Found: 13
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Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Increased nuchal translucency origins from abnormal lymphatic development and is independent of the presence of a cardiac defect.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Improving spectral quality in fetal brain magnetic resonance spectroscopy using constructive averaging.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Double-factor preimplantation genetic diagnosis: monogenic and cytogenetic diagnoses analyzing a single blastomere.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Screening performances of abnormal first-trimester ductus venosus blood flow and increased nuchal translucency thickness in detection of major heart defects.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Amniotic fluid biochemistry in isolated polyhydramnios: a series of 464 cases.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Should we offer prenatal testing for 17q12 microdeletion syndrome to all cases with prenatally diagnosed echogenic kidneys? Prenatal findings in two families with 17q12 microdeletion syndrome and review of the literature.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Challenges in prenatal diagnosis of beta thalassaemia: couples with normal HbA2 in one partner.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Perinatal outcomes of fetal pleural effusion following thoracoamniotic shunting.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Prenatal serum screening markers may not require adjustment in former smokers.
- Published in:
- 2015
- By:
- Publication type:
- letter
Good prenatal detection rate of major birth defects in HIV-infected pregnant women in Italy.
- Published in:
- 2015
- By:
- Publication type:
- letter
A homozygous PAX3 mutation leading to severe presentation of Waardenburg syndrome with a prenatal diagnosis.
- Published in:
- 2015
- By:
- Publication type:
- case study
List of reviewers for Prenatal Diagnosis, January 2015-December 2015.
- Published in:
- 2015
- Publication type:
- journal article