Susgun, S. Et Al. 2024. Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3). Human Mutation , vol.2024 .

Susgun, S., Ben-Mahmoud, A., Rüschendorf, F., Ku, B., Hussain, S. I., Schulz, S., ... Puk, O.(2024). Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3). Human Mutation , vol.2024.

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 , vol.2024, 2024

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 , vol.2024, 2024

Susgun, S. Et Al. (2024) . "Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3)." Human Mutation , vol.2024.

@article{article, author={Seda Susgun Et Al. }, title={Macrocephaly and Digital Anomalies Expand the Phenotypic Spectrum of PGAP2 Variants in Hyperphosphatasia with Impaired Intellectual Development Syndrome 3 (HPMRS3)}, journal={Human Mutation}, year=2024}