Found: 18
Select item for more details and to access through your institution.
Cover Image.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 1, doi. 10.1002/pd.6198
- By:
- Publication type:
- Article
Issue Information.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 805, doi. 10.1002/pd.5964
- Publication type:
- Article
The fetal sequencing consortium: The value of multidisciplinary dialog and collaboration.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 807, doi. 10.1002/pd.6190
- By:
- Publication type:
- Article
Parental mosaicism for apparent de novo genetic variants: Scope, detection, and counseling challenges.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 811, doi. 10.1002/pd.6144
- By:
- Publication type:
- Article
Diagnostic yield of genome sequencing for prenatal diagnosis of fetal structural anomalies.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 822, doi. 10.1002/pd.6108
- By:
- Publication type:
- Article
Lessons learnt from prenatal exome sequencing.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 831, doi. 10.1002/pd.6165
- By:
- Publication type:
- Article
Trio exome sequencing is highly relevant in prenatal diagnostics.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 845, doi. 10.1002/pd.6081
- By:
- Publication type:
- Article
Diagnostic yield of whole exome data in fetuses aborted for conotruncal malformations.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 852, doi. 10.1002/pd.6147
- By:
- Publication type:
- Article
Exploring the diagnostic utility of genome sequencing for fetal congenital heart defects.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 862, doi. 10.1002/pd.6151
- By:
- Publication type:
- Article
Prenatal diagnosis for fetuses with isolated and non‐isolated congenital heart defects using chromosomal microarray and exome sequencing.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 873, doi. 10.1002/pd.6168
- By:
- Publication type:
- Article
The many etiologies of nonimmune hydrops fetalis diagnosed by exome sequencing.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 881, doi. 10.1002/pd.5977
- By:
- Publication type:
- Article
Non‐immune hydrops fetalis caused by PIEZO1 compound heterozygous deletions detected only by exome sequencing.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 890, doi. 10.1002/pd.6142
- By:
- Publication type:
- Article
Genetic diagnosis of common fetal renal abnormalities detected on prenatal ultrasound.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 894, doi. 10.1002/pd.6154
- By:
- Publication type:
- Article
A single center experience of prenatal parent‐fetus trio exome sequencing for pregnancies with congenital anomalies.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 901, doi. 10.1002/pd.6170
- By:
- Publication type:
- Article
Fetal phenotypes of Mendelian disorders: A descriptive study from India.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 911, doi. 10.1002/pd.6172
- By:
- Publication type:
- Article
Family history is key to the interpretation of exome sequencing in the prenatal context: unexpected diagnosis of Basal Cell Nevus Syndrome.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 927, doi. 10.1002/pd.6171
- By:
- Publication type:
- Article
Factors that impact on women's decision‐making around prenatal genomic tests: An international discrete choice survey.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 934, doi. 10.1002/pd.6159
- By:
- Publication type:
- Article
Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomalies.
- Published in:
- Prenatal Diagnosis, 2022, v. 42, n. 7, p. 947, doi. 10.1002/pd.6153
- By:
- Publication type:
- Article