A Novel PAX4 Mutation in a Japanese Patient with Maturity-Onset Diabetes of the Young von Jo, Wakako, Endo, Machiko, Ishizu, Katura, Nakamura, Akie, Tajima, Toshihiro

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Elevated Free Thyroxine Levels Detected by a Neonatal Screening System von TAJIMA, Toshihiro, JO, Wakako, FUJIKURA, Kaori, FUKUSHI, Masaru, FUJIEDA, Kenji

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Molecular analysis of the GATA3 gene in five Japanese patients with HDR syndrome von Nakamura, Akie, Fujiwara, Fumie, Hasegawa, Yukihiro, Ishizu, Katsura, Mabe, Akiyo, Nakagawa, Hiroyasu, Nagasaki, Keisuke, Jo, Wakako, Tajima, Toshihiro

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Congenital Hypothyroidism Caused by a PAX8 Gene Mutation Manifested as Sodium/Iodide Symporter Gene Defect von Jo, Wakako, Ishizu, Katsura, Fujieda, Kenji, Tajima, Toshihiro

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A Case of Novel Mutation of HNF1B in Maturity-onset Diabetes of the Young Type 5 (MODY5) von Jo, Wakako, Sano, Hitomi, Sudo, Akira, Matsunami, Yukiko, Kawamura, Nobuaki, Tajima, Toshihiro

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Development of Endometrial Carcinoma in a Patient with Leprechaunism (Donohue Syndrome) von Jo, Wakako, Sudo, Satoko, Nakamura, Akie, Endo, Daisuke, Konno, Yosuke, Ishizu, Katsura, Tajima, Toshihiro

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A Novel Mutation of the Glucokinase Gene in Maturity-onset Diabetes of the Young Type 2 (MODY2) von Jo, Wakako, Fujieda, Kenji, Tajima, Toshihiro

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Case Study of a 15-Year-old Boy with McCune-Albright Syndrome Combined with Pituitary Gigantism: Effect of Octreotide-long Acting Release (LAR) and Cabergoline Therapy von TAJIMA, Toshihiro, TSUBAKI, Junko, ISHIZU, Katsura, JO, Wakako, ISHI, Nobuaki, FUJIEDA, Kenji

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A Novel Splicing Mutation of the GNAS Gene in a Patient with Pseudohypoparathyroidism Ia von Nakamura, Akie, Hostubo, Tomoyuki, Jo, Wakako, Ishizu, Katsura, Tajima, Toshihiro

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Elevated Free Thyroxine Levels Detected by a Neonatal Screening System von Tajima, Toshihiro, Jo, Wakako, Fujikura, Kaori, Fukushi, Masaru, Fujieda, Kenji

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Development of Endometrial Carcinoma in a Patient with Leprechaunism (Donohue Syndrome) von Wakako Jo, Satoko Sudo, Akie Nakamura, Daisuke Endo, Yosuke Konno, Katsura Ishizu, Toshihiro Tajima

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Molecular analysis of the GATA3 gene in five Japanese patients with HDR syndrome von Akie Nakamura, Fumie Fujiwara, Yukihiro Hasegawa, Katsura Ishizu, Akiyo Mabe, Hiroyasu Nakagawa, Keisuke Nagasaki, Wakako Jo, Toshihiro Tajima

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A Novel Splicing Mutation of the GNAS Gene in a Patient with Pseudohypoparathyroidism Ia von Akie Nakamura, Tomoyuki Hostubo, Wakako Jo, Katsura Ishizu, Toshihiro Tajima

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Case Study of a 15-Year-old Boy with McCune-Albright Syndrome Combined with Pituitary Gigantism: Effect of Octreotide-long Acting Release (LAR) and Cabergoline Therapy von TOSHIHIRO TAJIMA, JUNKO TSUBAKI, KATSURA ISHIZU, WAKAKO JO, NOBUAKI ISHI, KENJI FUJIEDA

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P13-2-7 Congenital hypothyroidism caused by a PAX8 gene mutation manifested as sodium/iodide symporter gene defect von Toshihiro Tajima, Wakako Jo, Kenji Fujieda

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P-08 ANALYSIS OF THE HESX1 AND THE LHX4 GENE IN JAPANESE PATIENTS WITH COMBINED PITUITARY HORMONE DEFICIENCY (CPHD) von Ishizu, Katsura, Jo, Wakako, Fujiwara, Fumie, Tsubaki, Junko, Fujieda, Kenji, Tajima, Toshihiro

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A Novel Mutation of the Glucokinase Gene in Maturity-onset Diabetes of the Young Type 2 (MODY2) von Jo, Wakako, Fujieda, Kenji, Tajima, Toshihiro

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A Novel Splicing Mutation of the GNAS Gene in a Patient with Pseudohypoparathyroidism Ia von Nakamura, Akie, Hostubo, Tomoyuki, Jo, Wakako, Ishizu, Katsura, Tajima, Toshihiro

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Development of endometrial carcinoma in a patient with leprechaunism (donohue syndrome) von Jo, Wakako, Sudo, Satoko, Nakamura, Akie, Endo, Daisuke, Konno, Yosuke, Ishizu, Katsura, Tajima, Toshihiro

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Congenital Hypothyroidism Caused by a PAX8 Gene Mutation Manifested as Sodium/Iodide Symporter Gene Defect von Jo, Wakako, Ishizu, Katsura, Fujieda, Kenji, Tajima, Toshihiro

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