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52篇 您的检索式:作者名="WINDPASSINGER"
    题名 作者 年代 出处 被引量
1Precodingand loading for BLAST-like systems 显示文摘Windpassinger C Vencel T Fischer R F H 2003IEEEInternational Conference on Communications2003,,5:1
2Precoding in multi-antenna and multi-user communications显示文摘Windpassinger C Fischer R F H Vencel T 2004IEEE Transaction on Wireless Communications2004,,3:1
3Precoding in multiantenna and muhiuser communications 显示文摘Windpassinger C Fischer R F H Vencel T 2004IEEE Transactions on Wireless Communications2004,3,4:1
4Precoding in Multiantenna and Multiuser Communications显示文摘Windpassinger C Fischer R F H Vencel T 2004IEEE Trans on Wireless Commun2004,3,4:1
5General movements in genetic disorders:A first look into Cornelia de Lange syndrome显示文摘Marschik PB Soloveichick M Windpassinger C 2013Dev Neurorehabil2013,16,6:1
6Heterozygous missense mutations in BSCL2 are associ- ated with distal hereditary motor neuropathy and Sil- ver syndrome显示文摘Windpassinger C Auer-Grumbach M Irobi J 2004Nat Genet2004,36,3:1
7Lattice - reduction - aided broadcast precoding 显示文摘WINDPASSINGER C FISCHER R F H HUBER J B 2004IEEE Trans Comm2004,52,:1
8Prece- ding in multi-antenna and muhiuser communications 显示文摘WINDPASSINGER C FISCHER R F H VENCEL T 2004I EEE Trans on Wireless Communication2004,3,4:1
9CC2D2A, Encoding A coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosa显示文摘Noor A Windpassinger C Patel M 2008Am J Hum Genet2008,82,4:1
10Pre- coding in muhiantenna and multiuser communication 显示文摘WINDPASSINGER C FISCHER F H VENCEL T 2004IEEE Trans Wireless Commun2004,3,4:1
11An X-linked myopathy with postural muscle atrophy and generalized hypertrophy, termed XMPMA, is caused by mutations in FHL1 显示文摘Windpassinger C Sehoser B Straub V 2008Am J Hum Genet2008,82,:1
12Precoding in muhiantenna and multiuser communications 显示文摘WINDPASSINGER C FISCHER R F H VENCELT 2004IEEE Transactions on Communications2004,3,4:1
13查看详情显示文摘J Appel P J Windpassinger D Oblak U B Hoff N Kj(ae)rgaard and E S Polzik 0,,:1
14Lattice-reduction-aided Broadcast Precoding 显示文摘Windpassinger C Fischer R F Huber J B 2004IEEE Transactions on Communications2004,52,12:1
15An X-linked myopathy with postural muscle atrophy and generalized hypertrophy, termed XMPMA, is caused by mutations in FHL1 显示文摘Windpassinger C Schoser B Straub V 2008Am J Hum Genet2008,82,1:1
16Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome显示文摘Windpassinger C Auer-Grmnbach M Irobi J 2004Nat Genet2004,36,3:1
17Precoding in multiantenna and multiuser communications显示文摘Windpassinger C Fischer R F H Vencel T 2004IEEE Trans Wireless Commun2004,3,4:1
18Precoding in muhiantenna and multiuser communications显示文摘WINDPASSINGER C FISCHER R F H VENCEL T 0,,04:1
19Heterozygous missense mutations in BSCL2 are associated with distal hereditary motor neuropathy and Silver syndrome显示文摘Windpassinger C Auer-Grumbach M Irobi J Patel H Petek E Horl G 2004Nat Genet2004,36,:1
20Multiple-symbol differential sphere decoding 显示文摘L Lampe R Schober V Pauli C Windpassinger 2005IEEE Transactions on Communications2005,53,12:1
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