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22篇 您的检索式：期刊名="HumanGenetic"

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	题名	作者	年代	出处	被引量
1	TheManagedHeart:TheStructuralAnalysisoftheStressor-strainRelationshipand Customer Orientation Among Emotional LaborWorkersin Korean Hotels 显示文摘	LeeG Kim TT ShinSH etal	2013	Journal of HumanGenetics2013，54，3：	1
2	Replication of the association between a chromosome 9p21 polymorphism and coronary artery disease in Japanese and Korean populations 显示文摘	HinoharaK NakajimaT Takahashi M	2008	J HumanGenet2008，53，4：	1
3	Hypergonadotropic ovarian failure associated with an inheritedmutation of human bone morphogenetic protein -15 (BMP15) gene 显示文摘	Di Pasquale E Beck-Peccoz P Persani L	2004	American journal of humangenetics2004，75，1：	1
4	Comprehensive resequence analysis of a 136 kbregion of human chromosome 8q24 associated withprostate and colon cancers 显示文摘	YEAGER M XIAO N Q HAYES R B	2008	HumanGenetics2008，124，2：	1
5	Gene ontologyanalysis of GWA study data sets provides insights into the bi-ology of bipolar disorder显示文摘	HOLMANS P GREEN E K PAHWA J S	2009	The American Journal of HumanGenetics2009，85，1：	1
6	BeckwithWiedemann syndrome显示文摘	Rosanna Weksberg Cheryl Shuman J Bruce Beckwith	2010	European Journal of HumanGenetics2010，18，：	1
7	Characterization of mutations in patients with autoimmunepolyglandular syndrome type 1 (APS1) 显示文摘	Wang CY Davoodi Semiromi A Huang W	1998	HumanGenetics1998，103，：	1
8	Protein mapping by combined isoelectric focusing and electrophoresis of mouse tissue: a novel approach to testing for induced point mutations in mammals显示文摘	Klose J	1975	Humangenetic1975，26，：	1
9	The genetic load of a human population due to cytostatic agents显示文摘	Vogel F Jager P	1969	Humangenetic1969，7，：	1
10	A silent mutation induces exon skipping in the phenylal-anine hydroxylase gene in phenylketonuria显示文摘	Hung-Kun Chao Kwang-Jen Hsiao Tsung-Sheng Su	2001	HumanGenetic2001，108，：	1
11	3rd international meeting onsingle nucleotide polymorphism and complex genome analysis:SNPs:“some notable progress”显示文摘	White P S Kwok P Y Oefner P	2001	European Journal of HumanGenetics2001，9，：	1
12	Deletions in chromosome 4 differentially associated with the development of cervical Cancer : evidence of slit2 as a candidate tumor suppressor gene显示文摘	Sing RK lndra D Mitra S	2007	HumanGenetics2007，122，：	1
13	Evidence for a founder mutation causing DFNA5 hearing loss in East Asians显示文摘	PARK H J CHO H J BAEK J I	2010	J HumanGenet2010，55，：	1
14	A quantitative -trait locus on ehromosome6p influences different aspects of developmental dyslexia显示文摘	Fisher SE MarlowAJ Lamb J	1999	American Journal of HumanGenetics1999，64，1：	1
15	Construction of agenetic linkage maps in man using restriction fragmentlength polymorphisms显示文摘	Botstein D White RL Skolnick M	1980	The American Journal of HumanGenetics1980，32，3：	1
16	Loss-of-function mutation in the dioxygenase-encoding FTOgene causes severe growth retardation and multiplemalformations 显示文摘	BOISSEL S REISH O PROULX K	2009	The American Journal of HumanGenetics2009，85，1：	1
17	A genome-Wide scan for quantitative trait loci for obesity phenotypes显示文摘	Deng Hone-Wen	2002	The American Journal of HumanGenetics2002，70，：	1
18	A comprehensive analysis of commoncopy-number variations in the human genome 显示文摘	Wong K K deLeeuw R J Dosanjh N S	2007	American Journal of HumanGenetics2007，80，：	1
19	Familial progres- sive sensorineural deafness is mainly due to the mtD- NA A1555G mutation and is enhanced by treatment of aminoglycosides显示文摘	Estivill X Govea N Barcel6 E	1998	American Journal of HumanGenetics1998，62，1：	1
20	TEtiopathogenesis of arrhythmogenic right ventricular cardiomyopathy显示文摘	Dokuparti M V N Pamuru P R Thakka B	2005	Journal of HumanGenetics2005，50，8：	1

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