Non‐invasive prenatal test uptake in socioeconomically disadvantaged neighborhoods.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 11, p. 1395, doi. 10.1002/pd.6043
- By:
- Publication type:
- Article
Works matching IS 01973851 AND DT 2021 AND VI 41 AND IP 11
Results: 15
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Predicting neonatal outcomes in infants with giant omphalocele using prenatal magnetic resonance imaging calculated observed‐to‐expected fetal lung volumes.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 11, p. 1439, doi. 10.1002/pd.6040
- By:
- Publication type:
- Article
3
Severe early‐onset fetal growth restriction: What do we tell the prospective parents?
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 11, p. 1363, doi. 10.1002/pd.6030
- By:
- Publication type:
- Article
4
Incidence of childhood hearing loss after in utero exposure to platinum agents.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 11, p. 1467, doi. 10.1002/pd.6035
- By:
- Publication type:
- Article
5
Counseling for personal health implications identified during reproductive genetic carrier screening.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 11, p. 1460, doi. 10.1002/pd.6033
- By:
- Publication type:
- Article
6
Racial and ethnic differences in uptake of cell‐free fetal DNA aneuploidy screening in an urban safety net hospital.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 11, p. 1389, doi. 10.1002/pd.6029
- By:
- Publication type:
- Article
7
The cost‐effectiveness of genotyping versus sequencing for prenatal cystic fibrosis carrier screening.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 11, p. 1449, doi. 10.1002/pd.6027
- By:
- Publication type:
- Article
8
Factors associated with poor outcome in fetuses prenatally diagnosed with sacrococcygeal teratoma.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 11, p. 1430, doi. 10.1002/pd.6026
- By:
- Publication type:
- Article
9
Utility of fetal whole exome sequencing in the etiological evaluation and outcome of nonimmune hydrops fetalis.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 11, p. 1414, doi. 10.1002/pd.6022
- By:
- Publication type:
- Article
10
Exome‐based preconception carrier testing for consanguineous couples in China.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 11, p. 1425, doi. 10.1002/pd.6018
- By:
- Publication type:
- Article
11
Neonatal caudal regression syndrome.
- Published in:
- 2021
- By:
- Publication type:
- journal article
12
Not all low fetal fraction cell‐free DNA screening failures are at increased risk for aneuploidy.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 11, p. 1372, doi. 10.1002/pd.5918
- By:
- Publication type:
- Article
13
Prenatal prediction of fetal Rh C, c and E status by amplification of maternal cfDNA and deep sequencing.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 11, p. 1380, doi. 10.1002/pd.5976
- By:
- Publication type:
- Article
14
Combined exome sequencing and deep phenotyping in highly selected fetuses with skeletal dysplasia during the first and second trimesters improves diagnostic yield.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 11, p. 1401, doi. 10.1002/pd.5974
- By:
- Publication type:
- Article
15
Issue Information.
- Published in:
- Prenatal Diagnosis, 2021, v. 41, n. 11, p. 1361, doi. 10.1002/pd.5748
- Publication type:
- Article