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Prenatal diagnosis of diencephalic‐mesencephalic junction dysplasia: Fetal magnetic resonance imaging phenotypes, genetic diagnoses, and outcomes.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 778, doi. 10.1002/pd.5909
- By:
- Publication type:
- Article
Ultrasound diagnosis of oculo‐auriculo‐vertebral spectrum in a mid‐trimester foetus.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 791, doi. 10.1002/pd.5936
- By:
- Publication type:
- Article
Evaluation of the Z‐score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18 and 21 at a single center.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 690, doi. 10.1002/pd.5908
- By:
- Publication type:
- Article
Mosaicism for copy number variations in the placenta is even more difficult to interpret than mosaicism for whole chromosome aneuploidy.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 668, doi. 10.1002/pd.5938
- By:
- Publication type:
- Article
Performance of conventional cytogenetic analysis on chorionic villi when only one cell layer, cytotrophoblast or mesenchyme alone, is analyzed.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 652, doi. 10.1002/pd.5941
- By:
- Publication type:
- Article
Fetoscopic urethral meatotomy in fetuses with lower urinary tract obstruction by congenital megalourethra.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 772, doi. 10.1002/pd.5946
- By:
- Publication type:
- Article
Prenatal chromosome microarray: 'The UK experience'. A survey of reporting practices in UK genetic services (2012–2019).
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 661, doi. 10.1002/pd.5944
- By:
- Publication type:
- Article
Prenatal diagnosis and postnatal management of congenital mesoblastic nephroma: Experience at a single center in China.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 766, doi. 10.1002/pd.5942
- By:
- Publication type:
- Article
Health practitioners' perceptions of the barriers and enablers to the implementation of reproductive genetic carrier screening: A systematic review.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 708, doi. 10.1002/pd.5914
- By:
- Publication type:
- Article
Increasing prenatal diagnosis of chimeras with the use of noninvasive prenatal screening: Report of two cases.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 697, doi. 10.1002/pd.5911
- By:
- Publication type:
- Article
Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross‐sectional study with healthcare professionals.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 720, doi. 10.1002/pd.5932
- By:
- Publication type:
- Article
The diagnostic efficacy of exome data analysis using fixed neurodevelopmental gene lists: Implications for prenatal setting.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 701, doi. 10.1002/pd.5929
- By:
- Publication type:
- Article
The prognosis of common arterial trunk from a fetal perspective: A prenatal cohort study and systematic literature review.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 754, doi. 10.1002/pd.5907
- By:
- Publication type:
- Article
Health practitioners' perceptions of the barriers and enablers to the implementation of reproductive genetic carrier screening: A systematic review.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 708, doi. 10.1002/pd.5914
- By:
- Publication type:
- Article
Artificial intelligence, fetal echocardiography, and congenital heart disease.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 733, doi. 10.1002/pd.5892
- By:
- Publication type:
- Article
Feasibility study of using unbalanced embryos as a reference to distinguish euploid carrier from noncarrier embryos by single nucleotide polymorphism array for reciprocal translocations.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 681, doi. 10.1002/pd.5897
- By:
- Publication type:
- Article
Performance of conventional cytogenetic analysis on chorionic villi when only one cell layer, cytotrophoblast or mesenchyme alone, is analyzed.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Prenatal chromosome microarray: 'The UK experience'. A survey of reporting practices in UK genetic services (2012-2019).
- Published in:
- 2021
- By:
- Publication type:
- journal article
Noninvasive screening for congenital heart defects using a serum metabolomics approach.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 743, doi. 10.1002/pd.5893
- By:
- Publication type:
- Article
Mosaicism for copy number variations in the placenta is even more difficult to interpret than mosaicism for whole chromosome aneuploidy.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Obituary: Bruno Brambati, MD (29 February 1940‐3 August 2020).
- Published in:
- 2021
- By:
- Publication type:
- Obituary
Issue Information.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 649, doi. 10.1002/pd.5743
- Publication type:
- Article
Fetoscopic urethral meatotomy in fetuses with lower urinary tract obstruction by congenital megalourethra.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross-sectional study with healthcare professionals.
- Published in:
- 2021
- By:
- Publication type:
- journal article
The diagnostic efficacy of exome data analysis using fixed neurodevelopmental gene lists: Implications for prenatal setting.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Prenatal diagnosis and postnatal management of congenital mesoblastic nephroma: Experience at a single center in China.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Evaluation of the Z‐score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18 and 21 at a single center.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 690, doi. 10.1002/pd.5908
- By:
- Publication type:
- Article
Ultrasound diagnosis of oculo-auriculo-vertebral spectrum in a mid-trimester foetus.
- Published in:
- 2021
- By:
- Publication type:
- Letter
Increasing prenatal diagnosis of chimeras with the use of noninvasive prenatal screening: Report of two cases.
- Published in:
- 2021
- By:
- Publication type:
- journal article
The prognosis of common arterial trunk from a fetal perspective: A prenatal cohort study and systematic literature review.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Prenatal diagnosis of diencephalic-mesencephalic junction dysplasia: Fetal magnetic resonance imaging phenotypes, genetic diagnoses, and outcomes.
- Published in:
- 2021
- By:
- Publication type:
- journal article
Feasibility study of using unbalanced embryos as a reference to distinguish euploid carrier from noncarrier embryos by single nucleotide polymorphism array for reciprocal translocations.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 681, doi. 10.1002/pd.5897
- By:
- Publication type:
- Article
Noninvasive screening for congenital heart defects using a serum metabolomics approach.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 743, doi. 10.1002/pd.5893
- By:
- Publication type:
- Article
Artificial intelligence, fetal echocardiography, and congenital heart disease.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 733, doi. 10.1002/pd.5892
- By:
- Publication type:
- Article
Obituary: Bruno Brambati, MD (29 February 1940-3 August 2020).
- Published in:
- 2021
- By:
- Publication type:
- Editorial
Issue Information.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 6, p. 649, doi. 10.1002/pd.5743
- Publication type:
- Article