-
1
-
-
0035159678
-
Mutation screening at the RNA level of the STK11/LKB1 gene in the Peutz-Jeghers syndrome reveals complex splicing abnormalities and a novel mRNA isoform (STK11 c.597^598insIVS4)
-
Abed AA, Gunther K, Kraus C, Hohenberger W, Ballhausen WG (2001) Mutation screening at the RNA level of the STK11/LKB1 gene in the Peutz-Jeghers syndrome reveals complex splicing abnormalities and a novel mRNA isoform (STK11 c.597^598insIVS4). Hum Mutat 18: 397-410
-
(2001)
Hum Mutat
, vol.18
, pp. 397-410
-
-
Abed, A.A.1
Gunther, K.2
Kraus, C.3
Hohenberger, W.4
Ballhausen, W.G.5
-
2
-
-
0032054770
-
Low frequency of somatic mutations in the LKB1/Peutz-Jeghers syndrome gene in sporadic breast cancer
-
Bignell GR, Barfoot R, Seal S, Collins N, Warren W, Stratton MR (1998) Low frequency of somatic mutations in the LKB1/Peutz-Jeghers syndrome gene in sporadic breast cancer. Cancer Res 58: 1384-1386
-
(1998)
Cancer Res
, vol.58
, pp. 1384-1386
-
-
Bignell, G.R.1
Barfoot, R.2
Seal, S.3
Collins, N.4
Warren, W.5
Stratton, M.R.6
-
3
-
-
0033923499
-
Genetic heterogeneity in Peutz-Jeghers syndrome
-
Boardman LA, Couch FJ, Burgart LJ, Schwartz D, Berry R, McDonnell SK, Schaid DJ, Hartmann LC, Schroeder JJ, Stratakis CA, Thibodeau SN (2000) Genetic heterogeneity in Peutz-Jeghers syndrome. Hum Mut 16: 23-30
-
(2000)
Hum Mut
, vol.16
, pp. 23-30
-
-
Boardman, L.A.1
Couch, F.J.2
Burgart, L.J.3
Schwartz, D.4
Berry, R.5
McDonnell, S.K.6
Schaid, D.J.7
Hartmann, L.C.8
Schroeder, J.J.9
Stratakis, C.A.10
Thibodeau, S.N.11
-
4
-
-
0020443317
-
Peutz-Jeghers syndrome. A clinicopathological study of a large family with a 27-year follow-up
-
Burdick D, Prior JT (1982) Peutz-Jeghers syndrome. A clinicopathological study of a large family with a 27-year follow-up. Cancer 50: 2139-2146
-
(1982)
Cancer
, vol.50
, pp. 2139-2146
-
-
Burdick, D.1
Prior, J.T.2
-
5
-
-
0025970813
-
An aromatase-producing sex-cord tumor resulting in prepurbertal gynaecomastia
-
Coen P, Kulin H, Ballantine T, Zaino R, Frauenhoffer E, Boal D, Inkster S, Brodie A, Santen R (1991) An aromatase-producing sex-cord tumor resulting in prepurbertal gynaecomastia. New Engl J Med 324: 317-322
-
(1991)
New Engl J Med
, vol.324
, pp. 317-322
-
-
Coen, P.1
Kulin, H.2
Ballantine, T.3
Zaino, R.4
Frauenhoffer, E.5
Boal, D.6
Inkster, S.7
Brodie, A.8
Santen, R.9
-
6
-
-
0034141636
-
LKB1, a novel serine/threonine protein kinase and potential tumour suppressor, is phosphorylated by cAMP-dependent protein kinase (PKA) and prenylated in vivo
-
Collins SP, Reoma JL, Gamm DM, Uhler MD (2000) LKB1, a novel serine/threonine protein kinase and potential tumour suppressor, is phosphorylated by cAMP-dependent protein kinase (PKA) and prenylated in vivo. Biochem J 345: 673-680
-
(2000)
Biochem J
, vol.345
, pp. 673-680
-
-
Collins, S.P.1
Reoma, J.L.2
Gamm, D.M.3
Uhler, M.D.4
-
7
-
-
0024238366
-
Peutz-Jeghers syndrome: A clinicopathological survey of the 'Harrisburg family' with a 49-year follow-up
-
Foley TR, McGarrity TJ, Abt AB (1998) Peutz-Jeghers syndrome: a clinicopathological survey of the 'Harrisburg family' with a 49-year follow-up. Gastroenterology 95: 1535-1540
-
(1998)
Gastroenterology
, vol.95
, pp. 1535-1540
-
-
Foley, T.R.1
McGarrity, T.J.2
Abt, A.B.3
-
8
-
-
0027433113
-
Conformation-sensitive gel electrophoresis for rapid detection of single base differences in double stranded PCR products and DNA fragments: Evidence for solvent induced bends in DNA heteroduplexes
-
Ganguly A, Rock MJ, Prockop DJ (1993) Conformation-sensitive gel electrophoresis for rapid detection of single base differences in double stranded PCR products and DNA fragments: evidence for solvent induced bends in DNA heteroduplexes. Proc Natl Acad Sci USA 90: 10325-10329
-
(1993)
Proc Natl Acad Sci USA
, vol.90
, pp. 10325-10329
-
-
Ganguly, A.1
Rock, M.J.2
Prockop, D.J.3
-
9
-
-
0034464147
-
Very high risk of cancer in familial Peutz-Jeghers syndrome
-
Giardello FM, Brensinger JD, Tersmette AC, Goodman SN, Petersen GM, Booker SV, Cruz-Correa M, Offerhaus GJA (2000) Very high risk of cancer in familial Peutz-Jeghers syndrome. Gastroenterology 119: 1447-1453
-
(2000)
Gastroenterology
, vol.119
, pp. 1447-1453
-
-
Giardello, F.M.1
Brensinger, J.D.2
Tersmette, A.C.3
Goodman, S.N.4
Petersen, G.M.5
Booker, S.V.6
Cruz-Correa, M.7
Offerhaus, G.J.A.8
-
10
-
-
0023192463
-
Increased risk of cancer in the Peutz-Jeghers syndrome
-
Giardello FM, Welsh SB, Hamilton SR, Offerhaus GJA, Gittelsohn AM, Booker SV, Krush AJ, Yardley JH, Luk GD (1987) Increased risk of cancer in the Peutz-Jeghers syndrome. N Engl J Med 316: 1511-1514
-
(1987)
N Engl J Med
, vol.316
, pp. 1511-1514
-
-
Giardello, F.M.1
Welsh, S.B.2
Hamilton, S.R.3
Offerhaus, G.J.A.4
Gittelsohn, A.M.5
Booker, S.V.6
Krush, A.J.7
Yardley, J.H.8
Luk, G.D.9
-
11
-
-
0032403068
-
Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome
-
Gruber SB, Entius MM, Petersen GM, Laken SJ, Longo PA, Boyer R, Levin AM, Mujumdar UJ, Trent JM, Kinzler KW, Vogelstein B, Hamilton SR, Polymeropoulos MH, Offerhaus GJ, Giardello FM (1998) Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome. Cancer Res 58: 5267-5270
-
(1998)
Cancer Res
, vol.58
, pp. 5267-5270
-
-
Gruber, S.B.1
Entius, M.M.2
Petersen, G.M.3
Laken, S.J.4
Longo, P.A.5
Boyer, R.6
Levin, A.M.7
Mujumdar, U.J.8
Trent, J.M.9
Kinzler, K.W.10
Vogelstein, B.11
Hamilton, S.R.12
Polymeropoulos, M.H.13
Offerhaus, G.J.14
Giardello, F.M.15
-
12
-
-
0032495530
-
A Serine/threonine kinase gene defective in Peutz-Jeghers syndrome
-
Hemminki A, Markie D, Tomlinson I, Avizienyte E, Roth S, Loukola A, Bignell G, Warren W, Aminoff M, Hoglund P, Jarvinen H, Kristo P, Pelin K, Ridanpaa M, Salovaara R, Toro T, Bodmer W, Olschwang S, Olsen AS, Stratton MR, de la Chapelle A, Aaltonen LA (1998) A Serine/threonine kinase gene defective in Peutz-Jeghers syndrome. Nature 391: 184-187
-
(1998)
Nature
, vol.391
, pp. 184-187
-
-
Hemminki, A.1
Markie, D.2
Tomlinson, I.3
Avizienyte, E.4
Roth, S.5
Loukola, A.6
Bignell, G.7
Warren, W.8
Aminoff, M.9
Hoglund, P.10
Jarvinen, H.11
Kristo, P.12
Pelin, K.13
Ridanpaa, M.14
Salovaara, R.15
Toro, T.16
Bodmer, W.17
Olschwang, S.18
Olsen, A.S.19
Stratton, M.R.20
De La Chapelle, A.21
Aaltonen, L.A.22
more..
-
13
-
-
0031012344
-
Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridisation and targeted linkage analysis
-
Hemminki A, Tomlinson I, Markie D, Jarvinen H, Sistonen P, Bjorkqvist AM, Knuutila S, Salovaara R, Bodmer W, Shibata D, de la Chapelle A, Aaltonen LA (1997) Localization of a susceptibility locus for Peutz-Jeghers syndrome to 19p using comparative genomic hybridisation and targeted linkage analysis. Nat Genet 15: 87-90
-
(1997)
Nat Genet
, vol.15
, pp. 87-90
-
-
Hemminki, A.1
Tomlinson, I.2
Markie, D.3
Jarvinen, H.4
Sistonen, P.5
Bjorkqvist, A.M.6
Knuutila, S.7
Salovaara, R.8
Bodmer, W.9
Shibata, D.10
De La Chapelle, A.11
Aaltonen, L.A.12
-
14
-
-
0031974516
-
Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase
-
Jenne DE, Reimann H, Nezu J, Friedel W, Loff S, Jeschke R, Muller O, Back W, Zimmer M (1998) Peutz-Jeghers syndrome is caused by mutations in a novel serine threonine kinase. Nat Genet 18: 38-43
-
(1998)
Nat Genet
, vol.18
, pp. 38-43
-
-
Jenne, D.E.1
Reimann, H.2
Nezu, J.3
Friedel, W.4
Loff, S.5
Jeschke, R.6
Muller, O.7
Back, W.8
Zimmer, M.9
-
15
-
-
0032876595
-
STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients
-
Jiang CY, Esufali S, Berk T, Gallinger S, Cohen Z, Tobi M, Redston M, Bapat B (1999) STK11/LKB1 germline mutations are not identified in most Peutz-Jeghers syndrome patients. Clin Genet 56: 136-141
-
(1999)
Clin Genet
, vol.56
, pp. 136-141
-
-
Jiang, C.Y.1
Esufali, S.2
Berk, T.3
Gallinger, S.4
Cohen, Z.5
Tobi, M.6
Redston, M.7
Bapat, B.8
-
16
-
-
0032604662
-
Peutz-Jeghers syndrome: Four novel inactivating germline mutations in the STK11 gene
-
Kruse R, Uhlhaas S, Lamberti C, Keller KM, Jackisch C, Steinhard J, Knöpfle G, Loff S, Back W, Stolte M, Jungck M, Propping P, Friedl W, Jenne DE (1999) Peutz-Jeghers syndrome: four novel inactivating germline mutations in the STK11 gene. Hum Mut 13: 257-258
-
(1999)
Hum Mut
, vol.13
, pp. 257-258
-
-
Kruse, R.1
Uhlhaas, S.2
Lamberti, C.3
Keller, K.M.4
Jackisch, C.5
Steinhard, J.6
Knöpfle, G.7
Loff, S.8
Back, W.9
Stolte, M.10
Jungck, M.11
Propping, P.12
Friedl, W.13
Jenne, D.E.14
-
17
-
-
0032471851
-
Loss of LKB1 kinase activity in Peutz-Jeghers syndrome and evidence for allelic and locus heterogeneity
-
Mehenni H, Gehrig C, Nezu J, Oku A, Shimane M, Rossier C, Guex N, Blouin JL, Scott HS, Antonarakis SE (1998) Loss of LKB1 kinase activity in Peutz-Jeghers syndrome and evidence for allelic and locus heterogeneity. Am J Hum Genet 63: 1641-1650
-
(1998)
Am J Hum Genet
, vol.63
, pp. 1641-1650
-
-
Mehenni, H.1
Gehrig, C.2
Nezu, J.3
Oku, A.4
Shimane, M.5
Rossier, C.6
Guex, N.7
Blouin, J.L.8
Scott, H.S.9
Antonarakis, S.E.10
-
18
-
-
0033692749
-
Somatic mutations of LKB1 and beta-catenin genes in gastrointestinal polyps from patients with Peutz-Jeghers syndrome
-
Miyaki M, Iijima T, Hosono K, Ishii R, Yasuno M, Mori T, Toi M, Hishima T, Shitara N, Tamura K, Utsunomiya J, Kobayashi N, Kuroki T, Iwama T (2000) Somatic mutations of LKB1 and beta-catenin genes in gastrointestinal polyps from patients with Peutz-Jeghers syndrome. Cancer Res 60: 6311-6313
-
(2000)
Cancer Res
, vol.60
, pp. 6311-6313
-
-
Miyaki, M.1
Iijima, T.2
Hosono, K.3
Ishii, R.4
Yasuno, M.5
Mori, T.6
Toi, M.7
Hishima, T.8
Shitara, N.9
Tamura, K.10
Utsunomiya, J.11
Kobayashi, N.12
Kuroki, T.13
Iwama, T.14
-
19
-
-
0036644884
-
Evaluation of candidate genes MAP2K4, MADH4, ACVR1B, and BRCA2 in familial pancreatic cancer
-
Murphy KM, Brune KA, Griffin C, Sollenberger JE, Petersen GM, Bansal R, Hruban RH, Kern SE (2002) Evaluation of candidate genes MAP2K4, MADH4, ACVR1B, and BRCA2 in familial pancreatic cancer. Cancer Res 62: 3789-3793
-
(2002)
Cancer Res
, vol.62
, pp. 3789-3793
-
-
Murphy, K.M.1
Brune, K.A.2
Griffin, C.3
Sollenberger, J.E.4
Petersen, G.M.5
Bansal, R.6
Hruban, R.H.7
Kern, S.E.8
-
20
-
-
0031662147
-
Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome
-
Nakagawa H, Koyama K, Miyoshi Y, Ando H, Baba S, Watatani M, Yasutomi M, Matsuura N, Monden M, Nakamura Y (1998) Nine novel germline mutations of STK11 in ten families with Peutz-Jeghers syndrome. Hum Genet 103: 168-172
-
(1998)
Hum Genet
, vol.103
, pp. 168-172
-
-
Nakagawa, H.1
Koyama, K.2
Miyoshi, Y.3
Ando, H.4
Baba, S.5
Watatani, M.6
Yasutomi, M.7
Matsuura, N.8
Monden, M.9
Nakamura, Y.10
-
21
-
-
0034988818
-
Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma
-
Olschwang S, Boisson C, Thomas G (2001) Peutz-Jeghers families unlinked to STK11/LKB1 gene mutations are highly predisposed to primitive biliary adenocarcinoma. J Med Genet 38: 356-360
-
(2001)
J Med Genet
, vol.38
, pp. 356-360
-
-
Olschwang, S.1
Boisson, C.2
Thomas, G.3
-
22
-
-
14444272759
-
STK11/LKB1 mutations in Peutz-Jeghers syndrome and sporadic colon cancer
-
Resta N, Simone C, Mareni C, Montera M, Gentile M, Susca F, Gristina R, Pozzi S, Bertario L, Bufo P, Carlomagno N, Ingrosso M, Rossini FP, Tenconi R, Guanti G (1998) STK11/LKB1 mutations in Peutz-Jeghers syndrome and sporadic colon cancer. Cancer Res 58: 4799-4801
-
(1998)
Cancer Res
, vol.58
, pp. 4799-4801
-
-
Resta, N.1
Simone, C.2
Mareni, C.3
Montera, M.4
Gentile, M.5
Susca, F.6
Gristina, R.7
Pozzi, S.8
Bertario, L.9
Bufo, P.10
Carlomagno, N.11
Ingrosso, M.12
Rossini, F.P.13
Tenconi, R.14
Guanti, G.15
-
23
-
-
0020963860
-
Peutz-Jeghers syndrome associated with precocious puberty
-
Sohl HM, Azoury RS, Najjar SS (1983) Peutz-Jeghers syndrome associated with precocious puberty. J Pediatr 103: 593-595
-
(1983)
J Pediatr
, vol.103
, pp. 593-595
-
-
Sohl, H.M.1
Azoury, R.S.2
Najjar, S.S.3
-
24
-
-
0014932888
-
Peutz-Jeghers syndrome and ureteral polyposis
-
Sommerhaug RG, Mason T (1970) Peutz-Jeghers syndrome and ureteral polyposis. J Am Med Assoc 211: 120-122
-
(1970)
J Am Med Assoc
, vol.211
, pp. 120-122
-
-
Sommerhaug, R.G.1
Mason, T.2
-
25
-
-
0024350881
-
Cancer and the Peutz-Jeghers syndrome
-
Spigelman AD, Murday V, Phillips RK (1989) Cancer and the Peutz-Jeghers syndrome. Gut 30: 1588-1590
-
(1989)
Gut
, vol.30
, pp. 1588-1590
-
-
Spigelman, A.D.1
Murday, V.2
Phillips, R.K.3
-
26
-
-
14444280886
-
Carney Complex, Peutz-Jeghers Syndrome. Cowden Disease, and Bannayan-Zonana Syndrome share cutaneous and endocrine manifestation, but not genetic loci
-
Stratakis CA, Kirschner LS, Taymans SE, Tomlinson IPM, Marsh DJ, TOrpy DJ, Giatzakis C, Eccles DM, Theaker J, Houlston RS, Blouin J-L, Antonarakis SE, Basson CT, Eng C, Carney JA (1998) Carney Complex, Peutz-Jeghers Syndrome. Cowden Disease, and Bannayan-Zonana Syndrome share cutaneous and endocrine manifestation, but not genetic loci. J Clin End Met 8: 2972-2976
-
(1998)
J Clin End Met
, vol.8
, pp. 2972-2976
-
-
Stratakis, C.A.1
Kirschner, L.S.2
Taymans, S.E.3
Tomlinson, I.P.M.4
Marsh, D.J.5
TOrpy, D.J.6
Giatzakis, C.7
Eccles, D.M.8
Theaker, J.9
Houlston, R.S.10
Blouin, J.-L.11
Antonarakis, S.E.12
Basson, C.T.13
Eng, C.14
Carney, J.A.15
-
27
-
-
0033523268
-
Cancer risks in BRCA2 mutation carriers
-
The Breast Cancer Linkage Consortium (1999) Cancer risks in BRCA2 mutation carriers. JNCI 91: 1310-1316
-
(1999)
JNCI
, vol.91
, pp. 1310-1316
-
-
-
29
-
-
0023263472
-
Carcinoma and polyps of the gallbladder associated with Peutz-Jeghers syndrome
-
Wada K, Tanaka M, Yamaguchi K (1987) Carcinoma and polyps of the gallbladder associated with Peutz-Jeghers syndrome. Dig Dis Sci 32: 943-946
-
(1987)
Dig Dis Sci
, vol.32
, pp. 943-946
-
-
Wada, K.1
Tanaka, M.2
Yamaguchi, K.3
-
30
-
-
0032947283
-
Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients
-
Wang Z-J, Churchman M, Avizienyte E, McKeown C, Davies S, Evans DGR, Ferguson A, Ellis I, Xu W-H, Yan Z-Y, Aaltonen LA, Tomlinson IPM (1999) Germline mutations of the LKB1 (STK11) gene in Peutz-Jeghers patients. J Med Genet 36: 365-368
-
(1999)
J Med Genet
, vol.36
, pp. 365-368
-
-
Wang, Z.-J.1
Churchman, M.2
Avizienyte, E.3
McKeown, C.4
Davies, S.5
Evans, D.G.R.6
Ferguson, A.7
Ellis, I.8
Xu, W.-H.9
Yan, Z.-Y.10
Aaltonen, L.A.11
Tomlinson, I.P.M.12
-
31
-
-
0033012429
-
Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families
-
Westerman AM, Entius MM, Boor PPC, Koole R, de Baar E, Offerhaus GJA, Lubinski J, Lindhout D, Halley DJJ, de Rooij FWM, Wilson JHP (1999) Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families. Hum Mut 13: 476-481
-
(1999)
Hum Mut
, vol.13
, pp. 476-481
-
-
Westerman, A.M.1
Entius, M.M.2
Boor, P.P.C.3
Koole, R.4
De Baar, E.5
Offerhaus, G.J.A.6
Lubinski, J.7
Lindhout, D.8
Halley, D.J.J.9
De Rooij, F.W.M.10
Wilson, J.H.P.11
-
32
-
-
0032610848
-
Peutz-Jegher syndrome: Risks of a hereditary condition. A clinical review
-
Westerman AM, Wilson JHP (1999) Peutz-Jegher syndrome: risks of a hereditary condition. A clinical review. Scand J Gastro S230: 64-70
-
(1999)
Scand J Gastro
, vol.S230
, pp. 64-70
-
-
Westerman, A.M.1
Wilson, J.H.P.2
-
34
-
-
0035011886
-
Hamartomatous polyposis syndrome: Molecular genetics, neoplastic risk, and surveillance recommendations
-
Wirtzfeld DA, Petrelli NJ, Rodriguez-Bigas MA (2001) Hamartomatous polyposis syndrome: molecular genetics, neoplastic risk, and surveillance recommendations. Ann Surg Oncol ; 8: 319-327
-
(2001)
Ann Surg Oncol
, vol.8
, pp. 319-327
-
-
Wirtzfeld, D.A.1
Petrelli, N.J.2
Rodriguez-Bigas, M.A.3
-
35
-
-
0032906537
-
Mutations and impaired function of LKB1 in familial and non familial Peutz-Jeghers syndrome and a sporadic testicular cancer
-
Ylikorkala A, Avizienyte E, Tomlinson IPM, Tiainen M, Roth S, Loukola A, Hemminki A, Johansson M, Sistonen P, Markie D, Neale K, Phillips R, Zauber P, Twama T, Sampson J, Jarvinen H, Makela TP, Aaltonen LA (1999) Mutations and impaired function of LKB1 in familial and non familial Peutz-Jeghers syndrome and a sporadic testicular cancer. Hum Mol Genet 8: 45-51
-
(1999)
Hum Mol Genet
, vol.8
, pp. 45-51
-
-
Ylikorkala, A.1
Avizienyte, E.2
Tomlinson, I.P.M.3
Tiainen, M.4
Roth, S.5
Loukola, A.6
Hemminki, A.7
Johansson, M.8
Sistonen, P.9
Markie, D.10
Neale, K.11
Phillips, R.12
Zauber, P.13
Twama, T.14
Sampson, J.15
Jarvinen, H.16
Makela, T.P.17
Aaltonen, L.A.18
-
36
-
-
0034106282
-
Germline mutations of the gene in Korean Peutz-Jeghers syndrome patients
-
Yoon K-A, Ku J-L, Choi HS, Heo SC, Jeong S-Y, Park YJ, Kim NK, Kim JC, Jung PM, Park J-G (2000) Germline mutations of the gene in Korean Peutz-Jeghers syndrome patients. Br J Cancer 82: 1403-1406
-
(2000)
Br J Cancer
, vol.82
, pp. 1403-1406
-
-
Yoon, K.-A.1
Ku, J.-L.2
Choi, H.S.3
Heo, S.C.4
Jeong, S.-Y.5
Park, Y.J.6
Kim, N.K.7
Kim, J.C.8
Jung, P.M.9
Park, J.-G.10
-
37
-
-
0028888507
-
Feminizing Sertoli cell tumors in boys with Peutz-Jeghers syndrome
-
Young S, Gooneratne S, Straus II FH, Zeller WP, Bulun SE, Rosenthal IM (1995) Feminizing Sertoli cell tumors in boys with Peutz-Jeghers syndrome. Am J Surg Path 19: 50-58
-
(1995)
Am J Surg Path
, vol.19
, pp. 50-58
-
-
Young, S.1
Gooneratne, S.2
Straus F.H. II3
Zeller, W.P.4
Bulun, S.E.5
Rosenthal, I.M.6
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