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Clinical Pediatric Endocrinology : Case Reports and Clinical Investigations : Official Journal of the Japanese Society for Pediatric Endocrinology|January 15, 2021
X-linked mental retardation and severe short stature with a novel mutation of the <i>KDM5C</i> geneFumika Kawano-Matsuda, Tomoki Maeda, Tadashi Kaname, et al.
Neuro Endocrinology Letters|August 1, 2017
Central hypoadrenocorticism associated with Rathke's cleft cystFumika Kawano, Tomoyo Itonaga, Masanori Inoue, et al.
CEN Case Reports|November 7, 2020
A case of HDR syndrome coexisting with tetralogy of Fallot, with a novel GATA3 mutation, which manifested as a renal abscessMayo Ikeuchi, Kyoko Kiyota, Tomoyo Itonaga, et al.
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