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22篇 您的检索式：作者名="Bouteiller D"

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	题名	作者	年代	出处	被引量
1	Familial cortical myoclonic tremor with epilepsy:the third locus (FCMTE3) maps to 5p显示文摘	Depienne C Magnin E Bouteiller D	2010	Neurology2010，74，24：	1
2	Familial cortical my-oclonic tremor with epilepsy : the third locus (FCMTE3 ) maps to5p显示文摘	Depienne C Magnin E Bouteiller D	2010	Neurology2010，74，24：	1
3	Familial cortical myoclonic tremor with epilepsy: the third locus (FCMTE3) maps to 5p显示文摘	Depienne C Magnin E Bouteiller D	2010	Neurology2010，4，24：	1
4	Configurable three-wavelength Raman fiber laser for Raman amplification and dynamic gain flattening显示文摘	MERMELSTEIN M D HEADLEY C BOUTEILLER J C	2001	IEEE Photon Technol Lett2001，13，12：	1
5	Sporadic infantile ep- ileptic encephalopathy caused by mutations in PCDH19 resem- bles Dravet syndrome but mainly affects females 显示文摘	Depienne C Bouteiller D Keren B	2009	PLoS Genet2009，5，10：	1
6	Familial cortical myoclonic tremor with epilepsy: the third locus (FCMTE3) maps to 5p显示文摘	Depienne C Magnin E Bouteiller D	2010	Neurology2010，74，24：	1
7	Sporadic infantile ep- ileptic encephalopathy caused by mutations in PCDH19 resem- bles Dravet syndrome but mainly affects females 显示文摘	Depienne C Bouteiller D Keren B	2009	PLoS Genet2009，5，10：	1
8	Mutations and dele- tions in PCDH19 account for various familial or isolated epilepsies in females 显示文摘	Depienne C Trouillard O Bouteiller D	2011	Hum Mutat2011，32，1：	1
9	HLA-G remains a mystery显示文摘	Bainbridge D Ellis S Bouteiller P	2001	Trends in Immunology2001，22，10：	1
10	Familial cortical my?oclonic tremor with epilepsy: the third locus (FCMTE3) maps to 5p显示文摘	Depienne C Magnin E Bouteiller D	2010	Neurology2010，74，24：	1
11	Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females显示文摘	Depienne C Bouteiller D Keren B	2009	PLoS Genet2009，5，2：	1
12	Visualization of chromatin distribution in living PTO cells by Hoecbst 33342 fluores- cent staining显示文摘	Gregoire M Hernandez-Verdun D Bouteille M	1984	Exp Cell Res1984，152，1：	1
13	Familial cortical myoclonie tremor with epilepsy : the third locus ( FCMTE3 ) maps to 5p显示文摘	Depienne C Magnin E Bouteiller D	2010	Neurology2010，74，24：	1
14	Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females显示文摘	DEPIENE C BOUTEILLER D KEREN B	2009	PLoS Gene2009，5，10：	1
15	Mutations and deletions in PCDH19 account for various familial or isolated epilepsies in females显示文摘	Depienne C Trouillard O Bouteiller D		0，，01：	1
16	Familial cortical myoclonic tremor with epilepsy: the third locus (FCMTE3) maps to 5p显示文摘	Depienne C Magnin E Bouteiller D	2010	Neurology2010，74，：	1
17	Familial cortical myoclon- ic tremor with epilepsy: the third locus (FCMTE3) maps to 5p显示文摘	Depienne C Magnin E Bouteiller D	2010	Neurology2010，74，24：	1
18	Sporadic infantileepileptic encephalopathy caused by mutations in PCDH19 re- sembles Dravet syndrome but mainly affects females 显示文摘	Depienne C Bouteiller D Keren g	2009	PLoS Genet2009，5，2：	1
19	Mutations and De-letions in PCDH19 Account forVarious Familial or Isolated Epilep-sies in Females显示文摘	Depienne C Trouillard 0 Bouteiller D	2011	Hum Mutat2011，32，1：	1
20	Mutations and de-letions in PCDH19 account for various familiar or isolated epi-lepsies in females显示文摘	Depienne C Trouillard 0 Bouteiller D	2011	Hum Mutat2011，32，1：	1

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