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HARVARD Citation
Karakaya, C. et al. (2022). Further delineation of familial polycystic ovary syndrome (PCOS) via whole‐exome sequencing: PCOS‐related rare FBN3 and FN1 gene variants are identified. Journal of obstetrics and gynaecology research. 48 (5), pp. 1202-1211. [Online].