-
1
-
-
31544452797
-
Clinical patterns and characteristics of uveitis in a tertiary center for uveitis in China
-
Yang P, Zhang Z, Zhou H, Li B, Huang X, Gao Y, Zhu L, Ren Y, Klooster J, Kijlstra A. Clinical patterns and characteristics of uveitis in a tertiary center for uveitis in China. Curr Eye Res 2005; 30:943-8.
-
(2005)
Curr Eye Res
, vol.30
, pp. 943-948
-
-
Yang, P.1
Zhang, Z.2
Zhou, H.3
Li, B.4
Huang, X.5
Gao, Y.6
Zhu, L.7
Ren, Y.8
Klooster, J.9
Kijlstra, A.10
-
4
-
-
33847147967
-
Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients
-
Yang P, Ren Y, Li B, Fang W, Meng Q, Kijlstra A. Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients. Ophthalmology 2007; 114:606-14.
-
(2007)
Ophthalmology
, vol.114
, pp. 606-614
-
-
Yang, P.1
Ren, Y.2
Li, B.3
Fang, W.4
Meng, Q.5
Kijlstra, A.6
-
5
-
-
0028651897
-
Vogt-Koyanagi-Harada disease in identical twins
-
Ishikawa A, Shiono T, Uchida S. Vogt-Koyanagi-Harada disease in identical twins. Retina 1994; 14:435-7.
-
(1994)
Retina
, vol.14
, pp. 435-437
-
-
Ishikawa, A.1
Shiono, T.2
Uchida, S.3
-
7
-
-
0026609914
-
Vogt-Koyanagi-Harada disease in monozygotic twins
-
Itho S, Kurimoto S, Kouno T. Vogt-Koyanagi-Harada disease in monozygotic twins. Int Ophthalmol 1992; 16:49-54.
-
(1992)
Int Ophthalmol
, vol.16
, pp. 49-54
-
-
Itho, S.1
Kurimoto, S.2
Kouno, T.3
-
8
-
-
0026032463
-
Association of HLA antigens with Vogt-Koyanagi-Harada syndrome in a Han Chinese population
-
Zhao M, Jiang Y, Abrahams IW. Association of HLA antigens with Vogt-Koyanagi-Harada syndrome in a Han Chinese population. Arch Ophthalmol 1991: 109:368-70.
-
(1991)
Arch Ophthalmol
, vol.109
, pp. 368-370
-
-
Zhao, M.1
Jiang, Y.2
Abrahams, I.W.3
-
9
-
-
0026693528
-
Profiling human leukocyte antigens in Vogt-Koyanagi-Harada syndrome
-
Zhang XY, Wang XM, Hu TS. Profiling human leukocyte antigens in Vogt-Koyanagi-Harada syndrome. Am J Ophthalmol 1992; 113:567-72.
-
(1992)
Am J Ophthalmol
, vol.113
, pp. 567-572
-
-
Zhang, X.Y.1
Wang, X.M.2
Hu, T.S.3
-
10
-
-
0028044047
-
HLA class II genes in Vogt-Koyanagi-Harada, disease
-
Islam SM, Numaga J, Fujino Y, Hirata R, Matsuki K, Maeda H, Masuda K. HLA class II genes in Vogt-Koyanagi-Harada, disease. Invest Ophthalmol Vis Sci 1994; 35:3890-6.
-
(1994)
Invest Ophthalmol Vis Sci
, vol.35
, pp. 3890-3896
-
-
Islam, S.M.1
Numaga, J.2
Fujino, Y.3
Hirata, R.4
Matsuki, K.5
Maeda, H.6
Masuda, K.7
-
11
-
-
40849101534
-
Association of the CTLA-4 gene with Vogt-Koyanagi-Harada syndrome
-
Du L, Yang P, Hou S, Lin X, Zhou H, Huang X, Wang L, Kijlstra A. Association of the CTLA-4 gene with Vogt-Koyanagi-Harada syndrome. Clin Immunol 2008; 127:43-8.
-
(2008)
Clin Immunol
, vol.127
, pp. 43-48
-
-
Du, L.1
Yang, P.2
Hou, S.3
Lin, X.4
Zhou, H.5
Huang, X.6
Wang, L.7
Kijlstra, A.8
-
12
-
-
33846024381
-
Tyrosinase gene family and Vogt-Koyanagi-Harada disease in Japanese patients
-
Horie Y, Takemoto Y, Miyazaki A, Namba K, Kase S, Yoshida K, Ota M, Hasumi Y, Inoko H, Mizuki N, Ohno S. Tyrosinase gene family and Vogt-Koyanagi-Harada disease in Japanese patients. Mol Vis 2006; 12:1601-5.
-
(2006)
Mol Vis
, vol.12
, pp. 1601-1605
-
-
Horie, Y.1
Takemoto, Y.2
Miyazaki, A.3
Namba, K.4
Kase, S.5
Yoshida, K.6
Ota, M.7
Hasumi, Y.8
Inoko, H.9
Mizuki, N.10
Ohno, S.11
-
13
-
-
37549055779
-
Polymorphism of IFN-gamma gene and Vogt-Koyanagi-Harada disease
-
Horie Y, Kitaichi N, Takemoto Y, Namba K, Yoshida K, Hirose S, Hasumi Y, Ota M, Inoko H, Mizuki N, Ohno S. Polymorphism of IFN-gamma gene and Vogt-Koyanagi-Harada disease. Mol Vis 2007; 13:2334-8.
-
(2007)
Mol Vis
, vol.13
, pp. 2334-2338
-
-
Horie, Y.1
Kitaichi, N.2
Takemoto, Y.3
Namba, K.4
Yoshida, K.5
Hirose, S.6
Hasumi, Y.7
Ota, M.8
Inoko, H.9
Mizuki, N.10
Ohno, S.11
-
14
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
Wellcome Trust Case Control Consortium
-
Wellcome Trust Case Control Consortium. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls. Nature 2007; 447:661-78.
-
(2007)
Nature
, vol.447
, pp. 661-678
-
-
-
15
-
-
33846608131
-
A large-scale genetic association study confirms IL12B and leads to the identification of IL23R psoriasis-risk genes
-
Cargill M, Schrodi SJ, Chang M, Garcia VE, Brandon R, Callis KP, Matsunami N, Ardlie KG, Civello D, Catanese JJ, Leong DU, Panko JM, McAllister LB, Hansen CB, Papenfuss J, Prescott SM, White TJ, Leppert ME, Krueger GG, Begovich AB. A large-scale genetic association study confirms IL12B and leads to the identification of IL23R psoriasis-risk genes. Am J Hum Genet 2007; 80:273-90.
-
(2007)
Am J Hum Genet
, vol.80
, pp. 273-290
-
-
Cargill, M.1
Schrodi, S.J.2
Chang, M.3
Garcia, V.E.4
Brandon, R.5
Callis, K.P.6
Matsunami, N.7
Ardlie, K.G.8
Civello, D.9
Catanese, J.J.10
Leong, D.U.11
Panko, J.M.12
McAllister, L.B.13
Hansen, C.B.14
Papenfuss, J.15
Prescott, S.M.16
White, T.J.17
Leppert, M.E.18
Krueger, G.G.19
Begovich, A.B.20
more..
-
16
-
-
35748981184
-
-
Burton PR, Clayton DG, Cardon LR, Craddock N, Deloukas P, Duncanson A, Kwiatkowski DP, McCarthy MI, Ouwehand WH, Samani NJ, Todd JA, Donnelly P, Barrett JC, Davison D, Easton D, Evans DM, Leung HT, Marchini JL, Morris AP, Spencer CC, Tobin MD, Attwood AP, Boorman JP, Cant B, Everson U, Hussey JM, Jolley JD, Knight AS, Koch K, Meech E, Nutland S, Prowse CV, Stevens HE, Taylor NC, Walters GR, Walker NM, Watkins NA, Winzer T, Jones RW, McArdle WL, Ring SM, Strachan DP, Pembrey M, Breen G, St Clair D, Caesar S, Gordon-Smith K, Jones L, Fraser C, Green EK, Grozeva D, Hamshere ML, Holmans PA, Jones IR, Kirov G, Moskivina. V, Nikolov I, O'Donovan MC, Owen MJ, Collier DA, Elkin A, Farmer A, Williamson R, McGuffin P, Young AH, Ferrier IN, Ball SG, Balmforth AJ, Barrett JH, Bishop TD, Iles MM, Maqbool A, Yuldasheva N, Hall AS, Braund PS, Dixon RJ, Mangino M, Stevens S, Thompson JR, Bredin F, Tremelling M, Parkes M, Drummond H, Lees CW, Nimmo ER, Satsangi J, Fisher SA, Forbes A, Lewis CM, Onnie C
-
Burton PR, Clayton DG, Cardon LR, Craddock N, Deloukas P, Duncanson A, Kwiatkowski DP, McCarthy MI, Ouwehand WH, Samani NJ, Todd JA, Donnelly P, Barrett JC, Davison D, Easton D, Evans DM, Leung HT, Marchini JL, Morris AP, Spencer CC, Tobin MD, Attwood AP, Boorman JP, Cant B, Everson U, Hussey JM, Jolley JD, Knight AS, Koch K, Meech E, Nutland S, Prowse CV, Stevens HE, Taylor NC, Walters GR, Walker NM, Watkins NA, Winzer T, Jones RW, McArdle WL, Ring SM, Strachan DP, Pembrey M, Breen G, St Clair D, Caesar S, Gordon-Smith K, Jones L, Fraser C, Green EK, Grozeva D, Hamshere ML, Holmans PA, Jones IR, Kirov G, Moskivina. V, Nikolov I, O'Donovan MC, Owen MJ, Collier DA, Elkin A, Farmer A, Williamson R, McGuffin P, Young AH, Ferrier IN, Ball SG, Balmforth AJ, Barrett JH, Bishop TD, Iles MM, Maqbool A, Yuldasheva N, Hall AS, Braund PS, Dixon RJ, Mangino M, Stevens S, Thompson JR, Bredin F, Tremelling M, Parkes M, Drummond H, Lees CW, Nimmo ER, Satsangi J, Fisher SA, Forbes A, Lewis CM, Onnie CM, Prescott NJ, Sanderson J, Matthew CG, Barbour J, Mohiuddin MK, Todhunter CE, Mansfield JC, Ahmad T, Cummings FR, Jewell DP, et al. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoinummity variants. Nat Genet 2007; 39:1329-37.
-
-
-
-
17
-
-
33845340501
-
A genome-wide association study identifies IL23R as an inflammatory bowel disease gene
-
Duerr RH, Taylor KD, Brant SR, Rioux JD, Silverberg MS, Daly MJ, Steinhart AH, Abraham C, Regueiro M, Griffiths A, Dassopoulos T, Bitton A, Yang H, Targan S, Datta LW, Kistner EO, Schumm LP, Lee AT, Gregersen PK, Barmada MM, Rotter JI, Nicolae DL, Cho JH. A genome-wide association study identifies IL23R as an inflammatory bowel disease gene. Science 2006; 314:1461-3.
-
(2006)
Science
, vol.314
, pp. 1461-1463
-
-
Duerr, R.H.1
Taylor, K.D.2
Brant, S.R.3
Rioux, J.D.4
Silverberg, M.S.5
Daly, M.J.6
Steinhart, A.H.7
Abraham, C.8
Regueiro, M.9
Griffiths, A.10
Dassopoulos, T.11
Bitton, A.12
Yang, H.13
Targan, S.14
Datta, L.W.15
Kistner, E.O.16
Schumm, L.P.17
Lee, A.T.18
Gregersen, P.K.19
Barmada, M.M.20
Rotter, J.I.21
Nicolae, D.L.22
Cho, J.H.23
more..
-
18
-
-
3543046736
-
A functional variant of SUMO4, a new I kappa B alpha modifier, is associated with type 1 diabetes
-
Guo D, Li M, Zhang Y, Yang P, Eckenrode S, Hopkins D, Zheng W, Purohit S, Podolsky RH, Muir A, Wang J, Dong Z, Brusko T, Atkinson M, Pozzilli P, Zeidler A, Raffel LJ, Jacob CO, Park Y, Serrano-Rios M, Larrad MT, Zhang Z, Garchon HJ, Bach JF, Rotter JI, She JX, Wang CY. A functional variant of SUMO4, a new I kappa B alpha modifier, is associated with type 1 diabetes. Nat Genet 2004; 36:837-41.
-
(2004)
Nat Genet
, vol.36
, pp. 837-841
-
-
Guo, D.1
Li, M.2
Zhang, Y.3
Yang, P.4
Eckenrode, S.5
Hopkins, D.6
Zheng, W.7
Purohit, S.8
Podolsky, R.H.9
Muir, A.10
Wang, J.11
Dong, Z.12
Brusko, T.13
Atkinson, M.14
Pozzilli, P.15
Zeidler, A.16
Raffel, L.J.17
Jacob, C.O.18
Park, Y.19
Serrano-Rios, M.20
Larrad, M.T.21
Zhang, Z.22
Garchon, H.J.23
Bach, J.F.24
Rotter, J.I.25
She, J.X.26
Wang, C.Y.27
more..
-
19
-
-
33747648532
-
Evidence for the role of small ubiquitin-like modifier 4 as a general autoimmunity locus in the Japanese population
-
Tsurumaru M, Kawasaki E, Ida H, Migita K, Moriuchi A, Fukushima K, Fukushima T, Abiru N, Yamasaki H, Noso S, Ikegami H, Awata T, Sasaki H, Eguchi K. Evidence for the role of small ubiquitin-like modifier 4 as a general autoimmunity locus in the Japanese population. J Clin Endocrinol Metab 2006; 91:3138-43.
-
(2006)
J Clin Endocrinol Metab
, vol.91
, pp. 3138-3143
-
-
Tsurumaru, M.1
Kawasaki, E.2
Ida, H.3
Migita, K.4
Moriuchi, A.5
Fukushima, K.6
Fukushima, T.7
Abiru, N.8
Yamasaki, H.9
Noso, S.10
Ikegami, H.11
Awata, T.12
Sasaki, H.13
Eguchi, K.14
-
20
-
-
34347259280
-
Association of small ubiquitin-like modifier 4 (SUMO4) variant, located in IDDM5 locus, with type 2 diabetes in the Japanese population
-
Noso S, Fujisawa T, Kawabata Y, Asano K, Hiromine Y, Fukai A, Ogihara T, Ikegami H. Association of small ubiquitin-like modifier 4 (SUMO4) variant, located in IDDM5 locus, with type 2 diabetes in the Japanese population J Clin Endocrinol Metab 2007; 92:2358-62.
-
(2007)
J Clin Endocrinol Metab
, vol.92
, pp. 2358-2362
-
-
Noso, S.1
Fujisawa, T.2
Kawabata, Y.3
Asano, K.4
Hiromine, Y.5
Fukai, A.6
Ogihara, T.7
Ikegami, H.8
-
21
-
-
34047111206
-
SUMO4 M55V variant is associated with diabetic nephropathy in type 2 diabetes
-
Lin HY, Wang CL, Haiao PJ, Lu YC, Chen SY, Lin KD, Hsin SC, Hsieh MC, Shin SJ. SUMO4 M55V variant is associated with diabetic nephropathy in type 2 diabetes. Diabetes 2007, 56:1177-80.
-
(2007)
Diabetes
, vol.56
, pp. 1177-1180
-
-
Lin, H.Y.1
Wang, C.L.2
Haiao, P.J.3
Lu, Y.C.4
Chen, S.Y.5
Lin, K.D.6
Hsin, S.C.7
Hsieh, M.C.8
Shin, S.J.9
-
22
-
-
51249087940
-
SUMO4 gene polymorphisms in Chinese Han patients with Behcet's disease
-
Hou S, Yang P, Du L, Zhou H, Lin X, Liu X, Kijlstra A. SUMO4 gene polymorphisms in Chinese Han patients with Behcet's disease. Clin Immunol 2008; 129:170-5.
-
(2008)
Clin Immunol
, vol.129
, pp. 170-175
-
-
Hou, S.1
Yang, P.2
Du, L.3
Zhou, H.4
Lin, X.5
Liu, X.6
Kijlstra, A.7
-
23
-
-
3042740794
-
A 212-kb region on chromosome 6q25 containing the TAB2 gene is associated with susceptibility to type 1 diabetes
-
Owerbach D, Pina L, Gabbay KH. A 212-kb region on chromosome 6q25 containing the TAB2 gene is associated with susceptibility to type 1 diabetes. Diabetes 2004; 53:1890-3.
-
(2004)
Diabetes
, vol.53
, pp. 1890-1893
-
-
Owerbach, D.1
Pina, L.2
Gabbay, K.H.3
-
24
-
-
13944272690
-
Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes
-
Qu H, Bharaj B, Liu XQ, Curtis JA. Newhook LA. Paterson AD, Hudson TJ, Polychronakos C. Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes. Nat Genet 2005; 37:111-2.
-
(2005)
Nat Genet
, vol.37
, pp. 111-112
-
-
Qu, H.1
Bharaj, B.2
Liu, X.Q.3
Curtis, J.A.4
Newhook, L.A.5
Paterson, A.D.6
Hudson, T.J.7
Polychronakos, C.8
-
25
-
-
13944254773
-
Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes
-
Smyth DJ, Howson JM, Lowe CE, Walker NM, Lam AC, Nutland S, Hutchings J, Tuomilehto-Wolf E, Tuomilehto J, Guja C, Ionescu-Tirgoviste C, Undlien DE, Ronningen KS, Savage D, Dunger DB, Twells RC, McArdle WL, Strachan DP, Todd JA. Assessing the validity of the association between the SUMO4 M55V variant and risk of type 1 diabetes. Nat Genet 2005; 37:110-1.
-
(2005)
Nat Genet
, vol.37
, pp. 110-111
-
-
Smyth, D.J.1
Howson, J.M.2
Lowe, C.E.3
Walker, N.M.4
Lam, A.C.5
Nutland, S.6
Hutchings, J.7
Tuomilehto-Wolf, E.8
Tuomilehto, J.9
Guja, C.10
Ionescu-Tirgoviste, C.11
Undlien, D.E.12
Ronningen, K.S.13
Savage, D.14
Dunger, D.B.15
Twells, R.C.16
McArdle, W.L.17
Strachan, D.P.18
Todd, J.A.19
-
26
-
-
0026698645
-
Identification of the HLA-DRB1*04, -DRB1*07, and -DRB1*09 alleles by PCR amplification with sequence-specific primers (PCR-SSP) in 2 hours
-
Zetterquist H, Olerup O. Identification of the HLA-DRB1*04, -DRB1*07, and -DRB1*09 alleles by PCR amplification with sequence-specific primers (PCR-SSP) in 2 hours. Hum Immnol 1992; 34:64-74.
-
(1992)
Hum Immnol
, vol.34
, pp. 64-74
-
-
Zetterquist, H.1
Olerup, O.2
-
27
-
-
0027430877
-
HLA-DPB1 glutamate 69: A genetic marker of beryllium disease
-
Richeldi L, Sorrentino R, Saltini C. HLA-DPB1 glutamate 69: a genetic marker of beryllium disease. Science 1993; 262:242-4.
-
(1993)
Science
, vol.262
, pp. 242-244
-
-
Richeldi, L.1
Sorrentino, R.2
Saltini, C.3
-
28
-
-
13444269543
-
Haploview: Analysis and visualization of LD and haplotype maps
-
Barrett JC, Fry B, Maller J, Daly MJ. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 2005; 21:263-5.
-
(2005)
Bioinformatics
, vol.21
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
29
-
-
0036844521
-
Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphisms
-
Qin ZS, Niu T, Liu JS. Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphisms. Am J Hum Genet 2002; 71:1242-7.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1242-1247
-
-
Qin, Z.S.1
Niu, T.2
Liu, J.S.3
-
30
-
-
0035025345
-
Revised diagnostic criteria for Vogt-Koyanagi-Harada disease: Report of an international committee on nomenclature
-
Read RW, Holland GN, Rao NA, Tabbara KF, Ohno S, Arellanes-Garcia L, Pivetti-Pezzi P, Tessler HH, Usui M. Revised diagnostic criteria for Vogt-Koyanagi-Harada disease: report of an international committee on nomenclature. Am J Ophthalmol 2001; 131:647-52.
-
(2001)
Am J Ophthalmol
, vol.131
, pp. 647-652
-
-
Read, R.W.1
Holland, G.N.2
Rao, N.A.3
Tabbara, K.F.4
Ohno, S.5
Arellanes-Garcia, L.6
Pivetti-Pezzi, P.7
Tessler, H.H.8
Usui, M.9
-
31
-
-
50649095711
-
Associaiion study of NFKB1 and SUMO4 polymorphisms in Chinese patients with psoriasis vulgaris
-
Li H, Gao L, Shen Z, Li CY, Li K, Li M, Lv YJ, Li CX, Gao TW, Liu YF. Associaiion study of NFKB1 and SUMO4 polymorphisms in Chinese patients with psoriasis vulgaris. Arch Dermatol Res 2008; 300:425-33.
-
(2008)
Arch Dermatol Res
, vol.300
, pp. 425-433
-
-
Li, H.1
Gao, L.2
Shen, Z.3
Li, C.Y.4
Li, K.5
Li, M.6
Lv, Y.J.7
Li, C.X.8
Gao, T.W.9
Liu, Y.F.10
-
32
-
-
33644693805
-
Genetic heterogeneity in association of the SUMO4 M55V variant with susceptibility to type 1 diabetes
-
Noso S, Ikegami H, Fujisawa T, Kawabata Y, Asano K, Hiromine Y, Tsurumaru M, Sugihara S, Lee I, Kawasaki E, Awata T, Ogihara T. Genetic heterogeneity in association of the SUMO4 M55V variant with susceptibility to type 1 diabetes. Diabetes 2005; 54:3582-6.
-
(2005)
Diabetes
, vol.54
, pp. 3582-3586
-
-
Noso, S.1
Ikegami, H.2
Fujisawa, T.3
Kawabata, Y.4
Asano, K.5
Hiromine, Y.6
Tsurumaru, M.7
Sugihara, S.8
Lee, I.9
Kawasaki, E.10
Awata, T.11
Ogihara, T.12
-
33
-
-
0020624802
-
Choroidal neovascularization in long-standing case of Vogt-Koyanagi-Harada disease
-
Inomata H, Minei M, Taniguchi Y, Nishimura F. Choroidal neovascularization in long-standing case of Vogt-Koyanagi-Harada disease. Jpn J Ophthalmol 1983; 27:9-26.
-
(1983)
Jpn J Ophthalmol
, vol.27
, pp. 9-26
-
-
Inomata, H.1
Minei, M.2
Taniguchi, Y.3
Nishimura, F.4
-
34
-
-
0031173415
-
The association of HLA-DR4 gene subtypes with Vogt-Koyanagi-Harada syndrome
-
Xiao T, Jiang Y, You X. The association of HLA-DR4 gene subtypes with Vogt-Koyanagi-Harada syndrome. Zhonghua Yan Ke Za Zhi 1997; 33:268-71.
-
(1997)
Zhonghua Yan Ke Za Zhi
, vol.33
, pp. 268-271
-
-
Xiao, T.1
Jiang, Y.2
You, X.3
-
35
-
-
0029112428
-
Association between Vogt-Koyanagi-Harada syndrome and HLA-DR1 and -DR4 in Hispanic patients living in southern California
-
Weisz JM, Holland GN, Roer LN, Park MS, Yuge AJ, Moorthy RS, Forster DJ, Rao NA, Terasaki PI. Association between Vogt-Koyanagi-Harada syndrome and HLA-DR1 and -DR4 in Hispanic patients living in southern California. Ophthalmology 1995; 102:1012-5.
-
(1995)
Ophthalmology
, vol.102
, pp. 1012-1015
-
-
Weisz, J.M.1
Holland, G.N.2
Roer, L.N.3
Park, M.S.4
Yuge, A.J.5
Moorthy, R.S.6
Forster, D.J.7
Rao, N.A.8
Terasaki, P.I.9
|