1002/1097-0223(200010)20:10<822::AID-PD935>3.0.CO;2-K
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Prenatal diagnosis of fragile X and Turner mosaicism in a 12-week fetus.
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- Prenatal Diagnosis, 2000, v. 20, n. 10, p. 854, doi. 10.1002/1097-0223(200010)20:10<854::AID-PD928>3.0.CO;2-1
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