Murata, Y., Kurosaka, H., Ohata, Y., Aikawa, T., Takahata, S., Fujii, K., . . . Yamashiro, T. (2019). A novel PTCH1 mutation in basal cell nevus syndrome with rare craniofacial features. Hum Genome Var.
Παραπομπή Chicago StyleMurata, Yuka, et al. "A Novel PTCH1 Mutation in Basal Cell Nevus Syndrome With Rare Craniofacial Features." Hum Genome Var 2019.
Παραπομπή MLAMurata, Yuka, et al. "A Novel PTCH1 Mutation in Basal Cell Nevus Syndrome With Rare Craniofacial Features." Hum Genome Var 2019.
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