A novel mutation in the mutations in the methyl-CpG-binding protein 2 (MECP2) gene in a Chinese patient with typical Rett syndrome and subsequent prenatal diagnosis (vol 45, pg 806, 2018)

Ma D. Y.; Liu G.; Luo C. Y.; Liu A.; Zhang J. J.; Hu P.; Cheng J.; Wang Y. G.; Jiang T.; Xu Z. F.

首页> 外文期刊>Clinical and experimental obstetrics and gynecology >A novel mutation in the mutations in the methyl-CpG-binding protein 2 (MECP2) gene in a Chinese patient with typical Rett syndrome and subsequent prenatal diagnosis (vol 45, pg 806, 2018)

【24h】

A novel mutation in the mutations in the methyl-CpG-binding protein 2 (MECP2) gene in a Chinese patient with typical Rett syndrome and subsequent prenatal diagnosis (vol 45, pg 806, 2018)

机译：具有典型RETT综合征和后期产前诊断的中国患者中甲基-CPG结合蛋白2（MECP2）基因突变中的一种新突变（Vol 45，PG 806,2018）

获取原文

获取原文并翻译 | 示例

掌桥外文数据库（机构版） >>

开具论文收录证明 >>

文献代查 >>

页面导航

著录项
相似文献
相关主题

著录项

来源
《Clinical and experimental obstetrics and gynecology》 |2019年第1期|共1页
作者
Ma D. Y.; Liu G.; Luo C. Y.; Liu A.; Zhang J. J.; Hu P.; Cheng J.; Wang Y. G.; Jiang T.; Xu Z. F.;
展开▼
作者单位

展开▼
收录信息
原文格式 PDF
正文语种 eng
中图分类妇产科学;
关键词

相似文献

外文文献
中文文献
专利

1. A novel mutation in the mutations in the methyl-CpG-binding protein 2 (MECP2) gene in a Chinese patient with typical Rett syndrome and subsequent prenatal diagnosis (vol 45, pg 806, 2018) [J] . Ma D. Y., Liu G., Luo C. Y., Clinical and experimental obstetrics and gynecology . 2019,第1期

机译：具有典型RETT综合征和后期产前诊断的中国患者中甲基-CPG结合蛋白2（MECP2）基因突变中的一种新突变（Vol 45，PG 806,2018）
2. Methyl-CpG binding protein 2 gene (MECP2) variations in Japanese patients with Rett syndrome: pathological mutations and polymorphisms. [J] . Fukuda T, Yamashita Y, Nagamitsu S, Brain & Development . 2005,第3期

机译：日本雷特综合征患者的甲基-CpG结合蛋白2基因（MECP2）变异：病理突变和多态性。
3. Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome (letter) [J] . Obata K, Matsuishi T, Yamashita Y, Journal of Medical Genetics . 2000,第8期

机译：Rett综合征患者的甲基CpG结合蛋白2基因（MECP2）突变分析（字母）
4. GENE LOCATION AND MUTATION DETECTION IN A LARGE CHINESE FAMILY WITH SEDC AND MOLECULAR PRENATAL DIAGNOSIS OF SEDC [C] . Xin-Yi Xia, Ying-Xia Cui, Bing Yao, International Forum on Progress on Post-Genome Technologies(5'IFPT); 20070910-11; Suzhou(CN) . 2007

机译：SEDC和SEDC分子前诊断的中国大家庭的基因定位和突变检测
5. A study on two chromatin-related factors: Analysis of MeCP2 and mutations linked to Rett syndrome identification of co-factors for the insulator protein CTCF [D] . Yusufzai, Timur M. 2004

机译：两种与染色质相关的因子的研究：MeCP2分析和与Rett综合征相关的突变鉴定绝缘子蛋白CTCF的辅助因子
6. Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome [O] . K OBATA, T MATSUISHI, Y YAMASHITA, 2000

机译：Rett综合征患者甲基CpG结合蛋白2基因（MECP2）的突变分析
7. Mutation analysis of the methyl-CpG binding protein 2 gene (MECP2) in patients with Rett syndrome [O] . OBATA, K, MATSUISHI, T, YAMASHITA, Y, 2000

机译：Rett综合征患者甲基CpG结合蛋白2基因（MECP2）的突变分析

A novel mutation in the mutations in the methyl-CpG-binding protein 2 (MECP2) gene in a Chinese patient with typical Rett syndrome and subsequent prenatal diagnosis (vol 45, pg 806, 2018)

著录项

相似文献

相关主题

期刊订阅