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28篇 您的检索式：作者名="Sutcliffe JS"

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	题名	作者	年代	出处	被引量
1	Comparing Alternative Con- ceptualizations of Functional Diversity in Management Teams:Process and Performance Effects显示文摘	Bunderson JS Sutcliffe KM	2002	Academy of Management Journal2002，45，5：	1
2	Identification of a gene (FMR- 1) containing a CGG repeat coincident with a breakpoint duster region exhibiting length variation in fragile X syndrome显示文摘	Verkerk AJ Pieretti M Sutcliffe JS	1991	Cell1991，65，：	1
3	Identification of a gene (FMR-1) containing a CGG repeat coincident with a break point cluster region exhibiting length variation in fragile X syndrome显示文摘	Verkerk AJ Pieretti M Sutcliffe JS	1991	Cell1991，349，：	1
4	Identi fication of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome显示文摘	Verkerk AJMH Pieretti M Sutcliffe JS	1991	Cell1991，65，：	1
5	Tissue specific expres- sion of FMR - 1 provides eidence for a functional role in fraglie X syndrome显示文摘	Hinods HL Ashley CT Sutcliffe JS	1993	Nature Genet1993，3，1：	1
6	Identification of a gene(FMR- 1 )containing a CGG repeat coincident with a breskpoint cluster region exhibiting length variation in fragile X syndrome显示文摘	Verkerk AJ Pieretti M Sutcliffe JS	1991	Cell1991，65，5：	1
7	Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors 显示文摘	Sutcliffe JS Delahanty RJ Prasad HC	2005	Am J Hum Genet2005，77，2：	1
8	Influence of gender on working and spatial memory in the novel object recognition task in the rat显示文摘	Sutcliffe JS Marshall KM Neill JC		0，，1：	1
9	Identification of a gene ( FMR - 1 ) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in Fragile X syndrome显示文摘	Verkerk AJ Pieretti M Sutcliffe JS	1991	Cell1991，65，5：	1
10	Neuronally-expr-essed necdin gene: an imprinted candidate gene in Prader-Willi syndrome显示文摘	Han M Christian SL	1997	Lancet1997，350，：	1
11	Identification of a gene(FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome显示文摘	Verkerk A J Pieretti M Sutcliffe JS	1991	Cell1991，65，：	1
12	Contribution ofSHANK3 mutations to autism spectrum disorder显示文摘	Moessner R Marshall CR Sutcliffe JS	2007	Am J HumGenet2007，81，6：	1
13	Contribution of SHANK3 mutations to autism spectrum disorder 显示文摘	Moessner R Marshall CR Sutcliffe JS	2007	Am J Hum Genet2007，81，6：	1
14	Enhanced activity of human serotonin transporter variants associated with autism 显示文摘	Prasad HC Steiner JA Sutcliffe JS	2009	Philos T Roy Soc B2009，364，1514：	1
15	Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder显示文摘	Campbell DB Li C Sutcliffe JS	2008	Autism Res2008，1，3：	1
16	Identification of agene (FMR- 1) containing a CGG repeat coincident with abreakpoint cluster region exhibiting length variation in Frag-ile X syndrome显示文摘	Verkerk AJ Pieretti M Sutcliffe JS ef al	1991	Cell1991，65，：	1
17	Influence of gender on working and spatial memory in the novel object recognition task in the rat 显示文摘	Sutcliffe JS Marshall KM Neill JC	2007	Behav Brain Res2007，177，：	1
18	ldentification of a gene (FMR-I) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome 显示文摘	Verkerk AJ Pieretti M Sutcliffe JS	1991	Cell1991，65，5：	1
19	Contri- bution of SHANK3 mutations to autism spectrum disorder显示文摘	Moessner R Marshall CR Sutcliffe JS	2007	Am J Hum Genet2007，81，6：	1
20	Identification of a gene ( FMR1 ) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome 显示文摘	Verkerk AJMH Pieretti M Sutcliffe JS	1991	Cell1991，65，5：	1

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