-
1
-
-
17044446589
-
Effectiveness and limitations of β-blocker therapy in congenital long- QT syndrome
-
Moss, A. J; Zareba, W; Hall, W. J; Schwartz, P. J; Crampton, R. S; Benhorin, J; Vincent, G. M; Locati, E. H; Priori, S. G; Napolitano, C; Medina, A; Zhang, L; Robinson, J. L; Timothy, K; Towbin, J. A; & Andrews, M. L. (2000). Effectiveness and limitations of beta-blocker therapy in congenital long-QT syndrome. Circulation, 101(6), 616-623. (Pubitemid 30094732)
-
(2000)
Circulation
, vol.101
, Issue.6
, pp. 616-623
-
-
Moss, A.J.1
Zareba, W.2
Hall, W.J.3
Schwartz, P.J.4
Crampton, R.S.5
Benhorin, J.6
Vincent, G.M.7
Locati, E.H.8
Priori, S.G.9
Napolitano, C.10
Medina, A.11
Zhang, L.12
Robinson, J.L.13
Timothy, K.14
Towbin, J.A.15
Andrews, M.L.16
-
2
-
-
58049135095
-
All LQT3 patients need an ICD: True or false?
-
10.1016/j.hrthm.2008.10.017 19121811 10.1016/j.hrthm.2008.10.017
-
Schwartz, P. J; Spazzolini, C; & Crotti, L. (2009). All LQT3 patients need an ICD: true or false? Heart Rhythm, 6(1), 113-120. doi: 10.1016/j.hrthm.2008.10.017.
-
(2009)
Heart Rhythm
, vol.6
, Issue.1
, pp. 113-120
-
-
Schwartz, P.J.1
Spazzolini, C.2
Crotti, L.3
-
3
-
-
59849102447
-
High efficacy of beta-blockers in long-QT syndrome type 1: Contribution of noncompliance and QT-prolonging drugs to the occurrence of beta-blocker treatment "failures
-
10.1161/circulationaha.108.772533 19118258 10.1161/CIRCULATIONAHA.108. 772533 1:CAS:528:DC%2BD1MXivFeqtw%3D%3D
-
Vincent, G. M; Schwartz, P. J; Denjoy, I; Swan, H; Bithell, C; Spazzolini, C; Crotti, L; Piippo, K; Lupoglazoff, J. M; Villain, E; Priori, S. G; Napolitano, C; & Zhang, L. (2009). High efficacy of beta-blockers in long-QT syndrome type 1: contribution of noncompliance and QT-prolonging drugs to the occurrence of beta-blocker treatment "failures". Circulation, 119(2), 215-221. doi: 10.1161/circulationaha.108.772533.
-
(2009)
Circulation
, vol.119
, Issue.2
, pp. 215-221
-
-
Vincent, G.M.1
Schwartz, P.J.2
Denjoy, I.3
Swan, H.4
Bithell, C.5
Spazzolini, C.6
Crotti, L.7
Piippo, K.8
Lupoglazoff, J.M.9
Villain, E.10
Priori, S.G.11
Napolitano, C.12
Zhang, L.13
-
4
-
-
77955258960
-
Beta-blocker efficacy in high-risk patients with the congenital long-QT syndrome types 1 and 2: Implications for patient management
-
10.1111/j.1540-8167.2010.01737.x 20233272
-
Goldenberg, I; Bradley, J; Moss, A; McNitt, S; Polonsky, S; Robinson, J. L; Andrews, M; & Zareba, W. (2010). Beta-blocker efficacy in high-risk patients with the congenital long-QT syndrome types 1 and 2: implications for patient management. Journal of Cardiovascular Electrophysiology, 21(8), 893-901. doi: 10.1111/j.1540-8167.2010.01737.x.
-
(2010)
Journal of Cardiovascular Electrophysiology
, vol.21
, Issue.8
, pp. 893-901
-
-
Goldenberg, I.1
Bradley, J.2
Moss, A.3
McNitt, S.4
Polonsky, S.5
Robinson, J.L.6
Andrews, M.7
Zareba, W.8
-
5
-
-
73149125834
-
Mutation-specific risk in two genetic forms of type 3 long QT syndrome
-
10.1016/j.amjcard.2009.08.676 20102920 10.1016/j.amjcard.2009.08.676 1:CAS:528:DC%2BC3cXosVah
-
Liu, J. F; Moss, A. J; Jons, C; Benhorin, J; Schwartz, P. J; Spazzolini, C; Crotti, L; Ackerman, M. J; McNitt, S; Robinson, J. L; Qi, M; Goldenberg, I; & Zareba, W. (2010). Mutation-specific risk in two genetic forms of type 3 long QT syndrome. The American Journal of Cardiology, 105(2), 210-213. doi: 10.1016/j.amjcard.2009.08.676.
-
(2010)
The American Journal of Cardiology
, vol.105
, Issue.2
, pp. 210-213
-
-
Liu, J.F.1
Moss, A.J.2
Jons, C.3
Benhorin, J.4
Schwartz, P.J.5
Spazzolini, C.6
Crotti, L.7
Ackerman, M.J.8
McNitt, S.9
Robinson, J.L.10
Qi, M.11
Goldenberg, I.12
Zareba, W.13
-
6
-
-
80051710052
-
HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: This document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)
-
10.1093/europace/eur245 21810866 10.1093/europace/eur245
-
Ackerman, M. J; Priori, S. G; Willems, S; Berul, C; Brugada, R; Calkins, H; Camm, A. J; Ellinor, P. T; Gollob, M; Hamilton, R; Hershberger, R. E; Judge, D. P; Le Marec, H; McKenna, W. J; Schulze-Bahr, E; Semsarian, C; Towbin, J. A; Watkins, H; Wilde, A; Wolpert, C; & Zipes, D. P. (2011). HRS/EHRA expert consensus statement on the state of genetic testing for the channelopathies and cardiomyopathies: this document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA). Europace, 13(8), 1077-1109. doi: 10.1093/europace/eur245.
-
(2011)
Europace
, vol.13
, Issue.8
, pp. 1077-1109
-
-
Ackerman, M.J.1
Priori, S.G.2
Willems, S.3
Berul, C.4
Brugada, R.5
Calkins, H.6
Camm, A.J.7
Ellinor, P.T.8
Gollob, M.9
Hamilton, R.10
Hershberger, R.E.11
Judge, D.P.12
Le Marec, H.13
McKenna, W.J.14
Schulze-Bahr, E.15
Semsarian, C.16
Towbin, J.A.17
Watkins, H.18
Wilde, A.19
Wolpert, C.20
Zipes, D.P.21
more..
-
7
-
-
70449435450
-
The genetic basis of long QT and short QT syndromes: A mutation update
-
10.1002/humu.21106 19862833 10.1002/humu.21106 1:CAS:528: DC%2BD1MXhsVyqsrfM
-
Hedley, P. L; Jorgensen, P; Schlamowitz, S; Wangari, R; Moolman-Smook, J; Brink, P. A; Kanters, J. K; Corfield, V. A; & Christiansen, M. (2009). The genetic basis of long QT and short QT syndromes: a mutation update. Human Mutation, 30(11), 1486-1511. doi: 10.1002/humu.21106.
-
(2009)
Human Mutation
, vol.30
, Issue.11
, pp. 1486-1511
-
-
Hedley, P.L.1
Jorgensen, P.2
Schlamowitz, S.3
Wangari, R.4
Moolman-Smook, J.5
Brink, P.A.6
Kanters, J.K.7
Corfield, V.A.8
Christiansen, M.9
-
8
-
-
0017681196
-
DNA sequencing with chain-terminating inhibitors
-
271968 10.1073/pnas.74.12.5463 1:CAS:528:DyaE1cXhtlaru7Y%3D
-
Sanger, F; Nicklen, S; & Coulson, A. R. (1977). DNA sequencing with chain-terminating inhibitors. Proceedings of the National Academy of Sciences of the United States of America, 74(12), 5463-5467.
-
(1977)
Proceedings of the National Academy of Sciences of the United States of America
, vol.74
, Issue.12
, pp. 5463-5467
-
-
Sanger, F.1
Nicklen, S.2
Coulson, A.R.3
-
9
-
-
72849144434
-
Sequencing technologies - The next generation
-
10.1038/nrg2626 19997069 10.1038/nrg2626 1:CAS:528:DC%2BD1MXhsFOht7fO
-
Metzker, M. L. (2010). Sequencing technologies - the next generation. Nature Reviews Genetics, 11(1), 31-46. doi: 10.1038/nrg2626.
-
(2010)
Nature Reviews Genetics
, vol.11
, Issue.1
, pp. 31-46
-
-
Metzker, M.L.1
-
10
-
-
80053438889
-
Targeted resequencing of the EGFR and MET genes using the Fluidigm Access Array System and the Roche GS Junior System
-
10.2144/000113740 10.2144/000113740
-
Teiling, C; & Pieprzyk, M. (2011). Targeted resequencing of the EGFR and MET genes using the Fluidigm Access Array System and the Roche GS Junior System. Biotechniques, 51(3), 198-199. doi: 10.2144/000113740.
-
(2011)
Biotechniques
, vol.51
, Issue.3
, pp. 198-199
-
-
Teiling, C.1
Pieprzyk, M.2
-
11
-
-
59849113821
-
Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing
-
10.1038/nbt.1523 19182786 10.1038/nbt.1523 1:CAS:528:DC%2BD1MXht1ehs7o%3D
-
Gnirke, A; Melnikov, A; Maguire, J; Rogov, P; LeProust, E. M; Brockman, W; Fennell, T; Giannoukos, G; Fisher, S; Russ, C; Gabriel, S; Jaffe, D. B; Lander, E. S; & Nusbaum, C. (2009). Solution hybrid selection with ultra-long oligonucleotides for massively parallel targeted sequencing. Nature Biotechnology, 27(2), 182-189. doi: 10.1038/nbt.1523.
-
(2009)
Nature Biotechnology
, vol.27
, Issue.2
, pp. 182-189
-
-
Gnirke, A.1
Melnikov, A.2
Maguire, J.3
Rogov, P.4
Leproust, E.M.5
Brockman, W.6
Fennell, T.7
Giannoukos, G.8
Fisher, S.9
Russ, C.10
Gabriel, S.11
Jaffe, D.B.12
Lander, E.S.13
Nusbaum, C.14
-
12
-
-
75349097525
-
Enrichment of sequencing targets from the human genome by solution hybridization
-
10.1186/gb-2009-10-10-r116 19835619 10.1186/gb-2009-10-10-r116
-
Tewhey, R; Nakano, M; Wang, X; Pabon-Pena, C; Novak, B; Giuffre, A; Lin, E; Happe, S; Roberts, D. N; LeProust, E. M; Topol, E. J; Harismendy, O; & Frazer, K. A. (2009). Enrichment of sequencing targets from the human genome by solution hybridization. Genome Biology, 10(10), R116. doi: 10.1186/gb-2009-10- 10-r116.
-
(2009)
Genome Biology
, vol.10
, Issue.10
, pp. 116
-
-
Tewhey, R.1
Nakano, M.2
Wang, X.3
Pabon-Pena, C.4
Novak, B.5
Giuffre, A.6
Lin, E.7
Happe, S.8
Roberts, D.N.9
Leproust, E.M.10
Topol, E.J.11
Harismendy, O.12
Frazer, K.A.13
-
13
-
-
71849090068
-
The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT Syndrome: A comprehensive open reading frame mutational analysis
-
19926015 10.1016/j.jacc.2009.08.022 1:CAS:528:DC%2BC3cXit1ymtw%3D%3D
-
Medeiros-Domingo, A; Bhuiyan, Z. A; Tester, D. J; Hofman, N; Bikker, H; van Tintelen, J. P; Mannens, M. M. A. M; Wilde, A. A. M; & Ackerman, M. J. (2009). The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT Syndrome: a comprehensive open reading frame mutational analysis. Journal of the American College of Cardiology, 54(22), 2065-2074.
-
(2009)
Journal of the American College of Cardiology
, vol.54
, Issue.22
, pp. 2065-2074
-
-
Medeiros-Domingo, A.1
Bhuiyan, Z.A.2
Tester, D.J.3
Hofman, N.4
Bikker, H.5
Van Tintelen, J.P.6
Mannens, M.7
Wilde, A.A.M.8
Ackerman, M.J.9
-
14
-
-
78651289449
-
Ensembl 2011
-
Database Issue 10.1093/nar/gkq1064 21045057 10.1093/nar/gkq1064
-
Flicek, P; Amode, M. R; Barrell, D; Beal, K; Brent, S; Chen, Y; et al. (2011). Ensembl 2011. Nucleic Acids Research, 39(Database issue), D800-D806. doi: 10.1093/nar/gkq1064.
-
(2011)
Nucleic Acids Research
, vol.39
-
-
Flicek, P.1
Amode, M.R.2
Barrell, D.3
Beal, K.4
Brent, S.5
Chen, Y.6
-
15
-
-
79955483667
-
A framework for variation discovery and genotyping using next-generation DNA sequencing data
-
10.1038/ng.806 21478889 10.1038/ng.806 1:CAS:528:DC%2BC3MXksFWguro%3D
-
DePristo, M. A; Banks, E; Poplin, R; Garimella, K. V; Maguire, J. R; Hartl, C; Philippakis, A. A; del Angel, G; Rivas, M. A; Hanna, M; McKenna, A; Fennell, T. J; Kernytsky, A. M; Sivachenko, A. Y; Cibulskis, K; Gabriel, S. B; Altshuler, D; & Daly, M. J. (2011). A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nature Genetics, 43(5), 491-498. doi: 10.1038/ng.806.
-
(2011)
Nature Genetics
, vol.43
, Issue.5
, pp. 491-498
-
-
Depristo, M.A.1
Banks, E.2
Poplin, R.3
Garimella, K.V.4
Maguire, J.R.5
Hartl, C.6
Philippakis, A.A.7
Del Angel, G.8
Rivas, M.A.9
Hanna, M.10
McKenna, A.11
Fennell, T.J.12
Kernytsky, A.M.13
Sivachenko, A.Y.14
Cibulskis, K.15
Gabriel, S.B.16
Altshuler, D.17
Daly, M.J.18
-
16
-
-
67649884743
-
Fast and accurate short read alignment with Burrows-Wheeler transform
-
10.1093/bioinformatics/btp324 19451168 10.1093/bioinformatics/btp324 1:CAS:528:DC%2BD1MXot1Cjtbo%3D
-
Li, H; & Durbin, R. (2009). Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics, 25(14), 1754-1760. doi: 10.1093/bioinformatics/btp324.
-
(2009)
Bioinformatics
, vol.25
, Issue.14
, pp. 1754-1760
-
-
Li, H.1
Durbin, R.2
-
17
-
-
77949587649
-
Fast and accurate long-read alignment with Burrows-Wheeler transform
-
10.1093/bioinformatics/btp698 20080505 10.1093/bioinformatics/btp698
-
Li, H; & Durbin, R. (2010). Fast and accurate long-read alignment with Burrows-Wheeler transform. Bioinformatics, 26(5), 589-595. doi: 10.1093/bioinformatics/btp698.
-
(2010)
Bioinformatics
, vol.26
, Issue.5
, pp. 589-595
-
-
Li, H.1
Durbin, R.2
-
18
-
-
68549104404
-
The Sequence Alignment/Map Format and SAMtools
-
10.1093/bioinformatics/btp352 19505943 10.1093/bioinformatics/btp352
-
Li, H; Handsaker, B; Wysoker, A; Fennell, T; Ruan, J; Homer, N; Marth, G; Abecasis, G; & Durbin, R. (2009). The Sequence Alignment/Map Format and SAMtools. Bioinformatics, 25(16), 2078-2079. doi: 10.1093/bioinformatics/btp352.
-
(2009)
Bioinformatics
, vol.25
, Issue.16
, pp. 2078-2079
-
-
Li, H.1
Handsaker, B.2
Wysoker, A.3
Fennell, T.4
Ruan, J.5
Homer, N.6
Marth, G.7
Abecasis, G.8
Durbin, R.9
-
19
-
-
77951770756
-
BEDTools: A flexible suite of utilities for comparing genomic features
-
10.1093/bioinformatics/btq033 20110278 10.1093/bioinformatics/btq033 1:CAS:528:DC%2BC3cXivFGkurc%3D
-
Quinlan, A. R; & Hall, I. M. (2010). BEDTools: a flexible suite of utilities for comparing genomic features. Bioinformatics, 26(6), 841-842. doi: 10.1093/bioinformatics/btq033.
-
(2010)
Bioinformatics
, vol.26
, Issue.6
, pp. 841-842
-
-
Quinlan, A.R.1
Hall, I.M.2
-
20
-
-
77956295988
-
The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
-
10.1101/gr.107524.110 20644199 10.1101/gr.107524.110 1:CAS:528: DC%2BC3cXhtFeru7jM
-
McKenna, A; Hanna, M; Banks, E; Sivachenko, A; Cibulskis, K; Kernytsky, A; Garimella, K; Altshuler, D; Gabriel, S; Daly, M; & DePristo, M. A. (2010). The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Research, 20(9), 1297-1303. doi: 10.1101/gr.107524.110.
-
(2010)
Genome Research
, vol.20
, Issue.9
, pp. 1297-1303
-
-
McKenna, A.1
Hanna, M.2
Banks, E.3
Sivachenko, A.4
Cibulskis, K.5
Kernytsky, A.6
Garimella, K.7
Altshuler, D.8
Gabriel, S.9
Daly, M.10
Depristo, M.A.11
-
21
-
-
77954091424
-
Accurate SNP and mutation detection by targeted custom microarray-based genomic enrichment of short-fragment sequencing libraries
-
10.1093/nar/gkq072 20164091 10.1093/nar/gkq072
-
Mokry, M; Feitsma, H; Nijman, I. J; de Bruijn, E; van der Zaag, P. J; Guryev, V; & Cuppen, E. (2010). Accurate SNP and mutation detection by targeted custom microarray-based genomic enrichment of short-fragment sequencing libraries. Nucleic Acids Research, 38(10), e116. doi: 10.1093/nar/gkq072.
-
(2010)
Nucleic Acids Research
, vol.38
, Issue.10
, pp. 116
-
-
Mokry, M.1
Feitsma, H.2
Nijman, I.J.3
De Bruijn, E.4
Van Der Zaag, P.J.5
Guryev, V.6
Cuppen, E.7
-
22
-
-
77951967863
-
A database and API for variation, dense genotyping and resequencing data
-
10.1186/1471-2105-11-238 20459810 10.1186/1471-2105-11-238
-
Rios, D; McLaren, W. M; Chen, Y; Birney, E; Stabenau, A; Flicek, P; & Cunningham, F. (2010). A database and API for variation, dense genotyping and resequencing data. BMC Bioinformatics, 11, 238. doi: 10.1186/1471-2105-11-238.
-
(2010)
BMC Bioinformatics
, vol.11
, pp. 238
-
-
Rios, D.1
McLaren, W.M.2
Chen, Y.3
Birney, E.4
Stabenau, A.5
Flicek, P.6
Cunningham, F.7
-
23
-
-
0037903275
-
Human Gene Mutation Database (HGMD®): 2003 Update
-
DOI 10.1002/humu.10212
-
Stenson, P. D; Ball, E. V; Mort, M; Phillips, A. D; Shiel, J. A; Thomas, N. S; Abeysinghe, S; Krawczak, M; & Cooper, D. N. (2003). Human gene mutation database (HGMD): 2003 update. Human Mutation, 21(6), 577-581. doi: 10.1002/humu.10212. (Pubitemid 36667346)
-
(2003)
Human Mutation
, vol.21
, Issue.6
, pp. 577-581
-
-
Stenson, P.D.1
Ball, E.V.2
Mort, M.3
Phillips, A.D.4
Shiel, J.A.5
Thomas, N.S.T.6
Abeysinghe, S.7
Krawczak, M.8
Cooper, D.N.9
-
24
-
-
82555179730
-
Two-sided exact tests and matching confidence intervals for discrete data
-
Fay, M. (2010). Two-sided exact tests and matching confidence intervals for discrete data. R Journal, 2(1), 53-58.
-
(2010)
R Journal
, vol.2
, Issue.1
, pp. 53-58
-
-
Fay, M.1
-
25
-
-
80054757012
-
Performance comparison of exome DNA sequencing technologies
-
10.1038/nbt.1975 21947028 10.1038/nbt.1975 1:CAS:528:DC%2BC3MXht1anu73L
-
Clark, M. J; Chen, R; Lam, H. Y. K; Karczewski, K. J; Chen, R; Euskirchen, G; Butte, A. J; & Snyder, M. (2011). Performance comparison of exome DNA sequencing technologies. Nature Biotechnology, 29(10), 908-914. doi: 10.1038/nbt.1975.
-
(2011)
Nature Biotechnology
, vol.29
, Issue.10
, pp. 908-914
-
-
Clark, M.J.1
Chen, R.2
Lam, H.Y.K.3
Karczewski, K.J.4
Chen, R.5
Euskirchen, G.6
Butte, A.J.7
Snyder, M.8
-
26
-
-
80053446554
-
Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV
-
10.1093/bioinformatics/btr462 21828086 10.1093/bioinformatics/btr462 1:CAS:528:DC%2BC3MXht1eisLzJ
-
Sathirapongsasuti, J. F; Lee, H; Horst, B. A; Brunner, G; Cochran, A. J; Binder, S; Quackenbush, J; & Nelson, S. F. (2011). Exome sequencing-based copy-number variation and loss of heterozygosity detection: ExomeCNV. Bioinformatics, 27(19), 2648-2654. doi: 10.1093/bioinformatics/btr462.
-
(2011)
Bioinformatics
, vol.27
, Issue.19
, pp. 2648-2654
-
-
Sathirapongsasuti, J.F.1
Lee, H.2
Horst, B.A.3
Brunner, G.4
Cochran, A.J.5
Binder, S.6
Quackenbush, J.7
Nelson, S.F.8
-
27
-
-
79957486466
-
Targeted next-generation sequencing for the molecular genetic diagnostics of cardiomyopathies
-
10.1161/circgenetics.110.958322 21252143 10.1161/CIRCGENETICS.110.958322 1:CAS:528:DC%2BC3MXntFClsb4%3D
-
Meder, B; Haas, J; Keller, A; Heid, C; Just, S; Borries, A; Boisguerin, V; Scharfenberger-Schmeer, M; Stahler, P; Beier, M; Weichenhan, D; Strom, T. M; Pfeufer, A; Korn, B; Katus, H. A; & Rottbauer, W. (2011). Targeted next-generation sequencing for the molecular genetic diagnostics of cardiomyopathies. Circulation Cardiovascular Genetics, 4(2), 110-122. doi: 10.1161/circgenetics.110.958322.
-
(2011)
Circulation Cardiovascular Genetics
, vol.4
, Issue.2
, pp. 110-122
-
-
Meder, B.1
Haas, J.2
Keller, A.3
Heid, C.4
Just, S.5
Borries, A.6
Boisguerin, V.7
Scharfenberger-Schmeer, M.8
Stahler, P.9
Beier, M.10
Weichenhan, D.11
Strom, T.M.12
Pfeufer, A.13
Korn, B.14
Katus, H.A.15
Rottbauer, W.16
-
28
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
1000 Genomes Project Consortium 10.1038/nature09534 10.1038/nature09534
-
- 1000 Genomes Project Consortium. (2010). A map of human genome variation from population-scale sequencing. Nature, 467(7319), 1061-1073. doi: 10.1038/nature09534.
-
(2010)
Nature
, vol.467
, Issue.7319
, pp. 1061-1073
-
-
-
29
-
-
27744480028
-
Targeted mutational analysis of ankyrin-B in 541 consecutive, unrelated patients referred for long QT syndrome genetic testing and 200 healthy subjects
-
DOI 10.1016/j.hrthm.2005.07.026, PII S1547527105018916
-
Sherman, J; Tester, D. J; & Ackerman, M. J. (2005). Targeted mutational analysis of ankyrin-B in 541 consecutive, unrelated patients referred for long QT syndrome genetic testing and 200 healthy subjects. Heart Rhythm, 2(11), 1218-1223. doi: 10.1016/j.hrthm.2005.07.026. (Pubitemid 41614167)
-
(2005)
Heart Rhythm
, vol.2
, Issue.11
, pp. 1218-1223
-
-
Sherman, J.1
Tester, D.J.2
Ackerman, M.J.3
-
30
-
-
84872602981
-
Parallel preparation of targeted resequencing libraries from 480 genomic regions using multiplex PCR on the Access Array system [Abstract]
-
Washington, DC. Philadelphia (PA), 2010 Apr 17-21
-
Kaper, F; Wang, J; Anderson, M. J; Chen, P; Lin, M; Pieprzyk, M; et al. (2010) Parallel preparation of targeted resequencing libraries from 480 genomic regions using multiplex PCR on the Access Array system [Abstract]. Paper presented at the Proceedings of the 101st Annual Meeting of the American Association for Cancer Research, Washington, DC. Philadelphia (PA), 2010 Apr 17-21.
-
(2010)
Paper Presented at the Proceedings of the 101st Annual Meeting of the American Association for Cancer Research
-
-
Kaper, F.1
Wang, J.2
Anderson M., .J.3
Chen, P.4
Lin, M.5
Pieprzyk, M.6
|