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40篇 您的检索式:期刊名="Hum Genel"
    题名 作者 年代 出处 被引量
1A genome-wide study of com- mon SNPs and CNVs in cognitive performance in the CANTAB bat- tery 显示文摘Need AC Attix DK McEvoy JM 2009Hum Mol Genel2009,18,:1
2The genetic of psoriasis:a complex disorder of the skin and immune system显示文摘Nlalerao J Bowcock AM 1998Hum Mol Genel1998,7,10:1
3Association of the insulin-receptor variant Met-985 with hyperglycemia and non-insulin-dependent diabetes mellitus in the Netherlands: a population-based study显示文摘HART LM STOLK RP HEINE RJ 1996AM J Hum Genel1996,59,5:1
4Mutational hot spot in the DSPP gene causing dentinagenesis imperfecta type I显示文摘Kim J W Hu J C Lee J L 2005Hum Genel2005,116,3:1
5An inducible null mulanl murine model of Nijmegen breakage syndrome proves the essenlial funclion f NBS1 in chromosomal slabilily and cell viabilily显示文摘Demuth 1 Fralpar PO Hildebrand G 2004Hum MoI Genel2004,13,20:1
6Calalog of 238 variations among six human genes encoding solute carriers (hSI,Cs) in the Japanese populalion显示文摘Saito S lida A Sekine A 2002J Hum Genel2002,47,11:1
7Refined geographic distribution of the oriental ALDH2*504Lys (nee 487Lys)variant显示文摘LI HUI BORINSKAYA S YOSHIMURA K 2009Ann Hum GeneL2009,73,3:1
8Anhilrotic ectolermal dysplasin(EDA)protein expressed in MCF-7 cells associated with cell membrane and induces rounding显示文摘Ezer S Schlessinger D Srivastava A 1997Hum Mol Genel1997,6,9:1
9Spectrum of FOX12 gene mutations in blepharoph im osis-ptosis-eplcanthus inversus (BPES) families demonstrates a genotype-phenotype correlation显示文摘DE BAERE E DIXON M I SMALL K W 2001Hum Mol Genel2001,15,10:1
10Haplotypes of the human apoprotein AI-CI- II-AIV gene cluster in coronary atherosclerosis 显示文摘Ferns GA Gahon DJ 1986Hum Genel1986,73,3:1
11Linkage of autosomal recessive lamellar ichthyosis to chromosome 14q 显示文摘Russell LJ DiGiovanna JJ Hashern N 1994Am J Hum Genel1994,55,6:1
12BRCAlmRNA expression levels as an indicator of chemoresistance in lung cancer显示文摘Taron M Rosell R Felip E 2004Hum Mol Genel2004,13,:1
13Proteam PTEN: form and function显示文摘Waite KA Eng C 2002Am J Hum Genel2002,70,:1
14DNA typing and genetic mapping with trimeric and tetrameric tanders repeats显示文摘Edwards A Civitello A Hammond HA 1991Am J Hum Genel1991,49,4:1
15Linkage mapping of be- nign familial infantile convulsion to chromsomel9q 显示文摘Guipponi M Rivier F Vigevano F 1997Hum Mol Genel1997,6,3:1
16Parkin protects mitochondrial genome integrity and supports mitochondrial DNA repair显示文摘Rothfuss O Fischer H Hasegawa T 2009Hum Mol Genel2009,18,20:1
17The human serum paraoxonase polymorphism:dentification of phenotypes by the response to salts显示文摘Echerson HW 1983Am J Hum Genel1983,35,:1
18Familial infantile convulsion and paroxysmal choreothromeric region of human chrosome 16显示文摘Szepetowski P Rochette J Berqium P 1997Am J Hum Genel1997,61,:1
19A new locus for autosomal dominant dilated cardiomyopathy identified on chromosome 6q12-q16 显示文摘Sylvius N Tesson F Gayet C 2001Am J Hum Genel2001,68,:1
20Association warfarin dose with genes involved in its action and metabolism显示文摘Wadelius M Chen LY Eriksson N 2007Hum Genel2007,121,3:1
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