Cite
HARVARD Citation
Christensen, M. et al. (2022). Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder. Clinical genetics. 102 (2), pp. 98-109. [Online].
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Christensen, M. et al. (2022). Biallelic variants in ZNF142 lead to a syndromic neurodevelopmental disorder. Clinical genetics. 102 (2), pp. 98-109. [Online].