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Universal chromosomal microarray analysis reveals high proportion of copy-number variants in low-risk pregnancies.
- Published in:
- 2021
- By:
- Publication type:
- journal article
OC02.05: What is the chance for pathogenic chromosomal microarray analysis results in structurally normal fetuses?
- Published in:
- Ultrasound in Obstetrics & Gynecology, 2019, v. 54, p. 4, doi. 10.1002/uog.20433
- By:
- Publication type:
- Article
Clinicians' Attitudes toward General Screening of the Ashkenazi-Jewish Population for Prevalent Founder BRCA1/2 and LRRK2 Mutations.
- Published in:
- Public Health Genomics, 2013, v. 16, n. 4, p. 174, doi. 10.1159/000351592
- By:
- Publication type:
- Article
Common founder BRCA2 pathogenic variants and breast cancer characteristics in Ethiopian Jews.
- Published in:
- Breast Cancer Research & Treatment, 2022, v. 193, n. 1, p. 217, doi. 10.1007/s10549-022-06557-9
- By:
- Publication type:
- Article
Role of late amniocentesis in the era of modern genomic technologies.
- Published in:
- 2019
- By:
- Publication type:
- journal article
EP11.03: The impact of late amniocentesis in the chromosomal microarray era.
- Published in:
- Ultrasound in Obstetrics & Gynecology, 2018, v. 52, p. 243, doi. 10.1002/uog.19963
- By:
- Publication type:
- Article
OC20.07: Fetal exome sequencing: yield and limitations observed in a single tertiary centre.
- Published in:
- Ultrasound in Obstetrics & Gynecology, 2018, v. 52, p. 49, doi. 10.1002/uog.19345
- By:
- Publication type:
- Article
Abstracts of the 26th World Congress on Ultrasound in Obstetrics and Gynecology, Rome, Italy, 24-28 September 2016.
- Published in:
- 2016
- By:
- Publication type:
- journal article