维普期刊资源整合服务平台（V6.5）

29篇 您的检索式：作者名="Morizio"

选中清除导出查看参考文献查看引证文献引用追踪共2页首页上一页第1页下一页末页 /2 跳转

	题名	作者	年代	出处	被引量
1	Two multichannel integrated circuits for neural recording and signal processing显示文摘	Obeid I Morizio JC Moxon KA	2003	IEEE Transactions on Biomedical Engnineering2003，50，2：	1
2	Enhanced phase noise modeling of fractional-N frequency synthesizers显示文摘	Himanshu Arora Nikolaus Klemmer James C Morizio	2005	IEEE Transactions on Circuits and Systems-Ⅰ: Regular Papers2005，52，2：	1
3	Assignment of TACSTD1 (alias TROP1,M4S1) to human chromosome 2p21 and refinement of mapping of TACSTD2 (alias TROP2,M1S1) to human chromosome lp32 by in situ hybridization 显示文摘	Calabrese G Crescenzi C Morizio E	2001	Cytogenet Cell Genet2001，92，12：	1
4	Deletion of the SHOX gene in patients with short stature of unknown cause 显示文摘	Morizio E Stuppial L Gatta V	2003	Am J Hum Genet2003，119，3：	1
5	A LCOS Microdisplay Driver with Frame Buffer Pixels显示文摘	Sangrok Lee Morizio J C Johnson K M	2003	Information Sciences2003，149，：	1
6	Novel frame buffer pixel circuits for liquid-crystal-on-silicon microdisplays显示文摘	Sangrok Lee Morizio J C Johnson K M	2004	IEEE Journal of Solid-State Circuits2004，39，1：	1
7	Deletion of the SHOX gene in patients with short stature of unknown cause显示文摘	Morizio E Stuppia L Gatta V	2003	Am J Med Genet2003，119，3：	1
8	A LCOS microdisplay driver with frame buffer pixels显示文摘	LEE S MORIZIO J C JOHNSON K M	2003	Information Sciences2003，149，1：	1
9	Identification of 14 Rare Marker Chromosomes and Derivatives by Spectral Karyo typing in Prenatal and Postnatal Diagnosis显示文摘	Guanciali-Franchi P Calabrese G Morizio E	2004	Am J Med Genet A2004，127，2：	1
10	Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol显示文摘	Antonucci I Iezzi I Morizio E	2009	BMC Biotechnol2009，9，：	1
11	Novel frame buffer pixel circuits for liquid-crystal-on-silicon microdisplays 显示文摘	Lee S Morizio J C Johnson K M	2004	IEEE Solid-State Circuits2004，39，1：	1
12	Deletion of the SHOX gene in patients with short stature of unknown cause显示文摘	Morizio E Stuppia L Gatta V	2003	Am J Med Genet2003，119，3：	1
13	Identification and characterization of different SHOX gene deletions in patients with Leri–Weill dyschondrosteosys by MLPA assay显示文摘	Valentina Gatta Ivana Antonucci Elisena Morizio Chiara Palka Rita Fischetto Vahe Mokini Stefano Tumini Giuseppe Calabrese Liborio Stuppia	2007	Journal of Human Genetics2007，，1：	1
14	Enhanced phase noise modeling of fractional-N frequency synthesizers显示文摘	ARORA H KLEMMER N MORIZIO J C	2005	IEEE Trans Circ Syst2005，52，2：	1
15	Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis 显示文摘	Guanciali - Franehi P Calabrese G Morizio E	2004	Am J Med Genet2004，127，2：	1
16	En- hanced phase noise modeling of fractional-N frequency synthesizers 显示文摘	ARORA H KLEMMER N MORIZIO J C	2005	IEEE Transactions on Circuits and Systems: I2005，52，2：	1
17	A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11显示文摘	Liborio Stuppia Valentina Gatta Giuseppe Calabrese Paolo Guanciali Franchi Elisena Morizio Cristina Bombieri Rita Mingarelli Vincenzo Sforza Giovanni Frajese Raffaele Tenaglia G. Palka	1998	Human Genetics1998，，5：	1
18	Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol显示文摘	Antonucci I Iezzi I Morizio E		0，，：	1
19	Assignment of TACSTD1 (alias TROP1,M4S1) to human chromosome 2p21 and refinement of mapping of TACSTD2 (alias TROP2,M1S1) to human chromosome 1 p32 by in situ hybridization显示文摘	Calabrese G Crescenzi C Morizio E		0，，1：	1
20	Assignment of TACSTD1 (alias TROP1,M4S1)to human chromosome 2p21 and refinement of mapping of TACSTD2 (alias TROP2,M1S1) to human chromosome lp32 by in situ hybridization显示文摘	Calabrese G Crescenzi C Morizio E Palka G Guerra E Alberti S	2001	Cytogenet Cell Genet2001，92，12：	1

返回顶部每页显示：

共2页首页上一页第1页下一页末页 /2 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