CONGENITAL NEPHROTIC SYNDROME: A NOVEL NON-PATHOGENIC INTRAGENIC DELETION OF WT1 WITH DEVELOPMENT OF WILMS TUMOUR: C.[643-6C > A];[(=)]

Harkins Victoria; Maxwell Heather; Ramage Ian

首页> 外文期刊>Pediatric nephrology: journal of the International Pediatric Nephrology Association >CONGENITAL NEPHROTIC SYNDROME: A NOVEL NON-PATHOGENIC INTRAGENIC DELETION OF WT1 WITH DEVELOPMENT OF WILMS TUMOUR: C.[643-6C > A];[(=)]

【24h】

CONGENITAL NEPHROTIC SYNDROME: A NOVEL NON-PATHOGENIC INTRAGENIC DELETION OF WT1 WITH DEVELOPMENT OF WILMS TUMOUR: C.[643-6C > A];[(=)]

机译：先天性肾病综合征：WT1的一种新的非致病性腺体缺失，WT1肿瘤的发育：C. [643-6C>]; [（=）]

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 >>

页面导航

著录项
相似文献
相关主题

著录项

来源
《Pediatric nephrology: journal of the International Pediatric Nephrology Association》 |2017年第9期|共2页
作者
Harkins Victoria; Maxwell Heather; Ramage Ian;
展开▼
作者单位

Nhs Greater Glasgow &

Clyde Glasgow Lanark Scotland;

Nhs Greater Glasgow &

Clyde Glasgow Lanark Scotland;

Nhs Greater Glasgow &

Clyde Glasgow Lanark Scotland;

展开▼
收录信息
原文格式 PDF
正文语种 eng
中图分类儿科学;
关键词
入库时间 2022-08-20 06:02:47

相似文献

外文文献
中文文献
专利

1. CONGENITAL NEPHROTIC SYNDROME: A NOVEL NON-PATHOGENIC INTRAGENIC DELETION OF WT1 WITH DEVELOPMENT OF WILMS TUMOUR: C.[643-6C > A];[(=)] [J] . Harkins Victoria, Maxwell Heather, Ramage Ian Pediatric nephrology: journal of the International Pediatric Nephrology Association . 2017,第9期

机译：先天性肾病综合征：WT1的一种新的非致病性腺体缺失，WT1肿瘤的发育：C. [643-6C>]; [（=）]
2. Broad and unexpected phenotypic expression in Greek children with steroid-resistant nephrotic syndrome due to mutations in the Wilms' tumor 1 (WT1) gene. [J] . Megremis S, Mitsioni A, Fylaktou I, European journal of pediatrics . 2011,第12期

机译：由于Wilms肿瘤1（WT1）基因的突变，在患有类固醇抵抗性肾病综合征的希腊儿童中出现了广泛且出乎意料的表型表达。
3. Broad and unexpected phenotypic expression in Greek children with steroid-resistant nephrotic syndrome due to mutations in the Wilms’ tumor 1 (WT1) gene [J] . Spyridon Megremis, Andromachi Mitsioni, Irene Fylaktou, European Journal of Pediatrics . 2011,第12期

机译：由于Wilms肿瘤1（WT1）基因突变，在患有类固醇抵抗性肾病综合征的希腊儿童中出现了广泛而出乎意料的表型表达
4. Pancreatic malformations as seen in congenital syndromes — Developmental perspective with an alternative view [C] . Jianhua Li, Yueyang Teng, Shouliang Qi, IEEE International Conference on Information and Automation . 2016

机译：先天性综合征中所见的胰腺畸形—发育观点和其他观点
5. Development of a clinical leukemia vaccine using dendritic cells loaded with the Wilms' tumor (WT1) gene product [D] . Van Driessche, Ann. 2011

机译：使用载有威尔姆斯肿瘤（WT1）基因产物的树突状细胞开发临床白血病疫苗
6. Evidence for WT1 as a Wilms tumor (WT) gene: intragenic germinal deletion in bilateral WT. [O] . V Huff, H Miwa, D A Haber, 1991

机译：WT1为Wilms肿瘤（WT）基因的证据：双侧WT中的基因内生发缺失。
7. WT1 splice site mutation in a 46,XX female with minimal-change nephrotic syndrome and Wilms ’ tumour [O] . Chantal Loirat, Jean Luc André, Jacqueline Champigneulle, 2015

机译：在具有微小变化的肾病综合征和肾母细胞瘤的46，XX女性中，WT1剪接位点突变

CONGENITAL NEPHROTIC SYNDROME: A NOVEL NON-PATHOGENIC INTRAGENIC DELETION OF WT1 WITH DEVELOPMENT OF WILMS TUMOUR: C.[643-6C > A];[(=)]

著录项

相似文献

相关主题

期刊订阅