Cite
HARVARD Citation
He, W. et al. (2018). Whole‐exome sequencing identifies a homozygous donor splice‐site mutation in STAG3 that causes primary ovarian insufficiency. Clinical genetics. 93 (2), pp. 340-344. [Online].
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He, W. et al. (2018). Whole‐exome sequencing identifies a homozygous donor splice‐site mutation in STAG3 that causes primary ovarian insufficiency. Clinical genetics. 93 (2), pp. 340-344. [Online].