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

13篇 您的检索式：作者名="Meitinger T"

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	Genome-wide association studies of atrial fibrillation: past, present, and future 显示文摘	Sinner MF Ellinor PT Meitinger T	2011	Cardiovasc Res2011，89，4：	1
	2	Associations between calcium and vitamin D supplement use as well as their serum concentrations and subclinical cardiovascular disease phenotypes显示文摘	Inke Thiele Jakob Linseisen Christa Meisinger Sigrid Schwab Cornelia Huth Annette Peters Siegfried Perz Thomas Meitinger Florian Kronenberg Claudia Lamina Joachim Thiery Wolfgang Koenig Wolfgang Rathmann Stefan K??b Cornelia Then Jochen Seissler Barbara T	2015	Atherosclerosis2015，，2：	1
	3	Pantothenate kinase?associated neurodegeneration显示文摘	Hartig MB Prokisch H Meitinger T	2012	CUff Drug Targets2012，13，9：	1
	4	Adolescent growth:genes,hormones and the peer group显示文摘	Hermanussen M Meitinger T Veldhuis JD	2014	Pediatr Endocrinol Rev2014，11，3：	1
	5	STAT3 single-nucleotide polymorpbisms and STAT3mutations associated with hyper-IgE syndrome are not responsible for increased serum IgE serum levels in asthma families显示文摘	Wjst M Lichtner P Meitinger T		0，，03：	1
	6	Diabetes insipidus,diabetes mellitus,optic atrophy and deafness (DIDMOAD) caused by mu-tations in a novel gene (wolframin) coding for a predicted trans-membrane protein显示文摘	Strom TM Hortnagel K Hofmann S Gekeler F Scharfe C Rabl W Gerbitz KD Meitinger T		0，，：	1
	7	Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate显示文摘	Mangold E Ludwig KU Birnbaum S Baluardo C Ferrian M Herms S Reutter H de Assis NA Chawa TA Mattheisen M Steffens M Barth S Kluck N Paul A Becker J Lauster C Schmidt G Braumann B Scheer M Reich RH Hemprich A Potzsch S Blaumeiser B Moebus S Krawczak M Schreiber S Meitinger T Wichmann HE Steegers-Theunissen RP Kramer FJ Cichon S Propping P Wienker TF Knapp M Rubini M Mossey PA Hoffmann P Nothen MM	2010	Nat Genet2010，42，：	1
	8	A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures显示文摘	K Schlachter U Gruber-Sedlmayr E Stogmann M Lausecker C Hotzy J Balzar E Schuh C Baumgartner J C. Mueller T Illig H E. Wichmann P Lichtner T Meitinger T M. Strom A Zimprich F Zimprich	2009	Neurology2009，，11：	1
	9	An L-type calcium-channel gene mutated in incomplete X-linked congenital stationary night blindness 显示文摘	Strom TM Nyakatura G Apfelstedt-Sylla E Hellebrand H Lorenz B Weber BH Wutz K Gutwillinger N Ruther K Drescher B Sauer C Zrenner E Meitinger T R osenthal A Meindl A	1998	Nat Genet1998，19，3：	1
	10	Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk显示文摘	Rivera A Fisher SA Fritsche LG Keilhauer CN Lichmer P Meitinger T	2005	Hum Mol Genet2005，14，21：	1
	11	Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins显示文摘	Meindl A Berger W Meitinger T	1992	Nat Genet1992，2，2：	1
	12	A splice site variant in the sodium channel gene SCN1A confers risk of febrile seizures显示文摘	K Schlachter U Gruber-Sedlmayr E Stogmann M Lausecker C Hotzy J Balzar E Schuh C Baumgartner J C. Mueller T Illig H E. Wichmann P Lichtner T Meitinger T M. Strom A Zimprich F Zimprich	2009	Neurology2009，，11：	1
	13	Age-related macular degeneration and functional promoter and coding variants of the apolipoprotein E gene显示文摘	Fritsche LG Freitag-Wolf S Bettecken T Meitinger T Keilhauer CN Krawczak M		0，，07：	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