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

18篇 您的检索式：作者名="Laccone"

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	Dysmorphic syndrome of hereditary neuralgic amyotrophy associated with a SEP'19 gene mu- tation-a family study 显示文摘	Laccone F Hannibal M C Neesen J	2008	Clin Genet2008，74，3：	1
	2	Usefulness of lasartan on the size of the ascending aorta in an unselected cohort of children,adolescents,and young adults with Marfan syndrome显示文摘	PEES C LACCONE F HAGL M	2013	Am J Cardiol2013，112，9：	1
	3	MECP2 gene nucleotide changes and their pathogenicity in males: proceed with caution显示文摘	Laccone F Zoll B Huppke P	2002	J Med Geuet2002，39，8：	1
	4	MECP2 mutations in sporadic cases of Rett syndrome are almost exclusively of paternal origin显示文摘	Trappe R Laccone F Cobilanschi J	2001	Am J Hum Genet2001，68，5：	1
	5	SCA2 trinucleotide expansion in German SCA patients显示文摘	Olaf Riess Franco A. Laccone Suzana Gispert Ludger Sch?ls Christine Zühlke Ana Maria Menezes Vieira-Saecker Susanne Herlt Karl Wessel J?rg T. Epplen Bernhard H.F. Weber Friedmar Kreuz Soheyla Chahrokh-Zadeh Alfons Meindl Astrid Lunkes Jorge Aguiar Milan M	1997	Neurogenetics1997，，1：	1
	6	MECP2 gene nucleotide changes and their pathogenicity in males:proceed with caution显示文摘	Laccone F Zoll B Huppke P	2002	J Med Genet2002，39，8：	1
	7	MECP2 gene nucleotide changes and their pathogenicity in males: proceed with caution 显示文摘	Laccone F Zoll B Huppke P	2002	J Med Genet2002，39，8：	1
	8	Association of Jacobsen syndrome and bipolar alfective disorder in a patient with a de novo 11q terminal deletion显示文摘	Bohm D Hoffmann K Laccone F	2006	Am J Med Genet2006，140，4：	1
	9	Hip dysplasia and spinal osteochondritis (Scheuermannts disease) in a girl with type Ⅱ manifesting collagenopathy 显示文摘	AL KA LACCONE F KARNER C	2013	Orthopade2013，42，11：	1
	10	Large deletions of the MECP2 gene detected by gene dosage analysis in patients with Rett syndrome显示文摘	Laccone F Junemann I Whatley S	2004	Hum Murat2004，23，3：	1
	11	Mutation and polymorphisms in the human methyl CpG-binding protein MECP2显示文摘	Miltenberger-miltenyi G Laccone F	2003	Human Mutat2003，22，10：	1
	12	Quatitative diffusion-weighted MR imaging in the differential diagnosis of breast lesion 显示文摘	Marinic lacconic Giannelli Metal	2007	Eur Radiol2007，17，10：	1
	13	MECP2 gene nucleotide changes and their pathogenicity in males:proceed with caution显示文摘	Laccone F Zoll B Huppke P	2002	J Med Genet2002，39，8：	1
	14	The spectrum of phenotypes in females with Rett Syndrome显示文摘	Huppke P Held M Laccone F	2003	Brain Dev2003，25，3：	1
	15	Restless legs syndrome in spinocerebellar ataxia types 1, 2 and 3显示文摘	Abele M Burk K Laccone F	2001	J Neurol2001，248，：	1
	16	Mutations and polymorphisms in the human methyl CpG-binding protein MECP2显示文摘	Miltenberger-Miltenyi G Laccone F		0，，：	1
	17	Trinucleotide repeat expansion in SCA17/TBP in white patients with Huntington's disease-like phenotype显示文摘	Bauer P Laccone F Rolfs A	2004	J Med Genet2004，41，：	1
	18	Large deletions of the MECP2 gene detected by gene dosage analysis in patients with Rett syndrome显示文摘	Laccone F Junemann I Whatley S	2004	Hum Mutat2004，23，：	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