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16篇 您的检索式：作者名="Tong SF"

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		题名	作者	年代	出处	被引量
	1	A novel missense mu- tation (P191L) in the glucose-6-phosphate translocase gene identified in a Chinese family with glycogen storage disease 1b显示文摘	Lam CW Chan KY Tong SF	2000	Hum Mutat2000，16，：	1
	2	Identification of a no- vel missense mutation (G149E) in the glucose-6-phosphate translocase gene in a Chinese family with glycogen storage disease type lb显示文摘	Lam CW Tong SF Lam YY	1999	Hum Mutat Online Report1999，，：	1
	3	Men's health:sexual dysfunction,physical,and psychological health--is there a link显示文摘	Tan HM Tong SF Ho CC		0，，03：	1
	4	Prospects for TIM3-Tar- geted Antitumor Immunotherapy显示文摘	Ngiow SF Tong MW Smyth MJ	2011	Cancer Res2011，71，65：	1
	5	Atypical presentation of dopa-responsive dystonia:generalized hypotonia and proximal weakness显示文摘	Kong CK Ko CH Tong SF	2001	Neurology2001，57，6：	1
	6	A novel missense mutation(P191L)in the glucose-6-phosphatetranslocase gene identified in a Chinese family with glycogenstorage disease 1b显示文摘	Lam CW Chan KY Tong SF Chan BY Chan YT Chan YW	2000	Hum Mutat2000，16，1：	1
	7	Nitric oxide induces oral squamous cell carcinoma cells apoptosis with p53 accrumularion显示文摘	Zhao SF Tong XY Zhu FD	2005	Oral Oncol2005，41，8：	1
	8	Aerobic oxidation of 4-tert-butyltoluene over cobalt and manganese supported hexagonalmesoporous silicas as heterogeneous catalysts显示文摘	Yu W H Zhou C H Tong D Sf	2012	J Mol Catal A:Chem2012，365，：	1
	9	Clinical efficiency and safety analysis of transcatheter interventional therapy for compound congenital cardiovascular abnormalities 显示文摘	Song ZY Shu MQ Hu HY Tong SF Ran BL Liu JP	2007	Clin Cardiol2007，30，10：	1
	10	DNA -based diagnosis of malignant osteopetrosis by whole - genome scan using a single - nucJeotide polymorphism microarray: standardization of molecular investigations of genetic diseases due to consanguinity 显示文摘	Lain CW Tong SF Wang K	2007	J Hum Genet2007，52，1：	1
	11	Polymeric micelle gene delivery of bel-xL via eye drop reduced corneal apoptosis follow- ing epithelial debridement显示文摘	TONG YC CHANG SF KAO WW	2010	J Control Release2010，147，1：	1
	12	Two novel CLN2 gene mutations in a Chinese patient with classical late-infantile neuronal ceroid lipofuscinosis显示文摘	Lam CW Poon PM Tong SF	2001	Am J Med Genet2001，99，2：	1
	13	Novel missense mu- tation (Y24H) in the SLC37A4 gene causing glycogen stor- age disease type 1b显示文摘	Yuen YP Cheng WF Tong SF	2002	Mol Genet Metab2002，77，：	1
	14	Atypical presentation of dopa-responsive dystonia:generalized hypotonia and proximal weakness显示文摘	Kong CK Ko CH Tong SF	2001	Neurology2001，57，：	1
	15	Atypical presentation of dopa-responsive dystonia: generalized hypotonia and proximal weakness显示文摘	Kong CK Ko CH Tong SF	2001	Neurology2001，57，：	1
	16	Glucocerebrosidase mutations and risk of Parkinson's disease in chinese patients显示文摘	Tan EK Tong J Chong SF	2007	Arch Neurol2007，64，7：	1

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