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17篇 您的检索式：作者名="Devi RR"

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		题名	作者	年代	出处	被引量
	1	Crystallin gene mutation in Indian families with inherited pediatric cataract显示文摘	Devi RR Yah W Vijayalakshmi P	2008	Mol Vis2008，14，：	1
	2	Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcomea显示文摘	Devi RR Vijayalakshmi P	2006	Mol Vision2006，12，：	1
	3	Bioethanol production from rice straw: An overview显示文摘	Binod P Sindhu R Singhania RR Vikram S Devi L Nagalakshmi S Kurien N Sukumaran RK Pandey A	2010	Bioresource Technology2010，101，13：	1
	4	Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea显示文摘	Devi RR Vijayalakshmi P	2006	Mol Vision2006，12，：	1
	5	Students' perspectives regarding an ideal PBL case 显示文摘	Devi V Abraham RR Pallath V	2011	Med Teach2011，33，2：	1
	6	Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea显示文摘	Devi RR Vijayalakshmi P	2006	Mol Vis2006，12，：	1
	7	Crystallin gene mutations in Indian families with inherited pediatric cataract 显示文摘	Devi RR Yao W Vijayalakshmi P	2008	Mol Vis2008，14，：	1
	8	Novel mutations in GJA3 associated with autosomal dominant congenital cataract in the Indian population显示文摘	Devi RR Reena C Vijayalakshmi P	2005	Mol Vis2005，11，：	1
	9	Plasma homocysteine levels correlated to interactions between folate status and meth- ylene tetrahydrofolate reductase gene mutation in women with unexplained recurrent pregnancy loss 显示文摘	Kumar KS Naushad SE Devi RR	2003	J Obstet Gynecol2003，23，1：	1
	10	Fostering research skillsin undergraduate medical students through mentored students pro-jects: example from an Indian medical school 显示文摘	Devi V Abraham RR Adiga A	2010	KathmanduUniv Med J (KUMj)2010，8，31：	1
	11	Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea 显示文摘	Devi RR Vijayalakshrai P	2006	Mol Vis2006，12，：	1
	12	Crystallin gene mutations in Indian families with inherited pediatric cataract显示文摘	Devi RR Yao WL Vijaylakshmi P Sergeev YV Sundaresan P Hejtmancik JF	2008	Mol Vis2008，14，：	1
	13	The HITRAN molecular spectroscopic database:edition of 2000 including updates through 2001显示文摘	Rothman LS Barbe A Chris Benner D Brown LR Camy-Peyret C Carleer MR Chance K Clerbaux C Dana V Devi VM Fayt A Flaud J-M Gamache RR Goldman A Jacquemart D Jucks KW Lafferty WJ Mandin J-Y Massie ST Nemtchinov V Newnham DA Perrin A Rinsland CP Schroeder J Smith KM Smith MAH Tang K Toth RA Vander Auwera J Varanasi P Yoshino K	2003	JQSRT2003，82，：	1
	14	Novel mutations in GJA3 as-sociated with autosomal dominant congenital cataract in the Indianpopulation显示文摘	Devi RR Reena C Vijayalakshmi P	2005	Mol Vis2005，11，：	1
	15	Crystallin gene mutations in Indian families with inherited pediatric cataract显示文摘	Devi RR Yao W Vijayalakshmi P	2008	Mol Vis2008，14，：	1
	16	Students' perspectives regarding an ideal PBL case 显示文摘	Devi V Abraham RR Pallath V	2011	Med Teach2011，33，2：	1
	17	Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea 显示文摘	Devi RR Vijayalakshmi P	2006	Mol Vis2006，12，：	1

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