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17篇 您的检索式:作者名="Sebastio G"
    题名 作者 年代 出处 被引量
1Molecular analysis of aldolase B genes in hereditary fructose intol- erance 显示文摘Cross N C de Franchis R Sebastio G 1990The Lancet1990,335,8685:1
2Lysinuric protein intoler- ance: reviewing concepts on a multisystem disease 显示文摘Sebastio G Sperandeo MP Andria G 2011Am J Med Genet C Semin Med Genet2011,157,1:1
3Control of lactase in human adult-type hypolactasia and in weaning rabbits and rats 显示文摘Sebastio G Mantei N Villa M 1989Am J Hum Genet1989,45,4:1
4The molecular basis of homocystinuria due to cystathionine beta-synthase deficiency in Italian families, and report of four novel mutations显示文摘Sebastio G Sporandeo MP Panico M 1995Am J Hum Genet1995,56,4:1
5The molecular basis Of homocystinuria due to cystathionineβ- synthase deficiency in Italian families, and report of four novel mutation显示文摘Sebastio G Sperandeo MP Panico M 1995Am J Hum Genet1995,56,6:1
6The molecular basis of homocystinuria due to cystathionine β-synthase deficiency in Italian families,and report of four novel mutation显示文摘Sebastio G Sperandeo MP Panico M 1995Am J Hum Genet1995,56,6:1
7The molecular basis of homocystinuria due to cystathionine β- synthase deficiency in Italian families, and report of four novel muta'tions显示文摘Sebastio G Sperandeo MP Panico M 1995Am J Hum Genet1995,56,6:1
8Molecular analysis of aldolase B genes in hereditary fructose intolerance 显示文摘Cross N C Defranchis R Sebastio G 1990The Lancet1990,335,8685:1
9The mole- cular basis of homocystinuria due to cystathionine beta - synthase deficiency in Italian families, and report of four novel mutations 显示文摘SEBASTIO G SPERANDEO M P PANICO M 1995Am J Hum Genet1995,56,6:1
10The molecular bases of cystinuriaand lysinuric protein intolerance显示文摘Palacin M Borsani G Sebastio G 2001Curr Opin Genet Dev2001,11,3:1
11The molecular basis ofhomocystinuria due to cystathionineβ-synthase deficiency in Italianfamilies,and report of four novel mutation显示文摘Sebastio G Sperandeo MP Panico M 1995Am J Hum Genet1995,56,6:1
12Lysinuric protein in-tolerance characterized by bonemarrow abnormalities and severe clini-cal course显示文摘Parenti G Sebastio G StrisciugHo P 1995J Pediatr1995,126,2:1
13The molecular basis of homocystinuria due to cystathionine - b -synthase deficiency in italian families and report of fournovel mutations 显示文摘Sebastio G Sperandeo MP Panico M 1995Am J Hum Genet1995,56,:1
14The molecular basis of homocystinuria due to cystathionine bata-synthase deficiency in Italian families , and report of four novel mutations显示文摘Sebastio G Sperandeo MP Panico M 1995Am J Hum Genet1995,56,6:1
15The molecular basis of homocystinuria due to cystathionine β-synthase deficiency in Italian families,and report of four novel mutations显示文摘Sebastio G Sperandeo MP Panico M 1995Am J Hum Genet1995,56,:1
16The molecular basis of homocystinuria due to cystathionine β-synthase deficiency in Italian families, and report of four novel mutation 显示文摘Sebastio G Sperandeo MP Panico M 1995Am J Hum Genet1995,56,6:1
17Sequence analysis and in vivo expression show that alternative splicing of ED-B and ED-A regions of the human fibronectin gene are independent events显示文摘Paolella G Henchcliffe C Sebastio G 1988Nucleic Acids Res1988,16,8:1
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