|
English
|
正體中文
|
简体中文
|
全文筆數/總筆數 : 29490/55136 (53%)
造訪人次 : 1994277
線上人數 : 390
|
|
|
資料載入中.....
|
請使用永久網址來引用或連結此文件:
http://ir.cmu.edu.tw/ir/handle/310903500/29134
|
題名: | Glutathione S-transferase M1 gene null genotype and gastric cancer risk in Taiwan |
作者: | Lai, KC;Chen, WC;Tsai, FJ;Li, SY;Chou, MC;Jeng, LB |
貢獻者: | 附設醫院外科部;China Med Univ Hosp, Dept Surg, Taichung, Taiwan;China Med Univ Hosp, Dept Med Genet, Taichung, Taiwan;Chung Shan Med Univ, Grad Inst Med, Taichung, Taiwan |
日期: | 2005 |
上傳時間: | 2010-09-24 14:23:18 (UTC+8) |
出版者: | H G E UPDATE MEDICAL PUBLISHING S A |
摘要: | A girl presented with a phenotype including neonatal hypotonia, psychomotor retardation, mental retardation, short stature, and facial dys-morphism. She demonstrated common features of both 14q31-qter duplication and terminal 14q deletion. She had undergone surgery for patent ductus arteriosus and pyloric stenosis in infancy. Her karyotype was 46,XX,der(14) dup(14)(q32.3 q31.3)del(14)(q32.3). Molecular cytogenetic analysis showed a paternally derived 14q31.3-q32.3 duplication and a terminal 14q deletion and led to the correlations between a particular genotype and phenotype. This is the first description of a deletion and inverted duplication of 14q and adds 14q to the growing list of the inverted duplication associated with a terminal deletion. (c) 2005 Wiley-Liss, Inc. |
關聯: | HEPATO-GASTROENTEROLOGY 52(66):1916-1919 |
顯示於類別: | [台中附設醫院] 期刊論文
|
在CMUR中所有的資料項目都受到原著作權保護.
|