维普期刊资源整合服务平台（V6.5）

20篇 您的检索式：作者名="CHIOZA"

选中清除导出查看参考文献查看引证文献引用追踪共1页首页上一页第1页下一页末页 /1 跳转

	题名	作者	年代	出处	被引量
1	Linkage and mutational analysis of CLCN2 in childhood absence epilepsy显示文摘	Everett K Chioza B Aicardi J	2007	Epilepsy Res2007，75，23：	1
2	Linkage and mutational analysis of CLCN2 in childhood absence epilepsy显示文摘	Everett K Chioza B Aicardi J	2007	Epilepsy Res2007，75，23：	1
3	Linkage and mutational analysis of CLCN2 inchildhood absence epilepsy显示文摘	Everett K Chioza B Aicardi J	2007	Epilepsy Res2007，75，：	1
4	Linkage and mutation analysis of CLCN2 in childhood absence epilepsy显示文摘	Everett K Chioza B Aicardi J	2007	Epilepsy Res2007，75，23：	1
5	Mutations in all five exons of SOD-1 may cause ALS显示文摘	SHAW CE ENAYAT ZE CHIOZA BA		0，，03：	1
6	Linkage and mutational analy?sis of CLCN2 in childhood absence epilepsy显示文摘	Everett K Chioza B AicardiJ	2007	Epilepsy Res2007，75，23：	1
7	Linkage and association analysis of CACNG3 in childhood absence epilepsy 显示文摘	Everett KV Chioza B Aicardi J	2007	Eur J Hum Genet2007，15，4：	1
8	Infantile hypertrophic pyloric stenosis: evaluation of three positional candidate genes, TRPC1, TRPC5 and TRPC6, by association analysis and re-sequencing显示文摘	Kate V. Everett Barry A. Chioza Christina Georgoula Ashley Reece R. Mark Gardiner Eddie M. K. Chung	2009	Human Genetics2009，，6：	1
9	Evaluation of CACNA1H in European patients with childhood absence epilepsy显示文摘	Chioza B Everett K Aschauer H	2006	Epilepsy Res2006，69，：	1
10	Genome-wide High-Density SNP-Based Linkage Analysis of Infantile Hypertrophic Pyloric Stenosis Identifies Loci on Chromosomes 11q14-q22 and Xq23显示文摘	Kate V. Everett Barry A. Chioza Christina Georgoula Ashley Reece Francesca Capon Keith A. Parker Cathy Cord-Udy Paul McKeigue Sally Mitton Agostino Pierro Prem Puri Hannah M. Mitchison Eddie M.K. Chung R. Mark Gardiner	2008	The American Journal of Human Genetics2008，，3：	1
11	Linkage and association analysis of CACNG3 in childhood absence epilepsy 显示文摘	Everett KV Chioza B Aicardi J	2007	Eur J Hum Genet2007，15，4：	1
12	Suggestive evidence for association of two potassium channel genes with different idiopathic generalised epilepsy syndromes显示文摘	Chioza B Osei-Lah A Wilkie H	2002	Epilepsy Res2002，52，：	1
13	Suggestive evidence for association of two potassium channel genes with different idi-opathic generalised epilepsy syndromes 显示文摘	Chioza B Osei-Lah A Wilkie H	2002	Epilepsy Res2002，52，：	1
14	Genome-wide high-density SNP-based linkage analysis of infantile hypertrophic pyloric stcnosis identifies loci on chromosomes 11q14-q22 and Xq23 显示文摘	Everett KV Chioza BA Georgoula C	2008	Am J Hum Genet2008，82，3：	1
15	Evaluation of CACNA1H in European patients with childhood absence epilepsy显示文摘	Chioza B Everett K Aschauer H	2006	Epilepsy Res2006，，：	1
16	Genorne wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23- pl4显示文摘	Chioza BA Aicardi J Aschauer H	2009	Epilepsy Res2009，87，23：	1
17	Linkage and mutational analysis of CLCN2 in childhood absence epilepsy显示文摘	Everett K Chioza B Aicardi J	2007	Epilepsy Res2007，75，23：	1
18	Genome-wide high-density SNP-based linkage analysis of infantile hypertrophic pyloric stenosis identifies loci on chromosomes 11q14-q22 and Xq23显示文摘	EVERETT K V CHIOZA B A GEORGOULA C	2008	Am J Hum Genet2008，82，3：	1
19	Infantile hypertrophic pyloric stenosis:evaluation of three positional candidate genes,TRPC1,TRPC5 and TRPC6,by association analysis and re-sequencing显示文摘	EVERETT K V CHIOZA B A GEORGOULA C	2009	Hum Genet2009，126，6：	1
20	Suggestive evidence for association of twopotassium channel genes with different idiopathic generalised epilepsysyndromes显示文摘	Chioza B Osei-Lah A Wilkie H	2002	Epilepsy Res2002，52，：	1

返回顶部每页显示：

共1页首页上一页第1页下一页末页 /1 跳转

互联网出版许可证新出网证(渝)字10号全国400电话 - 免长途话费

用户提示