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HARVARD Citation
Simon, D. et al. (2016). Mutations in the maternally imprinted gene MKRN3 are common in familial central precocious puberty. European journal of endocrinology. 174 (1), pp. 1-8. [Online].
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Simon, D. et al. (2016). Mutations in the maternally imprinted gene MKRN3 are common in familial central precocious puberty. European journal of endocrinology. 174 (1), pp. 1-8. [Online].