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HARVARD Citation
Caburet, S. et al. (2017). A homozygous mutation of GNRHR in a familial case diagnosed with polycystic ovary syndrome. European journal of endocrinology. 176 (5), pp. K9-K14. [Online].
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Caburet, S. et al. (2017). A homozygous mutation of GNRHR in a familial case diagnosed with polycystic ovary syndrome. European journal of endocrinology. 176 (5), pp. K9-K14. [Online].