Found: 17
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Screening for trisomy 21 in twin pregnancies in the first trimester using free β-hCG and PAPP-A, combined with fetal nuchal translucency thickness.
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- Prenatal Diagnosis, 2000, v. 20, n. 2, p. 91, doi. 10.1002/(SICI)1097-0223(200002)20:2<91::AID-PD759>3.0.CO;2-X
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- Article
Serum screening for Down syndrome and adverse pregnancy outcomes: a case-controlled study.
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- Prenatal Diagnosis, 2000, v. 20, n. 2, p. 96, doi. 10.1002/(SICI)1097-0223(200002)20:2<96::AID-PD766>3.0.CO;2-#
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Maternal serum second trimester AFP and hCG in pregnancies with placenta previa.
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- Prenatal Diagnosis, 2000, v. 20, n. 2, p. 100, doi. 10.1002/(SICI)1097-0223(200002)20:2<100::AID-PD767>3.0.CO;2-5
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Common trisomy mosaicism diagnosed in amniocytes involving chromosomes 13, 18, 20 and 21: karyotype-phenotype correlations.
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- Prenatal Diagnosis, 2000, v. 20, n. 2, p. 103, doi. 10.1002/(SICI)1097-0223(200002)20:2<103::AID-PD761>3.0.CO;2-K
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Analysis of uncultured amniocytes by comparative genomic hybridization: a prospective prenatal study.
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- Prenatal Diagnosis, 2000, v. 20, n. 2, p. 123, doi. 10.1002/(SICI)1097-0223(200002)20:2<123::AID-PD762>3.0.CO;2-B
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- Article
Haplotype association and mutation analysis of the transglutaminase 1 gene for prenatal exclusion of lamellar ichthyosis.
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- Prenatal Diagnosis, 2000, v. 20, n. 2, p. 132, doi. 10.1002/(SICI)1097-0223(200002)20:2<132::AID-PD765>3.0.CO;2-0
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Characterization and clinical implications of marker chromosomes identified at prenatal diagnosis.
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- Prenatal Diagnosis, 2000, v. 20, n. 2, p. 138, doi. 10.1002/(SICI)1097-0223(200002)20:2<138::AID-PD772>3.0.CO;2-2
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Inherited interstitial deletion of chromosomes 5p and 16q without apparent phenotypic effect: further confirmation.
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- Prenatal Diagnosis, 2000, v. 20, n. 2, p. 144, doi. 10.1002/(SICI)1097-0223(200002)20:2<144::AID-PD770>3.0.CO;2-9
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Prenatal diagnosis and management of orofacial clefts.
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- Prenatal Diagnosis, 2000, v. 20, n. 2, p. 149, doi. 10.1002/(SICI)1097-0223(200002)20:2<149::AID-PD764>3.0.CO;2-U
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Prenatal diagnosis of a fetus with a cryptic translocation 4p;18p and Wolf-Hirschhorn syndrome (WHS).
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- Prenatal Diagnosis, 2000, v. 20, n. 2, p. 152, doi. 10.1002/(SICI)1097-0223(200002)20:2<152::AID-PD738>3.0.CO;2-P
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Dicentric marker derived from chromosome 22 associated with mild clinical signs: a case report.
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- Prenatal Diagnosis, 2000, v. 20, n. 2, p. 156, doi. 10.1002/(SICI)1097-0223(200002)20:2<156::AID-PD758>3.0.CO;2-J
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Relative efficiency of FISH on metaphase and interphase nuclei from non-mosaic trisomic or triploid fibroblast cultures.
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- Prenatal Diagnosis, 2000, v. 20, n. 2, p. 159, doi. 10.1002/(SICI)1097-0223(200002)20:2<159::AID-PD760>3.0.CO;2-2
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- Article
Prenatal diagnosis of abdominal enteric duplications.
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- Prenatal Diagnosis, 2000, v. 20, n. 2, p. 163, doi. 10.1002/(SICI)1097-0223(200002)20:2<163::AID-PD769>3.0.CO;2-F
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Plasma measurement of 7-dehydrocholesterol to detect carriers of Smith-Lemli-Opitz syndrome.
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- Prenatal Diagnosis, 2000, v. 20, n. 2, p. 168, doi. 10.1002/(SICI)1097-0223(200002)20:2<168::AID-PD749>3.0.CO;2-C
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Maternal age-specific rates of Down syndrome used in serum screening are biased low.
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- Prenatal Diagnosis, 2000, v. 20, n. 2, p. 169, doi. 10.1002/(SICI)1097-0223(200002)20:2<169::AID-PD771>3.0.CO;2-W
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A false positive diagnosis of conjoined twins in a triplet pregnancy: pitfalls of first trimester ultrasonographic prenatal diagnosis.
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- Prenatal Diagnosis, 2000, v. 20, n. 2, p. 169, doi. 10.1002/(SICI)1097-0223(200002)20:2<169::AID-PD768>3.0.CO;2-C
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Current Awareness.
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- Prenatal Diagnosis, 2000, v. 20, n. 2, p. 171, doi. 10.1002/(SICI)1097-0223(200002)20:2<171::AID-PD826>3.0.CO;2-O
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- Article