Susgun, S., Ben-Mahmoud, A., Rüschendorf, F., Ku, B., Hussain, S. I., Schulz, S., . . . Kim, H. (2024). Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3). Human Mutation, 1-13. https://doi.org/10.1155/2024/5518289

Susgun, Seda, et al. "Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3)." Human Mutation 2024: 1-13. https://doi.org/10.1155/2024/5518289.

Susgun, Seda, et al. "Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3)." Human Mutation, 2024, pp. 1-13, https://doi.org/10.1155/2024/5518289.