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15308篇 您的检索式:期刊名="Hum- Mol-Genet"
    题名 作者 年代 出处 被引量
1Laryngeal and oropharyngeal cancer, and alcohol dehydrogenase 3 and glutathione S-transferase M1 polymorphisms显示文摘Coutelle C Ward PJ Fleury B Quattrocchi P Chambrin H Iron A 1997Hum Genet1997,99,3:3
2A stop-codon mutation in the human mtDNA cytochrome c oxidase I gene disrupts the functional structure of complex IV显示文摘Bruno A Martinuzzi Y Tang Y 1999Am J Hum Genet1999,65,3:2
3Linkage disequilibrium between polymorphisms in the human TNFRSF1B gene and their association with bone mass in perimenopausal women显示文摘Albagha O M E Tasker P N McGuigan F E A 2002Hum Molec Genet2002,11,:2
4Protein PTEN: Form and Function显示文摘Waite KA Eng C 2002Am J Hum Genet2002,70,4:2
5DNA polymorphism haplotypes of the human lipoprotein lipase gene: possible association with high density lipoprotein levels显示文摘HEINZMANN C KIRCHGESSNER T KWITEROVICH P O 1991Hum Genet1991,86,6:2
6DNA typing and genetic mapping with trimetric and tetrametric tandem repeats 显示文摘Edwards A Civitello A Hammond H A 1991Am J Hum Genet1991,49,4:2
7Mapping of a gene for long QT syndrome to chromosome 4q25-27显示文摘Schott JJ Charpentier F Pelter S 1995Am J Hum Genet1995,57,:1
8An extension of the admixture test for the study of genetic heterogeneity in hereditary multiple exostoses 显示文摘Legeai- Mallet L Margaritte- Jeannin P Lemdani M 1997Hum Genet1997,99,3:1
9Estimating the power of a proposed linkage study for a complex genetics trait 显示文摘BOEHNK P M 1989Am J Hum Genet1989,44,4:1
10Localization of factors controlling spermatogenesis in the nonfluorescent position of the human Y chromosome long arm显示文摘Tiepolo L Zuffardi O 1976Hum Genet1976,34,2:1
11Efficient direct chromosome analyses and enzyme determination from chorinic villi samples in the first trimester of pregnancy 显示文摘Simoni G Brambiti B Denestno C 1983Hum Genet1983,63,4:1
12A missense Glu298Asp variant in the endothelial nitric oxide synthase gene is associated with coronary spasm in the Japanese显示文摘Yoshimura M Yasue H Nakayama M 1998Hum Genet1998,103,1:1
13Limb-girdle muscular dystrophy type 2H associated with mutation in TRIM32, a putative E3-ubiquitin-ligase gene 显示文摘Frosk P Weiler T Nylen E 2002Am J Hum Genet2002,70,3:1
14Construction of a genetic linkage map in man using restriction fragment length polymorphisms 显示文摘Botstein D White RL Skolnick M 1980Am J Hum Genet1980,32,3:1
15From chromosomes to DNA, a revolution in prenatal diagnosis显示文摘Breuning MH 2005Eur J Hum Genet2005,13,5:1
16Localization of factors controlling spermatogenesis in the nonfluorescent portin of the human Y chromosome long arm 显示文摘Tiepolo L Zuffardi O 1976Hum Genet1976,34,2:1
17Methods for high-density admixture mapping of disease genes 显示文摘PATTERSON N HATrANGADI N LANE B 2004Am J of Hum Genet2004,74,:1
18A large-scale genetic association study confirms IL 12B and leads to the identification of IL23R as psoriasis-risk genes显示文摘Cargill M Schrodi S J Chang M 2007Am J Hum Genet2007,80,2:1
19Construction of a genetic linkage map in man using restriction fragment length polymorphisms 显示文摘Botstein D White R L Skolnick M 1980Am J Hum Genet1980,32,:1
20Identification of uniparental disomy foiling prenatal detection of robertsonian translocations and isochromosomes显示文摘Berend SA Horwitz J McCaskill C 2000Am J Hum Genet2000,6,:1
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