Found: 16
Select item for more details and to access through your institution.
Survival rates and outcomes of pregnancies with prenatal diagnosis of trisomy 18: A 16‐year experience from a public hospital in South Africa.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 13, p. 1643, doi. 10.1002/pd.6270
- By:
- Publication type:
- Article
Positive predictive values and outcomes for uninformative cell‐free DNA tests: An Italian multicentric Cytogenetic and cytogenomic Audit of diagnOstic testing (ICARO study).
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 13, p. 1575, doi. 10.1002/pd.6271
- By:
- Publication type:
- Article
Prenatal phenotype of FBXL4‐associated encephalomyopathic mitochondrial DNA depletion syndrome‐13.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 13, p. 1682, doi. 10.1002/pd.6272
- By:
- Publication type:
- Article
Prenatal phenotyping of fetal tubulinopathies: A multicenter retrospective case series.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 13, p. 1686, doi. 10.1002/pd.6269
- By:
- Publication type:
- Article
Copy number variations analysis in a cohort of 47 fetuses and newborns with congenital diaphragmatic hernia.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 13, p. 1627, doi. 10.1002/pd.6268
- By:
- Publication type:
- Article
Do reproductive history and information given through genetic counselling influence patients' decisions on mosaic embryo transfer?
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 13, p. 1650, doi. 10.1002/pd.6267
- By:
- Publication type:
- Article
Fetal cerebral ventriculomegaly: What do we tell the prospective parents?
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 13, p. 1674, doi. 10.1002/pd.6266
- By:
- Publication type:
- Article
Positive predictive value of a single nucleotide polymorphism (SNP)‐based NIPT for aneuploidy in twins: Experience from clinical practice.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 13, p. 1587, doi. 10.1002/pd.6262
- By:
- Publication type:
- Article
Tricky TRIC: A replication study using trophoblast retrieval and isolation from the cervix to study genetic birth defects.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 13, p. 1612, doi. 10.1002/pd.6260
- By:
- Publication type:
- Article
Prenatal isolated clubfoot increases the risk for clinically significant exome sequencing results.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 13, p. 1622, doi. 10.1002/pd.6259
- By:
- Publication type:
- Article
Prenatal intracranial hypotension syndrome in congenital cephalocele: Insights into pathophysiologic mechanisms and importance of defect coverage.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 13, p. 1667, doi. 10.1002/pd.6258
- By:
- Publication type:
- Article
The impact of maternal and geographical factors on the uptake of non‐invasive prenatal testing: A retrospective cohort study.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 13, p. 1594, doi. 10.1002/pd.6257
- By:
- Publication type:
- Article
Increased use of diagnostic testing after increased nuchal translucency: The influence of non‐invasive prenatal testing and chromosomal microarray.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 13, p. 1606, doi. 10.1002/pd.6255
- By:
- Publication type:
- Article
Prenatal diagnosis of fetal ectopia cordis by fetal cardiovascular magnetic resonance imaging.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Views of reproductive genetic carrier screening participants regarding screening for genes associated with non‐syndromic hearing loss.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 13, p. 1658, doi. 10.1002/pd.6253
- By:
- Publication type:
- Article
Issue Information.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 13, p. 1573, doi. 10.1002/pd.5970
- Publication type:
- Article