Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Mitsushiro Kida"'
Autor:
Akira Tonomura, Akira Tamura, Mitsushiro Kida, Shinji Karasawa, Koichi Ichimura, Eiko Arai, Yasuhito Yuasa, Kohtaro Yamamoto, Tatsuro Ikeuchi
Publikováno v:
American Journal of Medical Genetics. 44:163-167
We report on a female patient with bilateral acoustic neurinomas and other tumors in the central nervous system (neurofibromatosis type 2: NF2) and the constitutional translocation, t(4;22) (q12;q12.2). The precise identification of the translocation
Publikováno v:
The Japanese journal of human genetics. 39(4)
Distal deletion of chromosome 1q has been reported in nearly 30 patients, all being associated with a deletion ranging from the 1q42 or q43 band to 1qter region. Here, we describe a girl with 1q terminal deletion resulting from an unbalancedde novo t
Autor:
Takako Takano, Masatsune Date, Mitsushiro Kida, Yutaka Nakahori, Shintaro Hashira, Yasuko Yamanouchi, Toshiaki Abe, Shoko Kawashima, Yasuo Nakagome
Publikováno v:
Clinical genetics. 44(6)
Takano T, Yamanouchi Y, Kawashima S, Date M, Hashira S, Kida M, Abe T, Nakahori Y, Nakagome Y. 11q trisomy detected by fluorescence in situ hybridization. Clin Genet 1993: 44: 324–328. © Munksgaard, 1993 A patient with psychomotor developmental de
Publikováno v:
Cancer Genetics and Cytogenetics. 25:253-258
The patient studied was a 33-year-old female in the blastic phase of chronic myelocytic leukemia resistant to busulfan. The results of cytogenetic studies of bone marrow cells were as follows: The abnormal chromosomes were double Ph 1 ,+19,+6,+B, rin
Autor:
Mitsushiro Kida
Publikováno v:
Congenital Anomalies. 28:33-44
Some 137 patients with thalidomide embryopathy have been registered. Of them, 65 were male and 72 female. The age of patients who had a medical examination from 1976 to 1983, ranged from 7 to 22 years. The mean age was 17.0 ± 2.3 (mean ± SD) years.
Publikováno v:
Pediatrics International. 24:299-302
We described complex de novo rearrangements involving four chromosomes in a child with congenital malformations. Clinical features of this patient resembled those of cri du chat syndrome. Examinations in electroencephalography, electrocardiography, c
Autor:
Mitsushiro Kida, Mariko Uehara
Publikováno v:
Jinrui idengaku zasshi. The Japanese journal of human genetics. 31(1)
Autor:
Mariko Uehara, Mitsushiro Kida
Publikováno v:
Jinrui idengaku zasshi. The Japanese journal of human genetics. 31(1)
When cultured lymphocytes of a patient with 45,XY,t(13;18) (p11.1-2;p11.2) were treated with mitomycin C (MMC), dissociations of t(13;18) chromosomes were increased as compared with controls. Furthermore, various other anomalies in volving t(13;18),