Found: 3
Select item for more details and to access through your institution.
Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil.
- Published in:
- Scientific Reports, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41598-022-19274-6
- By:
- Publication type:
- Article
Low‐pass whole genome sequencing is a reliable and cost‐effective approach for copy number variant analysis in the clinical setting.
- Published in:
- Annals of Human Genetics, 2024, v. 88, n. 2, p. 113, doi. 10.1111/ahg.12532
- By:
- Publication type:
- Article
Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses.
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 8, p. 2335, doi. 10.1002/ajmg.a.62237
- By:
- Publication type:
- Article