DOI: 10.1055/s-00000072

Seminars in Reproductive Medicine

References

Tan YQ, Tu C, Meng L. et al.
Loss-of-function mutations in TDRD7 lead to a rare novel syndrome combining congenital cataract and nonobstructive azoospermia in humans.

Genet Med 2019;
21 (05) 1209-1217

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