-
1
-
-
0033828829
-
Recurrent germline mutation in MSH2 arises frequently de novo
-
Desai DC, Lockman JC, Chadwick RB, Gao X, Percesepe A, Evans DGR, Miyaki M, Yuen ST, Radice P, Maher ER, Wright FA, de la Chapelle A,. Recurrent germline mutation in MSH2 arises frequently de novo. J Med Genet 2000; 37: 646-52.
-
(2000)
J Med Genet
, vol.37
, pp. 646-652
-
-
Desai, D.C.1
Lockman, J.C.2
Chadwick, R.B.3
Gao, X.4
Percesepe, A.5
Evans, D.G.R.6
Miyaki, M.7
Yuen, S.T.8
Radice, P.9
Maher, E.R.10
Wright, F.A.11
De La Chapelle, A.12
-
2
-
-
0033039550
-
A common MSH2 mutation in English and North American HNPCC families: Origin, phenotypic expression, and sex specific differences in colorectal cancer
-
Froggatt NJ, Green J, Brassett C, Evans DG, Bishop DT, Kolodner R, Maher ER,. A common MSH2 mutation in English and North American HNPCC families: origin, phenotypic expression, and sex specific differences in colorectal cancer. J Med Genet 1999; 36: 97-102.
-
(1999)
J Med Genet
, vol.36
, pp. 97-102
-
-
Froggatt, N.J.1
Green, J.2
Brassett, C.3
Evans, D.G.4
Bishop, D.T.5
Kolodner, R.6
Maher, E.R.7
-
3
-
-
0036917758
-
The founder mutation MSH2*1906Gâ†'C is an important cause of Hereditary Non-Polyposis Colorectal Cancer in the Ashkenazi Jewish population
-
Foulkes WD, Thiffault I, Gruber SB, Horwitz M, Hamel N, Lee C, Shia J, Markowitz A, Figer A, Friedman E, Farber D, Greenwood CMT, et al. The founder mutation MSH2*1906Gâ†'C is an important cause of Hereditary Non-Polyposis Colorectal Cancer in the Ashkenazi Jewish population. Am J Hum Genet 2002; 71: 1395-412.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1395-1412
-
-
Foulkes, W.D.1
Thiffault, I.2
Gruber, S.B.3
Horwitz, M.4
Hamel, N.5
Lee, C.6
Shia, J.7
Markowitz, A.8
Figer, A.9
Friedman, E.10
Farber, D.11
Greenwood, C.M.T.12
-
4
-
-
0037730214
-
Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: High mutation detection rate among clinically selected families and charactrization of an American founder genomic deletion of the MSH2 gene
-
Wagner A, Barrows A, Wijnen JT, van der Klift H, Franken PF, Verkuijlen P, Nakagawa H, Geugien M, Jaghmohan-Changur S, Breukel C, Meijers-Heijboer H, Morreau H, et al. Molecular analysis of hereditary nonpolyposis colorectal cancer in the United States: high mutation detection rate among clinically selected families and charactrization of an American founder genomic deletion of the MSH2 gene. Am J Hum Genet 2003; 72: 1088-100.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1088-1100
-
-
Wagner, A.1
Barrows, A.2
Wijnen, J.T.3
Van Der Klift, H.4
Franken, P.F.5
Verkuijlen, P.6
Nakagawa, H.7
Geugien, M.8
Jaghmohan-Changur, S.9
Breukel, C.10
Meijers-Heijboer, H.11
Morreau, H.12
-
5
-
-
10744223648
-
A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States
-
Lynch HT, Coronel SM, Okimoto R, Hampel H, Sweet K, Lynch JF, Barrows A, Wijnen J, van der Klift H, Franken P, Wagner A, Fodde R, et al. A founder mutation of the MSH2 gene and hereditary nonpolyposis colorectal cancer in the United States. JAMA 2004; 291: 718-24.
-
(2004)
JAMA
, vol.291
, pp. 718-724
-
-
Lynch, H.T.1
Coronel, S.M.2
Okimoto, R.3
Hampel, H.4
Sweet, K.5
Lynch, J.F.6
Barrows, A.7
Wijnen, J.8
Van Der Klift, H.9
Franken, P.10
Wagner, A.11
Fodde, R.12
-
6
-
-
42049093195
-
Origins and prevalence of the American founder mutation of MSH2
-
Clendenning M, Baze MD, Sun S, Walsh K, Liyanarachchi S, Fix D, Schunemann V, Comeras I, Deacon M, Lynch JF, Gong G, Thomas BC, et al. Origins and prevalence of the American founder mutation of MSH2. Cancer Res 2008; 68: 2145-53.
-
(2008)
Cancer Res
, vol.68
, pp. 2145-2153
-
-
Clendenning, M.1
Baze, M.D.2
Sun, S.3
Walsh, K.4
Liyanarachchi, S.5
Fix, D.6
Schunemann, V.7
Comeras, I.8
Deacon, M.9
Lynch, J.F.10
Gong, G.11
Thomas, B.C.12
-
7
-
-
0032701335
-
Assessment of pathogenicity criteria for constitutional missense mutations of the hereditary nonpolyposis colorectal cancer genes MLH1 and MSH2
-
Genuardi M, Carrara S, Anti M, Ponz de LeÃn M, Viel A,. Assessment of pathogenicity criteria for constitutional missense mutations of the hereditary nonpolyposis colorectal cancer genes MLH1 and MSH2. Eur J Hum Genet 1999; 7: 778-82.
-
(1999)
Eur J Hum Genet
, vol.7
, pp. 778-782
-
-
Genuardi, M.1
Carrara, S.2
Anti, M.3
Ponz De Leãn, M.4
Viel, A.5
-
8
-
-
0000151696
-
Hereditary nonpolyposis colorectal cancer: An approach to the selection of candidates to genetic testing based on clinical and molecular characteristics
-
Viel A, Genuardi M, Lucci-Cordisco E, Capozzi E, Rovella V, Fornasarig M, Ponz de LeÃn M, Anti M, Pedroni M, Bellacosa A, Percesepe A, Covino M, et al. Hereditary nonpolyposis colorectal cancer: an approach to the selection of candidates to genetic testing based on clinical and molecular characteristics. Community Genet 1998; 1: 229-36.
-
(1998)
Community Genet
, vol.1
, pp. 229-236
-
-
Viel, A.1
Genuardi, M.2
Lucci-Cordisco, E.3
Capozzi, E.4
Rovella, V.5
Fornasarig, M.6
Ponz De Leãn, M.7
Anti, M.8
Pedroni, M.9
Bellacosa, A.10
Percesepe, A.11
Covino, M.12
-
9
-
-
33749029656
-
Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: A report by the German HNPCC Consortium
-
Goecke T, Schulmann K, Engel C, Holinski-Feder E, Pagenstecher C, Schackert HK, Kloor M, Kunstmann E, Vogelsang H, Keller G, Dietmaier W, Mangold E, et al. Genotype-phenotype comparison of German MLH1 and MSH2 mutation carriers clinically affected with Lynch syndrome: a report by the German HNPCC Consortium. J Clin Oncol 2006; 24: 4285-92.
-
(2006)
J Clin Oncol
, vol.24
, pp. 4285-4292
-
-
Goecke, T.1
Schulmann, K.2
Engel, C.3
Holinski-Feder, E.4
Pagenstecher, C.5
Schackert, H.K.6
Kloor, M.7
Kunstmann, E.8
Vogelsang, H.9
Keller, G.10
Dietmaier, W.11
Mangold, E.12
-
10
-
-
0029164415
-
In vitro transcription/translation assay for the screening of hMLH1 and hMSH2 mutations in familial colon cancer
-
Luce MC, Marra G, Chauhan DP, Laghi L, Carethers JM, Cherian SP, Hawn M, Binnie CG, Kam-Morgan LN, Cayouette MC,. In vitro transcription/translation assay for the screening of hMLH1 and hMSH2 mutations in familial colon cancer. Gastroenterology 1995; 109: 1368-74.
-
(1995)
Gastroenterology
, vol.109
, pp. 1368-1374
-
-
Luce, M.C.1
Marra, G.2
Chauhan, D.P.3
Laghi, L.4
Carethers, J.M.5
Cherian, S.P.6
Hawn, M.7
Binnie, C.G.8
Kam-Morgan, L.N.9
Cayouette, M.C.10
-
11
-
-
0033591855
-
Interpretation of genetic test results for hereditary nonpolyposis colorectal cancer: Implications for clinical predisposition testing
-
Syngal S, Fox EA, Li C, Dovidio M, Eng C, Kolodner RD, Garber JE,. Interpretation of genetic test results for hereditary nonpolyposis colorectal cancer: implications for clinical predisposition testing. JAMA 1999; 282: 247-53.
-
(1999)
JAMA
, vol.282
, pp. 247-253
-
-
Syngal, S.1
Fox, E.A.2
Li, C.3
Dovidio, M.4
Eng, C.5
Kolodner, R.D.6
Garber, J.E.7
-
12
-
-
33747871345
-
Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients
-
Hampel H, Frankel W, Panescu J, Lockman J, Sotamaa K, Fix D, Comeras I, La Jeunesse J, Nakagawa H, Westman JA, Prior TW, Clendenning M, et al. Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients. Cancer Res 2006; 66: 7810-7.
-
(2006)
Cancer Res
, vol.66
, pp. 7810-7817
-
-
Hampel, H.1
Frankel, W.2
Panescu, J.3
Lockman, J.4
Sotamaa, K.5
Fix, D.6
Comeras, I.7
La Jeunesse, J.8
Nakagawa, H.9
Westman, J.A.10
Prior, T.W.11
Clendenning, M.12
-
13
-
-
0029851496
-
Age and origin of two common MLH1 mutations predisposing to hereditary colon cancer
-
Moisio AL, Sistonen P, Weissenbach J, de la Chapelle A, Peltomäki P,. Age and origin of two common MLH1 mutations predisposing to hereditary colon cancer. Am J Hum Genet 1996; 59: 1243-51.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 1243-1251
-
-
Moisio, A.L.1
Sistonen, P.2
Weissenbach, J.3
De La Chapelle, A.4
Peltomäki, P.5
-
14
-
-
0036300177
-
DMLE+: Bayesian linkage disequilibrium gene mapping
-
Reeve JP, Rannala B,. DMLE+: Bayesian linkage disequilibrium gene mapping. Bioinformatics 2002; 18: 894-5.
-
(2002)
Bioinformatics
, vol.18
, pp. 894-895
-
-
Reeve, J.P.1
Rannala, B.2
-
15
-
-
0032735986
-
Population growth of human y chromosomes: A study of y chromosome microsatellites
-
Pritchard JK, Seielstad MT, Perez-Lezaun A, Feldman MW,. Population growth of human Y chromosomes: a study of Y chromosome microsatellites. Mol Biol Evol 1999; 16: 1791-8.
-
(1999)
Mol Biol Evol
, vol.16
, pp. 1791-1798
-
-
Pritchard, J.K.1
Seielstad, M.T.2
Perez-Lezaun, A.3
Feldman, M.W.4
-
16
-
-
45249083654
-
A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome
-
Clendenning M, Senter L, Hampel H, Robinson KL, Sun S, Buchanan D, Walsh MD, Nilbert M, Green J, Potter J, Lindblom A, de la Chapelle A,. A frame-shift mutation of PMS2 is a widespread cause of Lynch syndrome. J Med Genet 2008; 45: 340-5.
-
(2008)
J Med Genet
, vol.45
, pp. 340-345
-
-
Clendenning, M.1
Senter, L.2
Hampel, H.3
Robinson, K.L.4
Sun, S.5
Buchanan, D.6
Walsh, M.D.7
Nilbert, M.8
Green, J.9
Potter, J.10
Lindblom, A.11
De La Chapelle, A.12
-
17
-
-
2942726191
-
Estimating the age of rare disease mutations: The example of Triple-A syndrome
-
Genin E, Tullio-Pelet A, Begeot F, Lyonnet S, Abel L,. Estimating the age of rare disease mutations: the example of Triple-A syndrome. J Med Genet 2004; 41: 445-9.
-
(2004)
J Med Genet
, vol.41
, pp. 445-449
-
-
Genin, E.1
Tullio-Pelet, A.2
Begeot, F.3
Lyonnet, S.4
Abel, L.5
-
18
-
-
35148901553
-
Comment on: Screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients
-
Hampel H, Panescu J, Lockman J, Sotamaa K, Fix D, Comeras I, LaJeunesse J, Nakagawa H, Westman JA, Prior TW, Clendenning M, de la Chapelle A, et al. Comment on: screening for Lynch syndrome (hereditary nonpolyposis colorectal cancer) among endometrial cancer patients. Cancer Res 2007; 67: 9603.
-
(2007)
Cancer Res
, vol.67
, pp. 9603
-
-
Hampel, H.1
Panescu, J.2
Lockman, J.3
Sotamaa, K.4
Fix, D.5
Comeras, I.6
Lajeunesse, J.7
Nakagawa, H.8
Westman, J.A.9
Prior, T.W.10
Clendenning, M.11
De La Chapelle, A.12
-
19
-
-
57449097359
-
Feasibility of screening for Lynch syndrome among colorectal cancer patients
-
Hampel H, Frankel WL, Martin E, Arnold M, Khanduja K, Kuebler P, Clendenning M, Sotamaa K, Prior T, Westman J, Panescu J, Fix D, et al. Feasibility of screening for Lynch syndrome among colorectal cancer patients. J Clin Oncol 2008; 26: 5783-8.
-
(2008)
J Clin Oncol
, vol.26
, pp. 5783-5788
-
-
Hampel, H.1
Frankel, W.L.2
Martin, E.3
Arnold, M.4
Khanduja, K.5
Kuebler, P.6
Clendenning, M.7
Sotamaa, K.8
Prior, T.9
Westman, J.10
Panescu, J.11
Fix, D.12
-
20
-
-
0034677493
-
Conversion of diploidy to haploidy
-
Yan H, Papadopoulos N, Marra G, Perrera C, Jiricny J, Boland CR, Lynch HT, Chadwick RB, de la Chapelle A, Berg K, Eshleman JR, Yuan W, et al. Conversion of diploidy to haploidy. Nature 2000; 403: 723-4.
-
(2000)
Nature
, vol.403
, pp. 723-724
-
-
Yan, H.1
Papadopoulos, N.2
Marra, G.3
Perrera, C.4
Jiricny, J.5
Boland, C.R.6
Lynch, H.T.7
Chadwick, R.B.8
De La Chapelle, A.9
Berg, K.10
Eshleman, J.R.11
Yuan, W.12
-
21
-
-
1642416883
-
Genetic testing among high-risk individuals in families with hereditary nonpolyposis colorectal cancer
-
Ponz de Leon M, Benatti P, Di Gregorio C, Pedroni M, Losi L, Genuardi M, Viel A, Fornasarig M, Lucci-Cordisco E, Anti M, Ponti G, Borghi F, et al. Genetic testing among high-risk individuals in families with hereditary nonpolyposis colorectal cancer. Br J Cancer 2004; 90: 882-7.
-
(2004)
Br J Cancer
, vol.90
, pp. 882-887
-
-
Ponz De Leon, M.1
Benatti, P.2
Di Gregorio, C.3
Pedroni, M.4
Losi, L.5
Genuardi, M.6
Viel, A.7
Fornasarig, M.8
Lucci-Cordisco, E.9
Anti, M.10
Ponti, G.11
Borghi, F.12
-
22
-
-
23244452266
-
Functional significance and clinical phenotype of nontruncating mismatch repair variants of MLH1
-
Raevaara TE, Korhonen MK, Lohi H, Hampel H, Lynch E, Lönnqvist KE, Holinski-Feder E, Sutter C, McKinnon W, Duraisamy S, Gerdes A-M, Peltomäki P, et al. Functional significance and clinical phenotype of nontruncating mismatch repair variants of MLH1. Gastroenterology 2005; 129: 537-49.
-
(2005)
Gastroenterology
, vol.129
, pp. 537-549
-
-
Raevaara, T.E.1
Korhonen, M.K.2
Lohi, H.3
Hampel, H.4
Lynch, E.5
Lönnqvist, K.E.6
Holinski-Feder, E.7
Sutter, C.8
McKinnon, W.9
Duraisamy, S.10
Gerdes, A.-M.11
Peltomäki, P.12
-
23
-
-
34250344873
-
Functional analysis of human MLH1 variants using yeast and in vitro mismatch repair assays
-
Takahashi M, Shimodaira H, Andreutti-Zaugg C, Iggo R, Kolodner RD, Ishioka C,. Functional analysis of human MLH1 variants using yeast and in vitro mismatch repair assays. Cancer Res 2007; 67: 4595-604.
-
(2007)
Cancer Res
, vol.67
, pp. 4595-4604
-
-
Takahashi, M.1
Shimodaira, H.2
Andreutti-Zaugg, C.3
Iggo, R.4
Kolodner, R.D.5
Ishioka, C.6
-
24
-
-
77950452745
-
Functional analysis of human mismatch repair gene mutations identifies weak alleles and polymorphisms capable of polygenic interactions
-
Martinez SL, Kolodner RD,. Functional analysis of human mismatch repair gene mutations identifies weak alleles and polymorphisms capable of polygenic interactions. Proc Natl Acad Sci U S A 2010; 107: 5070-5.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 5070-5075
-
-
Martinez, S.L.1
Kolodner, R.D.2
-
25
-
-
77149143820
-
A cell-free assay for the functional analysis of variants of the mismatch repair protein MLH1
-
Drost M, Zonneveld JB, van Dijk L, Morreau H, Tops CM, Vasen HF, Wijnen JT, de Wind N,. A cell-free assay for the functional analysis of variants of the mismatch repair protein MLH1. Hum Mutat 2010; 31: 247-53.
-
(2010)
Hum Mutat
, vol.31
, pp. 247-253
-
-
Drost, M.1
Zonneveld, J.B.2
Van Dijk, L.3
Morreau, H.4
Tops, C.M.5
Vasen, H.F.6
Wijnen, J.T.7
De Wind, N.8
-
26
-
-
79951575821
-
Integrated analysis of unclassified variants in mismatch repair genes
-
Pastrello C, Pin E, Marroni F, Bedin C, Fornasarig M, Tibiletti MG, Oliani C, Ponz de Leon M, Urso ED, Della Puppa L, Agostini M, Viel A,. Integrated analysis of unclassified variants in mismatch repair genes. Genet Med 2011; 13: 115-24.
-
(2011)
Genet Med
, vol.13
, pp. 115-124
-
-
Pastrello, C.1
Pin, E.2
Marroni, F.3
Bedin, C.4
Fornasarig, M.5
Tibiletti, M.G.6
Oliani, C.7
Ponz De Leon, M.8
Urso, E.D.9
Della Puppa, L.10
Agostini, M.11
Viel, A.12
-
27
-
-
0030997158
-
Mutational analysis of MLH1 and MSH2 in 25 prospectively-acquired RER+ endometrial cancers
-
Kowalski LD, Mutch DG, Herzog TJ, Rader JS, Goodfellow PJ,. Mutational analysis of MLH1 and MSH2 in 25 prospectively-acquired RER+ endometrial cancers. Genes Chromosomes Cancer 1997; 18: 219-27.
-
(1997)
Genes Chromosomes Cancer
, vol.18
, pp. 219-227
-
-
Kowalski, L.D.1
Mutch, D.G.2
Herzog, T.J.3
Rader, J.S.4
Goodfellow, P.J.5
-
28
-
-
0033962257
-
Extensive molecular screening for hereditary non-polyposis colorectal cancer
-
Dieumegard B, Grandjouan S, Sabourin JC, Le Bihan ML, LefrÃ̈re I, Bellefqih, Pignon JP, Rougier P, Lasser P, Bénard J, Couturier D, Bressac-de Paillerets B,. Extensive molecular screening for hereditary non-polyposis colorectal cancer. Br J Cancer 2000; 82: 871-80.
-
(2000)
Br J Cancer
, vol.82
, pp. 871-880
-
-
Dieumegard, B.1
Grandjouan, S.2
Sabourin, J.C.3
Le Bihan, M.L.4
Lefrã̈re, I.5
Bellefqih6
Pignon, J.P.7
Rougier, P.8
Lasser, P.9
Bénard, J.10
Couturier, D.11
Bressac-De Paillerets, B.12
-
29
-
-
77957896955
-
Unique DNA repair gene variations and potential associations with the primary antibody deficiency syndromes IgAD and CVID
-
Offer SM, Pan-Hammarström Q, Hammarström L, Harris RS,. Unique DNA repair gene variations and potential associations with the primary antibody deficiency syndromes IgAD and CVID. PLoS One 2010; 5: e12260.
-
(2010)
PLoS One
, vol.5
-
-
Offer, S.M.1
Pan-Hammarström, Q.2
Hammarström, L.3
Harris, R.S.4
-
30
-
-
40549109545
-
Classification of ambiguous mutations in DNA mismatch repair genes identified in a population-based study of colorectal cancer
-
Barnetson RA, Cartwright N, van Vliet A, Haq N, Drew K, Farrington S, Williams N, Warner J, Campbell H, Porteous ME, Dunlop MG,. Classification of ambiguous mutations in DNA mismatch repair genes identified in a population-based study of colorectal cancer. Hum Mutat 2008; 29: 367-74.
-
(2008)
Hum Mutat
, vol.29
, pp. 367-374
-
-
Barnetson, R.A.1
Cartwright, N.2
Van Vliet, A.3
Haq, N.4
Drew, K.5
Farrington, S.6
Williams, N.7
Warner, J.8
Campbell, H.9
Porteous, M.E.10
Dunlop, M.G.11
-
31
-
-
0035071957
-
A new statistical method for haplotype reconstruction from population data
-
Stephens M, Smith NJ, Donnelly P,. A new statistical method for haplotype reconstruction from population data. Am J Hum Genet 2001; 68: 978-89.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 978-989
-
-
Stephens, M.1
Smith, N.J.2
Donnelly, P.3
-
32
-
-
0242691208
-
A comparison of bayesian methods for haplotype reconstruction from population genotype data
-
Stephens M, Donnelly P,. A comparison of bayesian methods for haplotype reconstruction from population genotype data. Am J Hum Genet 2003; 73: 1162-9.
-
(2003)
Am J Hum Genet
, vol.73
, pp. 1162-1169
-
-
Stephens, M.1
Donnelly, P.2
-
33
-
-
0028845693
-
Founding mutations and Alu-mediated recombination in hereditary colon cancer
-
Nyström-Lahti M, Kristo P, Nicolaides NC, Chang SY, Aaltonen LA, Moisio AL, Järvinen HJ, Mecklin JP, Kinzler KW, Vogelstein B,. Founding mutations and Alu-mediated recombination in hereditary colon cancer. Nat Med 1995; 1: 1203-6.
-
(1995)
Nat Med
, vol.1
, pp. 1203-1206
-
-
Nyström-Lahti, M.1
Kristo, P.2
Nicolaides, N.C.3
Chang, S.Y.4
Aaltonen, L.A.5
Moisio, A.L.6
Järvinen, H.J.7
Mecklin, J.P.8
Kinzler, K.W.9
Vogelstein, B.10
-
34
-
-
22944433733
-
Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer
-
Mangold E, Pagenstecher C, Friedl W, Mathiak M, Buettner R, Engel C, Loeffler M, Holinski-Feder E, Müller-Koch Y, Keller G, Schackert HK, Krüger S, et al. Spectrum and frequencies of mutations in MSH2 and MLH1 identified in 1,721 German families suspected of hereditary nonpolyposis colorectal cancer. Int J Cancer 2005; 116: 692-702.
-
(2005)
Int J Cancer
, vol.116
, pp. 692-702
-
-
Mangold, E.1
Pagenstecher, C.2
Friedl, W.3
Mathiak, M.4
Buettner, R.5
Engel, C.6
Loeffler, M.7
Holinski-Feder, E.8
Müller-Koch, Y.9
Keller, G.10
Schackert, H.K.11
Krüger, S.12
|