Tsutsumi, M., Yokoi, S., Miya, F., Miyata, M., Kato, M., Okamoto, N., . . . Kurahashi, H. (2016). Novel compound heterozygous variants in PLK4 identified in a patient with autosomal recessive microcephaly and chorioretinopathy. Eur J Hum Genet.
Styl ChicagoTsutsumi, Makiko, et al. "Novel Compound Heterozygous Variants in PLK4 Identified in a Patient With Autosomal Recessive Microcephaly and Chorioretinopathy." Eur J Hum Genet 2016.
Citace podle MLATsutsumi, Makiko, et al. "Novel Compound Heterozygous Variants in PLK4 Identified in a Patient With Autosomal Recessive Microcephaly and Chorioretinopathy." Eur J Hum Genet 2016.
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