Investigation of the molecular genetic causes of non-syndromic primary ovarian ınsufficiency by next generation sequencing analysis.
- DOI
- 10.20945/2359-4292-2022-0475
- Published
- 2023 Nov 17
- Container
- Archives of endocrinology and metabolism
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.20945/2359-4292-2022-0475,
title = {Investigation of the molecular genetic causes of non-syndromic primary ovarian ınsufficiency by next generation sequencing analysis.},
author = {Er E and Aşıkovalı S and Özışık H and Sağsak E and GÖkşen D and Onay H and Saygılı F and Darcan Ş and Özen S},
year = {2023},
journal = {Archives of endocrinology and metabolism},
doi = {10.20945/2359-4292-2022-0475},
url = {https://doi.org/10.20945/2359-4292-2022-0475}
}RIS
TY - JOUR TI - Investigation of the molecular genetic causes of non-syndromic primary ovarian ınsufficiency by next generation sequencing analysis. AU - Er E AU - Aşıkovalı S AU - Özışık H AU - Sağsak E AU - GÖkşen D AU - Onay H AU - Saygılı F AU - Darcan Ş AU - Özen S PY - 2023 JO - Archives of endocrinology and metabolism DO - 10.20945/2359-4292-2022-0475 UR - https://doi.org/10.20945/2359-4292-2022-0475 ER -
APA
E, E., S, A., H, Ö., E, S., D, G., H, O., F, S., Ş, D., & S, Ö. (2023). Investigation of the molecular genetic causes of non-syndromic primary ovarian ınsufficiency by next generation sequencing analysis.. Archives of endocrinology and metabolism. https://doi.org/10.20945/2359-4292-2022-0475
Source records
- pubmed · retrieved 2026-09-26T01:47:34.491Z