APA

Hasegawa K., Higuchi Y., Yamashita M. & Tanaka H. (20150214). Japanese familial case with metaphyseal dysplasia, Schmid Type caused by the p.T555P mutation in the COL10A1 gene. : Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Chicago

Hasegawa Kosei, Higuchi Yosuke, Yamashita Miho and Tanaka Hiroyuki. 20150214. Japanese familial case with metaphyseal dysplasia, Schmid Type caused by the p.T555P mutation in the COL10A1 gene. : Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

Harvard

Hasegawa K., Higuchi Y., Yamashita M. and Tanaka H. (20150214). Japanese familial case with metaphyseal dysplasia, Schmid Type caused by the p.T555P mutation in the COL10A1 gene. : Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology.

MLA

Hasegawa Kosei, Higuchi Yosuke, Yamashita Miho and Tanaka Hiroyuki. Japanese familial case with metaphyseal dysplasia, Schmid Type caused by the p.T555P mutation in the COL10A1 gene. : Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology. 20150214.