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A 26-Day-Old Japanese Girl with Aldosterone Synthase Deficiency Caused by a Novel Mutation in the CYP11B2 Gene | ESPE2014
Satomi Koyama; Tatsuo Tsuboi; Naoto Shimura; Akie Nakamura; Toshihiro Tajima; Osamu Arisaka
Published: 2014-08-28

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A Novel Mutation of wfs1 Gene in a Japanese Infant of Diabetes Mellitus, Deafness, and Congenital Cataract | ESPE2014
Shuntaro Morikawa; Akie Nakamura; Katsura Ishizu; Satoru Kumaki; Toshihiro Tajima
Published: 2014-08-28

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Safety of GH in Paediatrics: The GeNeSIS Prospective Observational Study Experience between 1999 and 2015 (NCT01088412) | ESPE2016
Werner Blum; Christopher Child; George Chrousos; Elisabeth Cummings; Cheri Deal; Tomonobu Hasegawa; Paul-Martin Holterhus; Nan J
Published: 2016-08-19

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