Asif, M. Et Al. 2022. De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway. Human Genetics and Genomics Advances , vol.3, no.3 .

Asif, M., Kaygusuz, E., Shinawi, M., Nickelsen, A., Hsieh, T., Wagle, P., ... Budde, B. S.(2022). De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway. Human Genetics and Genomics Advances , vol.3, no.3.

Asif, Maria Et Al. "De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway," Human Genetics and Genomics Advances , vol.3, no.3, 2022

Asif, Maria Et Al. "De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway." Human Genetics and Genomics Advances , vol.3, no.3, 2022

Asif, M. Et Al. (2022) . "De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway." Human Genetics and Genomics Advances , vol.3, no.3.

@article{article, author={Maria Asif Et Al. }, title={De novo variants of CSNK2B cause a new intellectual disability-craniodigital syndrome by disrupting the canonical Wnt signaling pathway}, journal={Human Genetics and Genomics Advances}, year=2022}