van der Laan, L. Et Al. 2025. CUL3-related neurodevelopmental disorder: Clinical phenotype of 20 new individuals and identification of a potential phenotype-associated episignature. HUMAN GENETICS AND GENOMICS ADVANCES , vol.6, no.1 .

van der Laan, L., Silva, A., Kleinendorst, L., Rooney, K., Haghshenas, S., Lauffer, P., ... Alanay, Y.(2025). CUL3-related neurodevelopmental disorder: Clinical phenotype of 20 new individuals and identification of a potential phenotype-associated episignature. HUMAN GENETICS AND GENOMICS ADVANCES , vol.6, no.1.

van der Laan, Liselot Et Al. "CUL3-related neurodevelopmental disorder: Clinical phenotype of 20 new individuals and identification of a potential phenotype-associated episignature," HUMAN GENETICS AND GENOMICS ADVANCES , vol.6, no.1, 2025

van der Laan, Liselot v. Et Al. "CUL3-related neurodevelopmental disorder: Clinical phenotype of 20 new individuals and identification of a potential phenotype-associated episignature." HUMAN GENETICS AND GENOMICS ADVANCES , vol.6, no.1, 2025

van der Laan, L. Et Al. (2025) . "CUL3-related neurodevelopmental disorder: Clinical phenotype of 20 new individuals and identification of a potential phenotype-associated episignature." HUMAN GENETICS AND GENOMICS ADVANCES , vol.6, no.1.

@article{article, author={Liselot van der Laan Et Al. }, title={CUL3-related neurodevelopmental disorder: Clinical phenotype of 20 new individuals and identification of a potential phenotype-associated episignature}, journal={HUMAN GENETICS AND GENOMICS ADVANCES}, year=2025}