APA
Takasawa K., Igarashi M., Ono M., Takemoto A., Takada S., Yamataka A., Ogata T., Morio T., Fukami M. & Kashimada K. (20181022). Phenotypic Variation in 46,XX Disorders of Sex Development due to the NR5A1 p.R92W Variant: A Sibling Case Report and Literature Review. : Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation.
Chicago
Takasawa Kei, Igarashi Maki, Ono Makoto, Takemoto Akira, Takada Shuji, Yamataka Atsuyuki, Ogata Tsutomu, Morio Tomohiro, Fukami Maki and Kashimada Kenichi. 20181022. Phenotypic Variation in 46,XX Disorders of Sex Development due to the NR5A1 p.R92W Variant: A Sibling Case Report and Literature Review. : Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation.
Harvard
Takasawa K., Igarashi M., Ono M., Takemoto A., Takada S., Yamataka A., Ogata T., Morio T., Fukami M. and Kashimada K. (20181022). Phenotypic Variation in 46,XX Disorders of Sex Development due to the NR5A1 p.R92W Variant: A Sibling Case Report and Literature Review. : Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation.
MLA
Takasawa Kei, Igarashi Maki, Ono Makoto, Takemoto Akira, Takada Shuji, Yamataka Atsuyuki, Ogata Tsutomu, Morio Tomohiro, Fukami Maki and Kashimada Kenichi. Phenotypic Variation in 46,XX Disorders of Sex Development due to the NR5A1 p.R92W Variant: A Sibling Case Report and Literature Review. : Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation. 20181022.