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38篇 您的检索式:作者名="kyndt F"
    题名 作者 年代 出处 被引量
1Proximal tubular dysfunction in primary Sjogren's syndrome: a clinicopathological study of 2 cases显示文摘Bridoux F Kyndt X Abou-Ayache R 2004Clin Nephrol2004,61,:1
2Novel SCNSA mutation leading either to isolated cardiac conduction defect or brugada syndrome in a large french family显示文摘Kyndt F Probst V Potet F 2001Circulation2001,104,25:1
3Cardiac conduction defects associate with mutation in SCN5A显示文摘Schott JJ Alshinawi C Kyndt F 1999(letter)Nature Genet1999,23,:1
4Cardiac conduction defects associate with mutations in SCN5A显示文摘SCHOTT J J ALSHINAWI C KYNDT F 1999Nat Genet1999,23,9:1
5Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndronm in a large French family显示文摘Kyndt F Probst V Potet F 2001Circulation2001,104,:1
6显示文摘Kyndt X Reumaux D Bridoux F 1999Am J Med1999,106,:1
7Cardiac conduction defects associate with mutations in SCN5A显示文摘 Alshinawi C Kyndt F 1999Nat Genet1999,23,1:1
8Cardiac conduction defects associate with mutations in SCN5A显示文摘Schott JJ Alshinawi C Kyndt F 0,,1:1
9Cardiac conduction defects associated with mutations in SCN5A显示文摘SCHOTT J C KYNDT F 1999Nat Genet1999,23,1:1
10Serial measurement of antineutrophil cytoplasmic autoantibodies in patients with systemic vasculitis显示文摘KYNDT REUMAUX D BRIDOUX F 1999Am J Med1999,106,5:1
11Cardiac conduction defects associate with mutations in SCN5A显示文摘Schott JJ Alshinawi C Kyndt F 1999Nat Genet1999,23,1:1
12Novel SCN5A mutation leading either to isolated cardiac conduction defect or Brugada syndrome in a large French family显示文摘Kyndt F Probst V Potet F 2001Circulation2001,104,25:1
13Cardiac conduction defects associated with mutations in SCN5A 显示文摘Schott JJ Alshinawi C Kyndt F 1999Nature Genetics1999,23,:1
14Cardiac conduction defects associates with mutation in SCN5A 显示文摘Schott J J Alshinawi C Kyndt F 1999Nature Gent1999,23,1:1
15The perception of workload and task complexity and its influence on students' approaches to learning: a study in higher education 显示文摘KYNDT E DOCHY F STRUYVEN K CASCALLAR E 2011European Journal of Psychology of Education2011,,3:1
16Cardiac conduction defects associate with mutations in SCN5A显示文摘Schott JJ Alshinawi C kyndt F 1999Nat Genet1999,23,1:1
17Cardiac conduction defects associate with mutations in SCN5A 显示文摘Schott J J Alshinawi C Kyndt F 1999(Letter) Nature Genet1999,23,:1
18Proximal tubular dysfunction in primary Sjogren's syndrome: a clinicopathological study of2 case显示文摘Bridoux F Kyndt X Abou-Ayache R 2004Clin Nephrol2004,61,3:1
19Mapping of X-linked myxomatous valvular dystrophy to chromosome Xq28显示文摘KYNDT F SCHOTT J J TROCHU J N 1998Am J Hum Genet1998,62,:1
20Cardiac conduction defects associate with mutations in SCN5A显示文摘Schott JJ Alshinawi C Kyndt F 0,,:1
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