TÜRKYILMAZ, A. And Sager, S. G. 2022. Two New Cases of Primary Microcephaly with Neuronal Migration Defect Caused by Truncating Mutations in the ASPM Gene. MOLECULAR SYNDROMOLOGY , vol.13, no.1 , 56-63.

TÜRKYILMAZ, A., & Sager, S. G., (2022). Two New Cases of Primary Microcephaly with Neuronal Migration Defect Caused by Truncating Mutations in the ASPM Gene. MOLECULAR SYNDROMOLOGY , vol.13, no.1, 56-63.

TÜRKYILMAZ, AYBERK, And Safiye Gunes Sager. "Two New Cases of Primary Microcephaly with Neuronal Migration Defect Caused by Truncating Mutations in the ASPM Gene," MOLECULAR SYNDROMOLOGY , vol.13, no.1, 56-63, 2022

TÜRKYILMAZ, AYBERK And Sager, Safiye G. . "Two New Cases of Primary Microcephaly with Neuronal Migration Defect Caused by Truncating Mutations in the ASPM Gene." MOLECULAR SYNDROMOLOGY , vol.13, no.1, pp.56-63, 2022

TÜRKYILMAZ, A. And Sager, S. G. (2022) . "Two New Cases of Primary Microcephaly with Neuronal Migration Defect Caused by Truncating Mutations in the ASPM Gene." MOLECULAR SYNDROMOLOGY , vol.13, no.1, pp.56-63.

@article{article, author={AYBERK TÜRKYILMAZ And author={Safiye Gunes Sager}, title={Two New Cases of Primary Microcephaly with Neuronal Migration Defect Caused by Truncating Mutations in the ASPM Gene}, journal={MOLECULAR SYNDROMOLOGY}, year=2022, pages={56-63} }