-
1
-
-
84931292033
-
Long read nanopore sequencing for detection of HLA and CYP2D6 variants and haplotypes
-
Ammar R, Paton TA, Torti D, Shlien A, Bader GD. 2015. Long read nanopore sequencing for detection of HLA and CYP2D6 variants and haplotypes. F1000Res 4:17.
-
(2015)
F1000Res
, vol.4
, pp. 17
-
-
Ammar, R.1
Paton, T.A.2
Torti, D.3
Shlien, A.4
Bader, G.D.5
-
2
-
-
84924388692
-
MinION nanopore sequencing identifies the position and structure of a bacterial antibiotic resistance island
-
Ashton PM, Nair S, Dallman T, Rubino S, Rabsch W, Mwaigwisya S, Wain J, O'Grady J. 2015. MinION nanopore sequencing identifies the position and structure of a bacterial antibiotic resistance island. Nat Biotechnol 33:296-300.
-
(2015)
Nat Biotechnol
, vol.33
, pp. 296-300
-
-
Ashton, P.M.1
Nair, S.2
Dallman, T.3
Rubino, S.4
Rabsch, W.5
Mwaigwisya, S.6
Wain, J.7
O'Grady, J.8
-
3
-
-
84874312025
-
NGSUtils: a software suite for analyzing and manipulating next-generation sequencing datasets
-
Breese MR, Liu Y. 2013. NGSUtils: a software suite for analyzing and manipulating next-generation sequencing datasets. Bioinformatics 29:494-496.
-
(2013)
Bioinformatics
, vol.29
, pp. 494-496
-
-
Breese, M.R.1
Liu, Y.2
-
4
-
-
84866266717
-
Mapping single molecule sequencing reads using basic local alignment with successive refinement (BLASR): application and theory
-
Chaisson MJ, Tesler G. 2012. Mapping single molecule sequencing reads using basic local alignment with successive refinement (BLASR): application and theory. BMC Bioinformatics 13:238.
-
(2012)
BMC Bioinformatics
, vol.13
, pp. 238
-
-
Chaisson, M.J.1
Tesler, G.2
-
5
-
-
84855968708
-
Clinical Pharmacogenetics Implementation Consortium (CPIC) guidelines for codeine therapy in the context of cytochrome P450 2D6 (CYP2D6) genotype
-
Crews KR, Gaedigk A, Dunnenberger HM, Klein TE, Shen DD, Callaghan JT, Kharasch ED, Skaar TC, Clinical Pharmacogenetics Implementation C. 2012. Clinical Pharmacogenetics Implementation Consortium (CPIC) guidelines for codeine therapy in the context of cytochrome P450 2D6 (CYP2D6) genotype. Clin Pharmacol Ther 91:321-326.
-
(2012)
Clin Pharmacol Ther
, vol.91
, pp. 321-326
-
-
Crews, K.R.1
Gaedigk, A.2
Dunnenberger, H.M.3
Klein, T.E.4
Shen, D.D.5
Callaghan, J.T.6
Kharasch, E.D.7
Skaar, T.C.8
-
6
-
-
84897022750
-
Clinical Pharmacogenetics Implementation Consortium guidelines for cytochrome P450 2D6 genotype and codeine therapy: 2014 update
-
Crews KR, Gaedigk A, Dunnenberger HM, Leeder JS, Klein TE, Caudle KE, Haidar CE, Shen DD, Callaghan JT, Sadhasivam S, Prows CA, Kharasch ED, et al. 2014. Clinical Pharmacogenetics Implementation Consortium guidelines for cytochrome P450 2D6 genotype and codeine therapy: 2014 update. Clin Pharmacol Ther 95:376-382.
-
(2014)
Clin Pharmacol Ther
, vol.95
, pp. 376-382
-
-
Crews, K.R.1
Gaedigk, A.2
Dunnenberger, H.M.3
Leeder, J.S.4
Klein, T.E.5
Caudle, K.E.6
Haidar, C.E.7
Shen, D.D.8
Callaghan, J.T.9
Sadhasivam, S.10
Prows, C.A.11
Kharasch, E.D.12
-
7
-
-
79955483667
-
A framework for variation discovery and genotyping using next-generation DNA sequencing data
-
DePristo MA, Banks E, Poplin R, Garimella KV, Maguire JR, Hartl C, Philippakis AA, del Angel G, Rivas MA, Hanna M, McKenna A, Fennell TJ, et al. 2011. A framework for variation discovery and genotyping using next-generation DNA sequencing data. Nat Genet 43:491-498.
-
(2011)
Nat Genet
, vol.43
, 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
-
8
-
-
84927178203
-
Establishment of CYP2D6 reference samples by multiple validated genotyping platforms
-
Fang H, Liu X, Ramirez J, Choudhury N, Kubo M, Im HK, Konkashbaev A, Cox NJ, Ratain MJ, Nakamura Y, O'Donnell PH. 2014. Establishment of CYP2D6 reference samples by multiple validated genotyping platforms. Pharmacogenomics J 14:564-572.
-
(2014)
Pharmacogenomics J
, vol.14
, pp. 564-572
-
-
Fang, H.1
Liu, X.2
Ramirez, J.3
Choudhury, N.4
Kubo, M.5
Im, H.K.6
Konkashbaev, A.7
Cox, N.J.8
Ratain, M.J.9
Nakamura, Y.10
O'Donnell, P.H.11
-
9
-
-
84886690638
-
Complexities of CYP2D6 gene analysis and interpretation
-
Gaedigk A. 2013. Complexities of CYP2D6 gene analysis and interpretation. Int Rev Psychiatry 25:534-553.
-
(2013)
Int Rev Psychiatry
, vol.25
, pp. 534-553
-
-
Gaedigk, A.1
-
10
-
-
33645109079
-
CYP2D6*36 gene arrangements within the cyp2d6 locus: association of CYP2D6*36 with poor metabolizer status
-
Gaedigk A, Bradford LD, Alander SW, Leeder JS. 2006. CYP2D6*36 gene arrangements within the cyp2d6 locus: association of CYP2D6*36 with poor metabolizer status. Drug Metab Dispos 34:563-569.
-
(2006)
Drug Metab Dispos
, vol.34
, pp. 563-569
-
-
Gaedigk, A.1
Bradford, L.D.2
Alander, S.W.3
Leeder, J.S.4
-
11
-
-
33846643134
-
Cytochrome P4502D6 (CYP2D6) gene locus heterogeneity: characterization of gene duplication events
-
Gaedigk A, Ndjountche L, Divakaran K, Dianne Bradford L, Zineh I, Oberlander TF, Brousseau DC, McCarver DG, Johnson JA, Alander SW, Wayne Riggs K, Steven Leeder J. 2007. Cytochrome P4502D6 (CYP2D6) gene locus heterogeneity: characterization of gene duplication events. Clin Pharmacol Ther 81:242-251.
-
(2007)
Clin Pharmacol Ther
, vol.81
, pp. 242-251
-
-
Gaedigk, A.1
Ndjountche, L.2
Divakaran, K.3
Dianne Bradford, L.4
Zineh, I.5
Oberlander, T.F.6
Brousseau, D.C.7
McCarver, D.G.8
Johnson, J.A.9
Alander, S.W.10
Wayne Riggs, K.11
Steven Leeder, J.12
-
12
-
-
84943611363
-
CYP2D6 Haplotype determination using long range allele-specific amplification: resolution of a complex genotype and a discordant genotype involving the CYP2D6*59 allele
-
Gaedigk A, Riffel AK, Leeder JS. 2015. CYP2D6 Haplotype determination using long range allele-specific amplification: resolution of a complex genotype and a discordant genotype involving the CYP2D6*59 allele. J Mol Diagn 17:740-748.
-
(2015)
J Mol Diagn
, vol.17
, pp. 740-748
-
-
Gaedigk, A.1
Riffel, A.K.2
Leeder, J.S.3
-
13
-
-
38349132802
-
The CYP2D6 activity score: translating genotype information into a qualitative measure of phenotype
-
Gaedigk A, Simon SD, Pearce RE, Bradford LD, Kennedy MJ, Leeder JS. 2008. The CYP2D6 activity score: translating genotype information into a qualitative measure of phenotype. Clin Pharmacol Ther 83:234-242.
-
(2008)
Clin Pharmacol Ther
, vol.83
, pp. 234-242
-
-
Gaedigk, A.1
Simon, S.D.2
Pearce, R.E.3
Bradford, L.D.4
Kennedy, M.J.5
Leeder, J.S.6
-
14
-
-
0023854270
-
Characterization of the common genetic defect in humans deficient in debrisoquine metabolism
-
Gonzalez FJ, Skoda RC, Kimura S, Umeno M, Zanger UM, Nebert DW, Gelboin HV, Hardwick JP, Meyer UA. 1988. Characterization of the common genetic defect in humans deficient in debrisoquine metabolism. Nature 331:442-446.
-
(1988)
Nature
, vol.331
, pp. 442-446
-
-
Gonzalez, F.J.1
Skoda, R.C.2
Kimura, S.3
Umeno, M.4
Zanger, U.M.5
Nebert, D.W.6
Gelboin, H.V.7
Hardwick, J.P.8
Meyer, U.A.9
-
15
-
-
0025114258
-
Identification of the primary gene defect at the cytochrome P450 CYP2D locus
-
Gough AC, Miles JS, Spurr NK, Moss JE, Gaedigk A, Eichelbaum M, Wolf CR. 1990. Identification of the primary gene defect at the cytochrome P450 CYP2D locus. Nature 347:773-776.
-
(1990)
Nature
, vol.347
, pp. 773-776
-
-
Gough, A.C.1
Miles, J.S.2
Spurr, N.K.3
Moss, J.E.4
Gaedigk, A.5
Eichelbaum, M.6
Wolf, C.R.7
-
16
-
-
0025080352
-
Genotyping of poor metabolisers of debrisoquine by allele-specific PCR amplification
-
Heim M, Meyer UA. 1990. Genotyping of poor metabolisers of debrisoquine by allele-specific PCR amplification. Lancet 336:529-532.
-
(1990)
Lancet
, vol.336
, pp. 529-532
-
-
Heim, M.1
Meyer, U.A.2
-
17
-
-
84946494342
-
In vivo assessment of the metabolic activity of CYP2D6 diplotypes and alleles
-
Hertz DL, Snavely AC, McLeod HL, Walko CM, Ibrahim JG, Anderson S, Weck KE, Magrinat G, Olajide O, Moore S, Raab R, Carrizosa DR, et al. 2015. In vivo assessment of the metabolic activity of CYP2D6 diplotypes and alleles. Br J Clin Pharmacol 80:1122-1130.
-
(2015)
Br J Clin Pharmacol
, vol.80
, pp. 1122-1130
-
-
Hertz, D.L.1
Snavely, A.C.2
McLeod, H.L.3
Walko, C.M.4
Ibrahim, J.G.5
Anderson, S.6
Weck, K.E.7
Magrinat, G.8
Olajide, O.9
Moore, S.10
Raab, R.11
Carrizosa, D.R.12
-
18
-
-
84962294272
-
Clinical Pharmacogenetics Implementation Consortium (CPIC) guideline for CYP2D6 and CYP2C19 genotypes and dosing of selective serotonin reuptake inhibitors
-
Hicks JK, Bishop JR, Sangkuhl K, Muller DJ, Ji Y, Leckband SG, Leeder JS, Graham RL, Chiulli DL, A LL, Skaar TC, Scott SA, et al. 2015. Clinical Pharmacogenetics Implementation Consortium (CPIC) guideline for CYP2D6 and CYP2C19 genotypes and dosing of selective serotonin reuptake inhibitors. Clin Pharmacol Ther 98:127-134.
-
(2015)
Clin Pharmacol Ther
, vol.98
, pp. 127-134
-
-
Hicks, J.K.1
Bishop, J.R.2
Sangkuhl, K.3
Muller, D.J.4
Ji, Y.5
Leckband, S.G.6
Leeder, J.S.7
Graham, R.L.8
Chiulli, D.L.9
Skaar, T.C.10
Scott, S.A.11
-
19
-
-
84896355622
-
Challenges in CYP2D6 phenotype assignment from genotype data: a critical assessment and call for standardization
-
Hicks JK, Swen JJ, Gaedigk A. 2014. Challenges in CYP2D6 phenotype assignment from genotype data: a critical assessment and call for standardization. Curr Drug Metab 15:218-232.
-
(2014)
Curr Drug Metab
, vol.15
, pp. 218-232
-
-
Hicks, J.K.1
Swen, J.J.2
Gaedigk, A.3
-
20
-
-
84876665512
-
Clinical Pharmacogenetics Implementation Consortium guideline for CYP2D6 and CYP2C19 genotypes and dosing of tricyclic antidepressants
-
Hicks JK, Swen JJ, Thorn CF, Sangkuhl K, Kharasch ED, Ellingrod VL, Skaar TC, Muller DJ, Gaedigk A, Stingl JC, Clinical Pharmacogenetics Implementation C. 2013. Clinical Pharmacogenetics Implementation Consortium guideline for CYP2D6 and CYP2C19 genotypes and dosing of tricyclic antidepressants. Clin Pharmacol Ther 93:402-408.
-
(2013)
Clin Pharmacol Ther
, vol.93
, pp. 402-408
-
-
Hicks, J.K.1
Swen, J.J.2
Thorn, C.F.3
Sangkuhl, K.4
Kharasch, E.D.5
Ellingrod, V.L.6
Skaar, T.C.7
Muller, D.J.8
Gaedigk, A.9
Stingl, J.C.10
-
21
-
-
77951051005
-
Protocol: a simple gel-free method for SNP genotyping using allele-specific primers in rice and other plant species
-
Hirotsu N, Murakami N, Kashiwagi T, Ujiie K, Ishimaru K. 2010. Protocol: a simple gel-free method for SNP genotyping using allele-specific primers in rice and other plant species. Plant Methods 6:12.
-
(2010)
Plant Methods
, vol.6
, pp. 12
-
-
Hirotsu, N.1
Murakami, N.2
Kashiwagi, T.3
Ujiie, K.4
Ishimaru, K.5
-
22
-
-
0024796958
-
The human debrisoquine 4-hydroxylase (CYP2D) locus: sequence and identification of the polymorphic CYP2D6 gene, a related gene, and a pseudogene
-
Kimura S, Umeno M, Skoda RC, Meyer UA, Gonzalez FJ. 1989. The human debrisoquine 4-hydroxylase (CYP2D) locus: sequence and identification of the polymorphic CYP2D6 gene, a related gene, and a pseudogene. Am J Hum Genet 45:889-904.
-
(1989)
Am J Hum Genet
, vol.45
, pp. 889-904
-
-
Kimura, S.1
Umeno, M.2
Skoda, R.C.3
Meyer, U.A.4
Gonzalez, F.J.5
-
23
-
-
84880889177
-
Important and critical scientific aspects in pharmacogenomics analysis: lessons from controversial results of tamoxifen and CYP2D6 studies
-
Kiyotani K, Mushiroda T, Zembutsu H, Nakamura Y. 2013. Important and critical scientific aspects in pharmacogenomics analysis: lessons from controversial results of tamoxifen and CYP2D6 studies. J Hum Genet 58:327-333.
-
(2013)
J Hum Genet
, vol.58
, pp. 327-333
-
-
Kiyotani, K.1
Mushiroda, T.2
Zembutsu, H.3
Nakamura, Y.4
-
24
-
-
84925373900
-
Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM
-
1303.3997v2
-
Li H. 2013. Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM. arXiv 1303.3997v2:1-3.
-
(2013)
arXiv
, pp. 1-3
-
-
Li, H.1
-
25
-
-
84865280408
-
An improved allele-specific PCR primer design method for SNP marker analysis and its application
-
Liu J, Huang S, Sun M, Liu S, Liu Y, Wang W, Zhang X, Wang H, Hua W. 2012. An improved allele-specific PCR primer design method for SNP marker analysis and its application. Plant Methods 8:34.
-
(2012)
Plant Methods
, vol.8
, pp. 34
-
-
Liu, J.1
Huang, S.2
Sun, M.3
Liu, S.4
Liu, Y.5
Wang, W.6
Zhang, X.7
Wang, H.8
Hua, W.9
-
26
-
-
0017695082
-
Polymorphic hydroxylation of Debrisoquine in man
-
Mahgoub A, Idle JR, Dring LG, Lancaster R, Smith RL. 1977. Polymorphic hydroxylation of Debrisoquine in man. Lancet 2:584-586.
-
(1977)
Lancet
, vol.2
, pp. 584-586
-
-
Mahgoub, A.1
Idle, J.R.2
Dring, L.G.3
Lancaster, R.4
Smith, R.L.5
-
27
-
-
84888127394
-
Multi-ethnic cytochrome-P450 copy number profiling: novel pharmacogenetic alleles and mechanism of copy number variation formation
-
Martis S, Mei H, Vijzelaar R, Edelmann L, Desnick RJ, Scott SA. 2013a. Multi-ethnic cytochrome-P450 copy number profiling: novel pharmacogenetic alleles and mechanism of copy number variation formation. Pharmacogenomics J 13:558-566.
-
(2013)
Pharmacogenomics J
, vol.13
, pp. 558-566
-
-
Martis, S.1
Mei, H.2
Vijzelaar, R.3
Edelmann, L.4
Desnick, R.J.5
Scott, S.A.6
-
28
-
-
84881126177
-
Multi-ethnic distribution of clinically relevant CYP2C genotypes and haplotypes
-
Martis S, Peter I, Hulot JS, Kornreich R, Desnick RJ, Scott SA. 2013b. Multi-ethnic distribution of clinically relevant CYP2C genotypes and haplotypes. Pharmacogenomics J 13:369-377.
-
(2013)
Pharmacogenomics J
, vol.13
, pp. 369-377
-
-
Martis, S.1
Peter, I.2
Hulot, J.S.3
Kornreich, R.4
Desnick, R.J.5
Scott, S.A.6
-
29
-
-
77956295988
-
The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data
-
McKenna A, Hanna M, Banks E, Sivachenko A, Cibulskis K, Kernytsky A, Garimella K, Altshuler D, Gabriel S, Daly M, DePristo MA. 2010. The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res 20:1297-1303.
-
(2010)
Genome Res
, vol.20
, 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
-
30
-
-
0020635141
-
Hepatic monooxygenase activities in subjects with a genetic defect in drug oxidation
-
Meier PJ, Mueller HK, Dick B, Meyer UA. 1983. Hepatic monooxygenase activities in subjects with a genetic defect in drug oxidation. Gastroenterology 85:682-692.
-
(1983)
Gastroenterology
, vol.85
, pp. 682-692
-
-
Meier, P.J.1
Mueller, H.K.2
Dick, B.3
Meyer, U.A.4
-
32
-
-
78049396695
-
Characterization of 107 genomic DNA reference materials for CYP2D6, CYP2C19, CYP2C9, VKORC1, and UGT1A1: a GeT-RM and Association for Molecular Pathology collaborative project
-
Pratt VM, Zehnbauer B, Wilson JA, Baak R, Babic N, Bettinotti M, Buller A, Butz K, Campbell M, Civalier C, El-Badry A, Farkas DH, et al. 2010. Characterization of 107 genomic DNA reference materials for CYP2D6, CYP2C19, CYP2C9, VKORC1, and UGT1A1: a GeT-RM and Association for Molecular Pathology collaborative project. J Mol Diagn 12:835-846.
-
(2010)
J Mol Diagn
, vol.12
, pp. 835-846
-
-
Pratt, V.M.1
Zehnbauer, B.2
Wilson, J.A.3
Baak, R.4
Babic, N.5
Bettinotti, M.6
Buller, A.7
Butz, K.8
Campbell, M.9
Civalier, C.10
El-Badry, A.11
Farkas, D.H.12
-
33
-
-
84893732936
-
CYP2D6 genotype and adjuvant tamoxifen: meta-analysis of heterogeneous study populations
-
Province MA, Goetz MP, Brauch H, Flockhart DA, Hebert JM, Whaley R, Suman VJ, Schroth W, Winter S, Zembutsu H, Mushiroda T, Newman WG, et al. 2014. CYP2D6 genotype and adjuvant tamoxifen: meta-analysis of heterogeneous study populations. Clin Pharmacol Ther 95:216-227.
-
(2014)
Clin Pharmacol Ther
, vol.95
, pp. 216-227
-
-
Province, M.A.1
Goetz, M.P.2
Brauch, H.3
Flockhart, D.A.4
Hebert, J.M.5
Whaley, R.6
Suman, V.J.7
Schroth, W.8
Winter, S.9
Zembutsu, H.10
Mushiroda, T.11
Newman, W.G.12
-
34
-
-
79953249419
-
Gene copy number variations: it is important to determine which allele is affected
-
Ramamoorthy A, Skaar TC. 2011. Gene copy number variations: it is important to determine which allele is affected. Pharmacogenomics 12:299-301.
-
(2011)
Pharmacogenomics
, vol.12
, pp. 299-301
-
-
Ramamoorthy, A.1
Skaar, T.C.2
-
35
-
-
80052150179
-
Origins of the E. coli strain causing an outbreak of hemolytic-uremic syndrome in Germany
-
Rasko DA, Webster DR, Sahl JW, Bashir A, Boisen N, Scheutz F, Paxinos EE, Sebra R, Chin CS, Iliopoulos D, Klammer A, Peluso P, et al. 2011. Origins of the E. coli strain causing an outbreak of hemolytic-uremic syndrome in Germany. N Engl J Med 365:709-717.
-
(2011)
N Engl J Med
, vol.365
, pp. 709-717
-
-
Rasko, D.A.1
Webster, D.R.2
Sahl, J.W.3
Bashir, A.4
Boisen, N.5
Scheutz, F.6
Paxinos, E.E.7
Sebra, R.8
Chin, C.S.9
Iliopoulos, D.10
Klammer, A.11
Peluso, P.12
-
36
-
-
79951809825
-
CPIC: Clinical Pharmacogenetics Implementation Consortium of the Pharmacogenomics Research Network
-
Relling MV, Klein TE. 2011. CPIC: Clinical Pharmacogenetics Implementation Consortium of the Pharmacogenomics Research Network. Clin Pharmacol Ther 89:464-467.
-
(2011)
Clin Pharmacol Ther
, vol.89
, pp. 464-467
-
-
Relling, M.V.1
Klein, T.E.2
-
37
-
-
85027954420
-
The Human Cytochrome P450 (CYP) Allele Nomenclature website: a peer-reviewed database of CYP variants and their associated effects
-
Sim SC, Ingelman-Sundberg M. 2010. The Human Cytochrome P450 (CYP) Allele Nomenclature website: a peer-reviewed database of CYP variants and their associated effects. Hum Genomics 4:278-281.
-
(2010)
Hum Genomics
, vol.4
, pp. 278-281
-
-
Sim, S.C.1
Ingelman-Sundberg, M.2
-
38
-
-
0034743396
-
Characterization of the CYP2D6*29 allele commonly present in a black Tanzanian population causing reduced catalytic activity
-
Wennerholm A, Johansson I, Hidestrand M, Bertilsson L, Gustafsson LL, Ingelman-Sundberg M. 2001. Characterization of the CYP2D6*29 allele commonly present in a black Tanzanian population causing reduced catalytic activity. Pharmacogenetics 11:417-427.
-
(2001)
Pharmacogenetics
, vol.11
, pp. 417-427
-
-
Wennerholm, A.1
Johansson, I.2
Hidestrand, M.3
Bertilsson, L.4
Gustafsson, L.L.5
Ingelman-Sundberg, M.6
-
39
-
-
84928812813
-
Quantitative and multiplexed DNA methylation analysis using long-read single-molecule real-time bisulfite sequencing (SMRT-BS)
-
Yang Y, Sebra R, Pullman BS, Qiao W, Peter I, Desnick RJ, Geyer CR, DeCoteau JF, Scott SA. 2015. Quantitative and multiplexed DNA methylation analysis using long-read single-molecule real-time bisulfite sequencing (SMRT-BS). BMC Genomics 16:350.
-
(2015)
BMC Genomics
, vol.16
, pp. 350
-
-
Yang, Y.1
Sebra, R.2
Pullman, B.S.3
Qiao, W.4
Peter, I.5
Desnick, R.J.6
Geyer, C.R.7
DeCoteau, J.F.8
Scott, S.A.9
|