Exome sequencing in 90 children with developmental delay: a single-center experience
Our findings emphasize the utility of WES in clinical diagnostics, offering significant insights into patient management and potentially guiding therapeutic decisions.
Authors
- Oksana Boyarchuk (ORCID: https://orcid.org/0000-0002-1234-0040)
- Olena Smashna (ORCID: https://orcid.org/0000-0001-6595-2940)
- L.A. Volianska (ORCID: https://orcid.org/0000-0001-5447-8059)
- Halyna Makukh (ORCID: https://orcid.org/0000-0001-7749-5353)
Institutions
- I.Horbachevsky Ternopil National Medical University (UA)
Publication Details
- Journal
- Frontiers in Genetics
- Published
- 2024-11-29
- DOI
- https://doi.org/10.3389/fgene.2024.1505254
- Citations
- 2
- Primary Topic
- Genomics and Rare Diseases
- Type
- article
- Field-Weighted Citation Impact
- 1.10