Found: 21
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Non-invasive fetal RHD and RHCE genotyping from maternal plasma in alloimmunized pregnancies.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 12, p. 1079, doi. 10.1002/pd.1282
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- Publication type:
- Article
Prenatal detection of deletion 6q13q15 in a complex karyotype.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 12, p. 1084, doi. 10.1002/pd.1265
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- Publication type:
- Article
Vascular-type disruptive defects in fetuses with homozygous alpha-thalassemia: report of two cases and review of the literature.
- Published in:
- 2005
- By:
- Publication type:
- journal article
MRI supported diagnosis and counselling in a family with a probably autosomal recessive form of pachygyria.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 12, p. 1097, doi. 10.1002/pd.1244
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- Publication type:
- Article
Predicting the result of additional second-trimester markers from a woman's first-trimester marker profile: a new concept in Down syndrome screening.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 12, p. 1102, doi. 10.1002/pd.1256
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- Publication type:
- Article
Successful outcome following prenatal intervention in a female fetus with bladder outlet obstruction.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 12, p. 1107, doi. 10.1002/pd.1285
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- Publication type:
- Article
Reduction in diagnostic and therapeutic interventions by non-invasive determination of fetal sex in early pregnancy.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 12, p. 1111, doi. 10.1002/pd.1284
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- Publication type:
- Article
First prenatal molecular diagnosis in a family with holocarboxylase synthetase deficiency.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 12, p. 1117, doi. 10.1002/pd.1291
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- Publication type:
- Article
Recurrences of free trisomy 21: analysis of data from the National Down Syndrome Cytogenetic Register.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 12, p. 1120, doi. 10.1002/pd.1292
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- Publication type:
- Article
First-trimester fetal heart block and increased nuchal translucency: an indication for early fetal echocardiography.
- Published in:
- 2005
- By:
- Publication type:
- journal article
Prenatal diagnosis of monosomy 4p14→pter and trisomy 11q25→qter: clinical presentations and outcomes.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 12, p. 1133, doi. 10.1002/pd.1287
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- Publication type:
- Article
Rapid determination of trisomy 21 from amniotic fluid cells using single-nucleotide polymorphic loci.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 12, p. 1138, doi. 10.1002/pd.1288
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- Publication type:
- Article
Complex de novo cryptic subtelomeric rearrangements in a fetus with multiple ultrasonographic abnormalities and a normal karyotype at amniocentesis.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 12, p. 1142, doi. 10.1002/pd.1290
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- Publication type:
- Article
Prenatal forehead edema in 4p- deletion: the 'Greek warrior helmet' profile revisited.
- Published in:
- 2005
- By:
- Publication type:
- journal article
First-trimester screening for trisomy 21 in twin pregnancy: does the addition of biochemistry make an improvement?
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 12, p. 1156, doi. 10.1002/pd.1304
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- Publication type:
- Article
Integrated serum screening for Down syndrome in primary obstetric practice.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 12, p. 1162, doi. 10.1002/pd.1305
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- Publication type:
- Article
Which contingent sequential screening protocol?
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 12, p. 1168, doi. 10.1002/pd.1275
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- Publication type:
- Article
Which contingent sequential screening protocol?: A response.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 12, p. 1169, doi. 10.1002/pd.1370
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- Publication type:
- Article
Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 → pter) and partial monosomy 9p (9p22 → pter).
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 12, p. 1170, doi. 10.1002/pd.1300
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- Publication type:
- Article
Concomitant fetal anemia and thrombocytopenia due to anti-D and anti-HPA1a alloimmunization.
- Published in:
- 2005
- By:
- Publication type:
- case study
Current awareness in prenatal diagnosis.
- Published in:
- Prenatal Diagnosis, 2005, v. 25, n. 12, p. 1175, doi. 10.1002/pd.1026
- Publication type:
- Article