1. Acroscyphodysplasia as a phenotypic variation of pseudohypoparathyroidism and acrodysostosis type 2. Issue 10 (10th July 2014) Authors: Mitsui, Toshikatsu; Kim, Ok‐Hwa; Hall, Christine M.; Offiah, Amaka; Johnson, Diana; Jin, Dong‐Kyu; Toh, Teck‐Hock; Soneda, Shun; Keino, Dai; Matsubayashi, Shohei; Ishii, Tomohiro; Nishimura, Gen; Hasegawa, Tomonobu Journal: American journal of medical genetics Issue: Volume 164:Issue 10(2014.) Page Start: 2529 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Acroscyphodysplasia as a phenotypic variation of pseudohypoparathyroidism and acrodysostosis type 2. Issue 10 (10th July 2014) Authors: Mitsui, Toshikatsu; Kim, Ok‐Hwa; Hall, Christine M.; Offiah, Amaka; Johnson, Diana; Jin, Dong‐Kyu; Toh, Teck‐Hock; Soneda, Shun; Keino, Dai; Matsubayashi, Shohei; Ishii, Tomohiro; Nishimura, Gen; Hasegawa, Tomonobu Journal: American journal of medical genetics Issue: Volume 164:Issue 10(2014.) Page Start: 2529 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Retrospective study of the renal function using estimated glomerular filtration rate and congenital anomalies of the kidney‐urinary tract in pediatric Turner syndrome. (4th August 2020) Authors: Izumita, Yukie; Nishigaki, Satsuki; Satoh, Mari; Takubo, Noriyuki; Numakura, Chikahiko; Takahashi, Ikuko; Soneda, Shun; Abe, Yoshifusa; Kamasaki, Hotaka; Ohtsu, Yoshiaki; Igaki, Junko; Hasegawa, Yukihiro; Nagasaki, Keisuke Journal: Congenital anomalies Issue: Volume 60:Number 6(2020) Page Start: 175 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗