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HARVARD Citation
Lee, H. et al. (2020). Identification of rare missense mutations in NOTCH2 and HERC2 associated with familial central precocious puberty via whole-exome sequencing. Gynecological endocrinology. pp. 682-686. [Online].
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Lee, H. et al. (2020). Identification of rare missense mutations in NOTCH2 and HERC2 associated with familial central precocious puberty via whole-exome sequencing. Gynecological endocrinology. pp. 682-686. [Online].