Cite
HARVARD Citation
He, W. et al. (2018). DMC1 mutation that causes human non-obstructive azoospermia and premature ovarian insufficiency identified by whole-exome sequencing. Journal of medical genetics. 55 (3), pp. 198-204. [Online].
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He, W. et al. (2018). DMC1 mutation that causes human non-obstructive azoospermia and premature ovarian insufficiency identified by whole-exome sequencing. Journal of medical genetics. 55 (3), pp. 198-204. [Online].