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40篇 您的检索式：作者名="Hoischen"

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	题名	作者	年代	出处	被引量
1	Marginal adaptation of all-ceramic crowns on implant abutments显示文摘	Att W Hoischen T Gerds T		0，，04：	1
2	De novo muta- tions of SETBP1 cause Schinzel-Giedion syndrome 显示文摘	Hoischen A van Bon BWM Gilissen C	2010	Nature genetics2010，42，6：	1
3	ST AT1 mutations in autosomal dominant chronic mucocutaneous candidiasis显示文摘	van de Veerdonk FL Plantinga TS Hoischen A	2011	N Engl J Med2011，365，1：	1
4	DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation 显示文摘	Engels H Brockschmidt A Hoischen A	2007	Neurology2007，68，10：	1
5	Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta显示文摘	Becker J Semler O Gilissen C Li Y Bolz HJ Giunta C Bergmann C Rohrbach M Koerber F Zimmermann K de Vries P Wirth B Schoenau E Wollnik B Veltman JA Hoischen A Netzer C		0，，：	1
6	ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vascu- lature显示文摘	Collin RW Nikopoulos K Dona M Gilissen C Hoischen A Boonstra FN		Proc NaU Acad Sci USA0，110，24：	1
7	Polymer-stabilized blue phases: promising me- sophases for a new generation of liquid crystal displays显示文摘	NORDENDORF G HOISCHEN A SCHMIDTKE J	2014	Polymers for Advanced Technologies2014，25，11：	1
8	Hysteresis and memory factor of the Kerr effect in bluephases显示文摘	NORDENDORF G LORENZ A HOISCHEN A	2013	Journal of Applied Physics2013，114，17：	1
9	De novo mutations of SETBP1 cause Schinzel-Giedion syndrome显示文摘	Hoischen A van Bon BW Gilissen C	2010	Nat Genet2010，42，：	1
10	The Ca2+ sensitizers CGP48506 and EMD 57033,but not the Na+ channel modulator BDF 9148,prolong contractile twitch in guinea pig cardiomyocyte显示文摘	Hoischen S Zobel C	2001	Z Kardiol2001，90，4：	1
11	Membrane alteration is necessary but not sufficient for effective glutamate secretion in Corynebacterium glutam- icum显示文摘	HOISCHEN C KRAMER R	1990	J Baeteriol1990，172，6：	1
12	DNA microarry analysis identifies candidate regions and genes in unexplained medtal retardation显示文摘	Engels H Brackschmidt A Hoischen A	2007	Neurology2007，68，10：	1
13	De novo mutations of SETBP1 cause Schinzel-Giedion syndrome显示文摘	Hoischen A van Bon BW Gilissen C	2010	Nat Genet2010，42，：	1
14	Frequent loss of chromosome 9,homozygous CDKN2A/p14(ARF)/CDKN2B deletion and low TSC1 mRNA expression in pleomorphic xanthoastrocytomas显示文摘	WEBER R G HOISCHEN A EHRLER M		0，，07：	1
15	DNA microarray analysis indentifies candidate regions and genes in unexplained mental retardation显示文摘	Engles H Brockschmidt A Hoischen A	2007	Neurology2007，68，：	1
16	De novo mutations of SETBP1 cause schinzel giedion syndrome显示文摘	Hoischen A van Bon BW Gilissen C	2010	Nat Genet2010，42，6：	1
17	Gene identification in the congenital disorders of glycosylation type I by whole-exome sequencing显示文摘	Timal S Hoischen A Lehle L	2012	Hum Mol Genet2012，21，19：	1
18	Next-generation sequencing of a 40 Mb linkage interval reveals TSPAN12 mutations in patients with familial exudative vitreoretinopathy显示文摘	Nikopoulos K Gilissen C Hoischen A van N ouhuys CE Boonstra FN Blokland EA	2010	AmJ Hum Genet2010，86，2：	1
19	Novel bacterial mem brane surface display system using cell wall-less L-forms of Proteus mirabilis and Escheriehia coli显示文摘	Hoischen C Fritsche C Gumpert J	2002	Appled and Environmental Mi- crobiology2002，68，2：	1
20	Massively parallel se- quencing of ataxia genes after array-based enrichment 显示文摘	Hoischen A Gilissen C Arts P	2010	Hum Murat2010，31，4：	1

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