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15篇 您的检索式：作者名="RAMESAR R"

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		题名	作者	年代	出处	被引量
	1	Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldism显示文摘	Spritz RA Holmes SA Ramesar R	1992	Am J Hum Genet1992，51，5：	1
	2	Neuropsychological dysfunction in bipolar affective disorder: a critical opinion 显示文摘	Savitz J Solms M Ramesar R	2005	BipolarDisord2005，7，3：	1
	3	The molecular genetics of cognition:dopamine显示文摘	Savitz J Solms M Ramesar R		0，，：	1
	4	The importance of G protein-coupled receptor kinase 4(GRK4) in pathogenesis of salt sensitivity, salt sensitive hypertension and response to antihypertensive treatment 显示文摘	RAYNER B RAMESAR R	2015	IntJ Mol Sci2015，16，3：	1
	5	Spondyloepiphyseal dysplasia in a Cape Town family:linkage with the gene for type Ⅱ collagen (COL2A1)显示文摘	Beighton P	1992	Am J Med Genet1992，43，：	1
	6	Neuropsychological dysfunction in bipolar affective disorder: a critical opinion显示文摘	Savitz J Solms M Ramesar R	2005	Bipolar Disord2005，7，3：	1
	7	Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldism显示文摘	Spritz RA Holmes SA Ramesar R	1992	Am J Hum Genet1992，51，5：	1
	8	Autosomal dominant (Beukes) premature degenerative osteoarthropathy of the hip joint unlinker to COL2A1显示文摘	Cilliers HJ Ramesar R	1994	Am J Med Genet1994，53，：	1
	9	Mapping of the gene for cleidocranial dysplasia in the historical Cape Town (Arnold) kindred and evidence for locus homogeneity 显示文摘	Ramesar RS Greenberg J Martin R	1996	Med Genet1996，33，：	1
	10	The molecular genetics of cognition:dopamine,COMT and BDNF显示文摘	Savitz J Solms M Ramesar R	2006	Genes Brain Behav2006，5，4：	1
	11	Apoptosis-inducing signal sequence mutation in carbonic anhydrase Ⅳ identified in patients with the RP17 form of retinitis pigmentosa 显示文摘	Rebello G Ramesar R Vorster A	2004	Proc Natl Acad Sci USA2004，101，：	1
	12	Molecular genetics improves the management of hereditary non-polypsis colorectal cancer显示文摘	Ramesar RS Madden MV Felix R	2000	S Aft Med J2000，90，7：	1
	13	Apoptosis-inducing signal sequence mutation in carbonic anhydrase IV identified in patients with the RP17 form of retinitis pigmentosa显示文摘	Rebello G Ramesar R Vorster A Roberts L Ehrenreich L Oppon E	2004	Proc Natl Acad Sci USA2004，101，17：	1
	14	A mutation in the variable repeat region of the aggrecan gene (AGCI) causes a form of spondyloepiphyseal dysplasia associated with severe, premature osteoarthritis显示文摘	Gleghom L Ramesar R Beighton P	2005	Am J Hum Genet2005，77，：	1
	15	Neuropsychological dysfunction in bipolar affective disorder:a critical opinion显示文摘	Savitz J Solms M Ramesar R	2005	Bipolar Disord2005，7，：	1

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