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16篇 您的检索式：作者名="Rees MI"

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		题名	作者	年代	出处	被引量
	1	A two-stage genome scan for schizophrenia susceptibility genes in 196 affected sibling pairs显示文摘	Williams NM Rees MI Holmans P	1999	Hum Mol Genet1999，8，9：	1
	2	Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11(CZP3) and a novel mutation in connexin46 (GJA3) 显示文摘	Ree MI Watts P Fenton I	2000	Hum Genet2000，106，2：	1
	3	Molecular investigation of TBP allele length: a SCA17 cellular model and population study显示文摘	Reid SJ Rees MI van Roon-Mom WM	2003	Neurobiol Dis2003，13，：	1
	4	A genomewide linkage study of age at onset in schizophrenia 显示文摘	Cardno AG Holmans PA Rees MI	2001	Am J Med Genet2001，105，5：	1
	5	Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11 (CZP3) and a novel mutation in connexin 46 (GJA-3)显示文摘	Rees MI Watts P Fenton I	2000	Hum Genet2000，106，：	1
	6	An affected sib-pair study for schizophrenia on the X chromosome显示文摘	Norton N Williams NM Rees MI	1999	Am J Med Genet1999，81，：	1
	7	Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13q11(CZP3) and a novel mutation in connexin 46 (GJA3)显示文摘	Rees MI Watts P Fenton I	2000	Hum Genet2000，106，：	1
	8	The genetics of epilepsy-the past,the present and future显示文摘	Rees MI	2010	Seizure2010，1，9：	1
	9	The genetics of epilepsy-fue past, the present and future显示文摘	Rees MI	2010	Seizure2010，19，：	1
	10	Radiologic and pathologic findings of intracerebral schwannoma 显示文摘	Zagardo MT Castellani RJ Rees JH Rothman MI Zoarski GH	1998	Am J Ne uroradiol1998，19，7：	1
	11	Characterisation, mutation detection, and association analysis of alternative promoters and 5' UTRs of the human dopamine D3 receptor gene in schizophrenia 显示文摘	Anney R J Rees MI Bryan E	2002	Mol Psychiatry2002，7，5：	1
	12	Hyperekplexia associated with compound heterozygote mutations in the beta-subunit of the human inhibitory glyeine receptor (GLRB) 显示文摘	Rees MI Lewis TM Kwok JB	2002	Hum Mol Genet2002，11，7：	1
	13	Isoform heterogeneity of the human gephyrin gene (GPHN), binding domains to the glycine receptor,and mutation analysis in hyperekplexia 显示文摘	Rees MI Harvey K Ward H	2003	J Biol Chem2003，278，24：	1
	14	Further evidence of autosomal dominant congenital zonular pulverulent cataracts linked to 13qll(CZP3) and a novel mutation in connexin 46 (GJA3) 显示文摘	Rees MI Watts P Fenton I Clarke A Snell RG Owen MJ	2000	Hum Genet2000，106，2：	1
	15	A two-stage genome scan for schizophreni a susceptibility genes in 196 affected sibling pairs显示文摘	Williams NM Rees MI Holmans P	1999	Hum Mol Genet1999，8，9：	1
	16	Characterisation,mutation detection,and association analysis of alternative promoters and 5'UTRs of the human dopamine D3 receptor gene in schizophrenia显示文摘	Anney RJ Rees MI Bryan E	2002	Mol Psychiatry2002，7，5：	1

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