维普期刊资源整合服务平台（V6.5）

维普中文期刊产品整合服务

16篇 您的检索式：作者名="MAW MA"

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	Prelingual deafness:high prevalence of a 30 delG mutation in the connexin 26 gene 显示文摘	Denoyelle F Weil D Maw MA	1997	Hum Mol Genet1997，6，：	1
	2	Prelingual deafness:high prevalence of a 30delG mutation in the connexin 26 gene显示文摘	Denoyelle F Weil D Maw MA	1997	Hum Mol genet1997，6，：	1
	3	Modeling nutrient flows in the food chain of China 显示文摘	MA L MAW Q VELTHOF G L	2010	Journal of Environmen- tal Quality2010，39，：	1
	4	A frame shift mutation in prominin (mouse)-like 1 causes human retinal degeneration显示文摘	Maw MA Corbeil D Koch J	2000	Hum Mol Genet2000，9，1：	1
	5	Fenton degradation of organic pollutants in the presence of low-molecular-weight organic acids: cooperative effect of quinone and visible light显示文摘	MA J H MAW H SONG W J CHEN C C TANG Y L ZHAO J C HUANG Y P XU Y M ZANG L	2006	Environ Sci Technol2006，40，：	1
	6	Prelingual deafness:high prevalence of a 30delG mutation in the connexin 26 gene显示文摘	Denoyelle F Weil D Maw MA	1997	Hum Mol Genet1997，6，：	1
	7	Pre lingual deafness: high prevalence of a 30deiG mutation in the connexin 26 gene 显示文摘	Denoyelle F Weil D Maw MA	1997	Hum Mol Genet1997，6，：	1
	8	Prelingual deafness:high prevalence of a 30delG mutation in the connexin 26 gene显示文摘	Denoyelle F Weil D Maw MA	1997	Hum Mol Genet1997，6，12：	1
	9	A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration显示文摘	Maw MA Corbeil D Koch J	2000	Hum Genet2000，9，1：	1
	10	Mutation of the gene encoding cellular retinaldehyde-binding protein in autosomal recessive retinitis pigmentosa 显示文摘	MAW MA KENNEDY B KNIGHT A	1997	Nat Genet1997，17，2：	1
	11	Mutation of the gene encoding cellular retinal dehyde-binding protein in autosomal recessive retinitis pigmentosa 显示文摘	Maw MA Kennedy B Knight A Bridges R Roth KE Mard EJ	1997	Nat Genet1997，17，2：	1
	12	Fenton degradation of organic compounds promoted by dyes under visible irradiation 显示文摘	MA J H SONG W J CHEN C C MAW H ZHAO J C TANG Y L	2005	Environ Sci Technol2005，39，：	1
	13	Prelingual deafness:high prevalence of a 30delG mutation in the connexin 26 gene显示文摘	Denoyelle F Weil D Maw MA		0，，：	1
	14	Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene显示文摘	Denoyelle F Weil D Maw MA	1997	Hum Mol Genet1997，6，：	1
	15	A franeshilt mutation in prominin(mouse)-like 1 cause human retinal degeneration显示文摘	MAW MA CORBEIL D KOCH J	2000	Hum Mol Gene2000，9，1：	1
	16	Prelingual deafness: high preval ence of a 30delG mutation in the connexin 26 gene显示文摘	Denoyelle F Weil D Maw MA	1997	Hum Mol Genet1997，6，：	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

goolge学术搜索-维普

网站首页 | 关于我们 | 联系我们 | 产品服务 | 客服中心 | 广告服务 | 版权声明 | 网站联盟 | 友情链接 | 售卡网点

版权所有© 渝B2-20050021-1　渝公网安备 50019002500403号　违法和不良信息举报中心

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