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41篇 您的检索式：作者名="Bowles KR"

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	题名	作者	年代	出处	被引量
1	Novel gene mutations in patients with left ventricular noncompaction or barth syndrome显示文摘	Ichida F Tsubata S Bowles KR	2001	Circulation2001，103，9：	1
2	The 'final common pathway' hypothesis and inherited cardiovascular disease:the role of cytoskeletal proteins in dilated cardiomyopathy显示文摘	Bowles NE Bowles KR Towbin JA	2002	Herz2002，25，：	1
3	Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy显示文摘	Tsubata S Bowles KR Vatta M		0，，：	1
4	Mutations in the human dehasarcoglycan gene in familial and sporadic dilated cardiomyopathy 显示文摘	Tsubata S Bowles KR VattaM	2000	J Clin Invest2000，106，：	1
5	Novel gene mutations in pa- tients with left ventricular noncompaction or Barth syndrome 显示文摘	Ichida F Tsubata S Bowles KR	2001	Circulation2001，103，9：	1
6	The 'final common pathway' hypothesis and inherited cardiovascular disease:the role of cytoskeletal proteins in dilated cardiomypathy显示文摘	Bowles NE Bowles KR Towbin JA		0，，：	1
7	显示文摘	Bowles NE Bowles KR Towbin JA	2000	Herz2000，25，：	1
8	Novel gene mutations in patiets with left ventricular noncompaction or Barth Syndrome 显示文摘	chida F Tsubata S Bowles KR	2001	Circulation2001，103，12：	1
9	Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23显示文摘	Bowles KR Gajarski R Porter P	1996	J Clin Invest1996，98，6：	1
10	Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome显示文摘	Ichida F Tsubata S Bowles KR	2001	Circulation2001，103，：	1
11	Novel gene mutations in patients with left ventricular noncompaetion or Barth syndrome显示文摘	Ichida F Tsubata S Bowles KR	2001	Circulation2001，103，9：	1
12	Mutations in the human δ-Sarcoglycan gene in familial and sporadic dilated cardiomyopathy显示文摘	Tsubata S Bowles KR Vatta M	2000	J Clin Invest2000，106，：	1
13	Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy显示文摘	Tsubata S Bowles KR Vatta M	2000	J Clin Invest2000，106，：	1
14	Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome显示文摘	Ichida F Tsubata S Bowles KR	2001	Circulation2001，103，：	1
15	Mutations in the human sarcoglycan gene in familial and sporadic dilated cardiomyopathy显示文摘	Tsubata S Bowles KR Vatta M	2000	J Clin Invest September2000，1065，：	1
16	Novel gene mutations in pa- tients with left ventricular noncompaction or Barth syndrome 显示文摘	Ichida F Tsubata S Bowles KR	2001	Circulation2001，103，9：	1
17	Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome显示文摘	Ichida F Tsubata S Bowles KR	2001	Circulation2001，103，：	1
18	Gene mapping of familial autosomal dominant dilated cardiomyopathy to chromosome 10q21-23 显示文摘	Bowles KR Gajarski R Porter P	1996	J Clin Invest1996，98，：	1
19	The 'final common pathway' hypothesis and inherited cardiovascular disease:the role of cytoskeletal proteins in dilated cardiomyopathy 显示文摘	Bowles NE Bowles KR Towbin JA	2002	Herz2002，25，：	1
20	Gene mapping of familiar autosomal dominant dilated cardiomyopathy to chromosome 10q21-23显示文摘	Gajarski R Porter P	1996	J Clin Invest1996，98，16：	1

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