Cite
HARVARD Citation
Bruel, A. et al. (2017). Autosomal recessive truncating MAB21L1 mutation associated with a syndromic scrotal agenesis. Clinical genetics. 91 (2), pp. 333-338. [Online].
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Bruel, A. et al. (2017). Autosomal recessive truncating MAB21L1 mutation associated with a syndromic scrotal agenesis. Clinical genetics. 91 (2), pp. 333-338. [Online].