Found: 19
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(Potential) false-negative diagnoses in chorionic villi and a review of the literature.
- Published in:
- Prenatal Diagnosis, 2006, v. 26, n. 5, p. 401, doi. 10.1002/pd.1421
- By:
- Publication type:
- Article
The consanguinity effect on QF-PCR diagnosis of autosomal anomalies.
- Published in:
- Prenatal Diagnosis, 2006, v. 26, n. 5, p. 409, doi. 10.1002/pd.1424
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- Publication type:
- Article
Prenatal diagnosis of Fukuyama congenital muscular dystrophy.
- Published in:
- 2006
- By:
- Publication type:
- Other
Prenatal diagnosis of a mosaic supernumerary marker iso (8p) (tetrasomy 8p): discordance between chorionic villi culture and amniotic fluid karyotypes.
- Published in:
- Prenatal Diagnosis, 2006, v. 26, n. 5, p. 418, doi. 10.1002/pd.1427
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- Publication type:
- Article
Association of Clinical Cytogeneticists chorion villus sampling database 1987-2000.
- Published in:
- Prenatal Diagnosis, 2006, v. 26, n. 5, p. 420, doi. 10.1002/pd.1429
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- Publication type:
- Article
Confined placental mosaicism as a risk factor among newborns with fetal growth restriction.
- Published in:
- Prenatal Diagnosis, 2006, v. 26, n. 5, p. 428, doi. 10.1002/pd.1430
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- Publication type:
- Article
Determinants of flow along arterio-arterial anastomoses in monochorionic placentae by dynamic computer modelling of chorionic plate vasculature.
- Published in:
- 2006
- By:
- Publication type:
- journal article
Health and developmental outcome of children following prenatal diagnosis of confined placental mosaicism.
- Published in:
- Prenatal Diagnosis, 2006, v. 26, n. 5, p. 443, doi. 10.1002/pd.1433
- By:
- Publication type:
- Article
Prenatal diagnosis of primary microcephaly in two consanguineous families by confrontation of morphometry with DNA data.
- Published in:
- 2006
- By:
- Publication type:
- journal article
Variable outcomes in mosaic trisomy 16: five case reports and literature analysis.
- Published in:
- Prenatal Diagnosis, 2006, v. 26, n. 5, p. 454, doi. 10.1002/pd.1437
- By:
- Publication type:
- Article
X-linked fetal cardiomyopathy caused by a novel mutation in the TAZ gene.
- Published in:
- 2006
- By:
- Publication type:
- journal article
Rapid genetic analysis of oculocutaneous albinism (OCA1) using denaturing high performance liquid chromatography (DHPLC) system.
- Published in:
- Prenatal Diagnosis, 2006, v. 26, n. 5, p. 466, doi. 10.1002/pd.1439
- By:
- Publication type:
- Article
Fetal serum β2-microglobulin as a marker for fetal infectious diseases.
- Published in:
- Prenatal Diagnosis, 2006, v. 26, n. 5, p. 471, doi. 10.1002/pd.1441
- By:
- Publication type:
- Article
Fetal echocardiography during routine first-trimester screening: a feasibility study in an unselected population.
- Published in:
- 2006
- By:
- Publication type:
- journal article
Congenital heart defects associated with fetal trisomy 18.
- Published in:
- 2006
- By:
- Publication type:
- letter
Prenatal diagnosis of congenital immature teratoma arising from retroperitoneum.
- Published in:
- 2006
- By:
- Publication type:
- case study
Immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome (IPEX): report of the first prenatal mutation testing.
- Published in:
- 2006
- By:
- Publication type:
- case study
Prenatal sonography and magnetic resonance imaging of pulmonary sequestration associated with a gastric duplication cyst.
- Published in:
- 2006
- By:
- Publication type:
- case study
Current awareness in prenatal diagnosis.
- Published in:
- 2006
- Publication type:
- bibliography