Naseer, M. I., Rasool, M., Abdulkareem, A. A., Chaudhary, A. G., Zaidi, S. K., & Al-Qahtani, M. H. (2019). Novel compound heterozygous mutations in WDR62 gene leading to developmental delay and Primary Microcephaly in Saudi Family. Pak J Med Sci.
Citação norma ChicagoNaseer, Muhammad Imran, Mahmood Rasool, Angham Abdulrahman Abdulkareem, Adeel G. Chaudhary, Syed Kashif Zaidi, and Mohammad H. Al-Qahtani. "Novel Compound Heterozygous Mutations in WDR62 Gene Leading to Developmental Delay and Primary Microcephaly in Saudi Family." Pak J Med Sci 2019.
ציטוט MLANaseer, Muhammad Imran, et al. "Novel Compound Heterozygous Mutations in WDR62 Gene Leading to Developmental Delay and Primary Microcephaly in Saudi Family." Pak J Med Sci 2019.
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