Origin and mechanism of formation of 45,X/47,XX,+21 mosaicism in a fetus von Harada, Naoki, Abe, Kyohko, Nishimura, Tomoko, Sasaki, Kiminori, Ishikawa, Mutsuo, Fujimoto, Masahiro, Matsumoto, Tadashi, Niikawa, Norio

Volltext

Disomic homozygosity in 21-trisomic cells: a mechanism responsible for transient myeloproliferative syndrome von ABE, K, KAJII, T, NIIKAWA, N

Volltext

Isolation of cosmid clone corresponding to an inv(21) breakpoint of a patient with transient abnormal myelopoiesis von OHTA, T, NAKANO, M, NIIKAWA, N, TSUJITA, T, ABE, K, OSOEGAWA, K, YAMAGATA, T, YOSHIURA, K.-I, JINNO, Y, SOEDA, E, NAKAMURA, Y

Volltext

Parental origin and mechanism of formation of polysomy X: an XXXXX case and four XXXXY cases determined with RFLPs von Deng, H X, Abe, K, Kondo, I, Tsukahara, M, Inagaki, H, Hamada, I, Fukushima, Y, Niikawa, N

Volltext

Possible mapping of the gene for transient myeloproliferative syndrome at 21q11.2 von NIIKAWA, N, HAN-XIANG DENG, KUWANO, A, KAJII, T, ABE, K, HARADA, N, OKADA, T, TSUCHIYA, H, AKABOSHI, I, MATSUDA, I, FUKUSHIMA, Y, KANEKO, Y

Volltext

Molecular study of the Prader-Willi syndrome: Deletion, RFLP, and phenotype analyses of 50 patients von Hamabe, Jun-Ichi, Fukushima, Yoshimitsu, Harada, Naoki, Abe, Kyohko, Matsuo, Nobutake, Nagai, Toshiro, Yoshioka, Akira, Tonoki, Hidefumi, Tsukino, Ryuichi, Niikawa, Norio

Volltext

Satellited chromosome 9 in a boy with multiple anomalies von Harada, Naoki, Abe, Kyohko, Kondoh, Tatsuro, Hirota, Tetsuya, Niikawa, Norio

Volltext

Monosomy for 21pter-q21: Case report and assignment of a DNA clone (Fr8-77) to the deleted segment von Abe, Kyohko, Deng, Han-Xiang, Harada, Naoki, Yoshiura, Koh-ichiro, Oh-hira, Takahiko, Nikawa, Norio

Volltext

Complex chromosome rearrangements: Report of three patients von Kamei, Tsutomu, Lee-Okimoto, Sei, Yamada, Yasushi, Abe, Kyohko, Mastumoto, Tadashi, Niikawa, Norio

Volltext

A molecular deletion study with Southern hybridization on typical Prader-Willi syndrome (PWS) patients with various chromosome abnormalities involving 15q11-12 and on an atypical P... von Kamei, Tsutomu, Hamabe, Jun-ichi, Matsumoto, Tadashi, Abe, Kyohko, Harada, Naoki, Ishikiriyama, Satoshi, Hasegawa, Tomoko, Miyazaki, Kiyoshi, Mizuno, Seiji, Narahara, Kouji, Yukizane, Shigenori, Niikawa, Norio

Volltext

Waardenburg syndrome type I in a child with de novo inversion (2)(q35q37.3) von Ishikiriyama, Satoshi, Tonoki, Hidefumi, Shibuya, Yoshitaka, Chin, Shinki, Harada, Naoki, Abe, Kyohko, Niikawa, Norio

Volltext

Diagnosis of four chromosome abnormalities of unknown origin by chromosome microdissection and subsequent reverse and forward painting von de Albuquerque Coêlho, Katia-Édni F., Egashira, Masayuki, Kato, Rumiko, Fujimoto, Masahiro, Matsumoto, Naomichi, Rerkamnuaychoke, Budsaba, Abe, Kyohko, Harada, Naoki, Ohashi, Hirofumi, Fukushima, Yoshimitsu, Niikawa, Norio

Volltext

A case of successful treatment of type II hepatorenal syndrome with transjugular intrahepatic portosystemic shunt using carbon dioxide as a contrast medium von TANIMURA, Kyohko, KANAZAWA, Hidenori, YOSHIMOTO, Hitoshi, KOIZUMI, Nobuhito, MAMIYA, Yasutaka, OSADA, Yuuji, KURODA, Hajime, SAKAMOTO, Tyouitsu, KOBAYASHI, Masafumi, SHIMODA, Takaya, ARAI, Hirotaka, SUZUKI, Hideyuki, ABE, Takehiko

Volltext

CO2を造影剤に用いたTIPSにより改善を得たII型肝腎症候群の1例 von 谷村, 恭子, 金沢, 秀典, 吉本, 均, 小泉, 信人, 間宮, 康貴, 長田, 祐二, 黒田, 肇, 坂本, 長逸, 小林, 正文, 下田, 隆也, 新井, 弘隆, 鈴木, 秀行, 阿部, 毅彦

Volltext