-
1
-
-
0029133473
-
Intracranial ependymomas of childhood: Long-term outcome and prognostic factors
-
Pollack IF, Gerszten PC, Martinez AJ, Lo KH, Shultz B, Albright AL, Janosky J, Deutsch M: Intracranial ependymomas of childhood: long-term outcome and prognostic factors. Neurosurgery 37: 655-667, 1995
-
(1995)
Neurosurgery
, vol.37
, pp. 655-667
-
-
Pollack, I.F.1
Gerszten, P.C.2
Martinez, A.J.3
Lo, K.H.4
Shultz, B.5
Albright, A.L.6
Janosky, J.7
Deutsch, M.8
-
2
-
-
0025657060
-
Prognostic factors in childhood ependymomas
-
Sutton LN, Goldwein J, Perilongo G, Lange BJ, Schut L, Rorke LB, Packer R: Prognostic factors in childhood ependymomas. Pediatr Neurosurg 16: 57-65, 1991
-
(1991)
Pediatr Neurosurg
, vol.16
, pp. 57-65
-
-
Sutton, L.N.1
Goldwein, J.2
Perilongo, G.3
Lange, B.J.4
Schut, L.5
Rorke, L.B.6
Packer, R.7
-
3
-
-
0022506980
-
A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma
-
Friend SH, Bernards R, Rogelj S, Weinberg RA, Rapaport JM, Albert DM, Dryja TP: A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma. Nature 323: 643-646, 1986
-
(1986)
Nature
, vol.323
, pp. 643-646
-
-
Friend, S.H.1
Bernards, R.2
Rogelj, S.3
Weinberg, R.A.4
Rapaport, J.M.5
Albert, D.M.6
Dryja, T.P.7
-
4
-
-
0021327569
-
Loss of alleles at loci on human chromosome 11 during genesis of Wilm's tumor
-
Koufos A, Hansen MF, Lampkin BC, Workman ML, Copeland NG, Jenkins NA, Cavenee WK: Loss of alleles at loci on human chromosome 11 during genesis of Wilm's tumor. Nature 309: 170-172, 1984
-
(1984)
Nature
, vol.309
, pp. 170-172
-
-
Koufos, A.1
Hansen, M.F.2
Lampkin, B.C.3
Workman, M.L.4
Copeland, N.G.5
Jenkins, N.A.6
Cavenee, W.K.7
-
5
-
-
0027438827
-
Combinatorial generation of variable fusion proteins in the Ewing family of tumors
-
Zucman J, Melot T, Desmaze C, Ghysdael J, Plougastel B, Peter M, Zucker JM, Triche TJ, Sheer D, Turc-Carel C: Combinatorial generation of variable fusion proteins in the Ewing family of tumors. EMBO J 12: 4481-4487, 1993
-
(1993)
EMBO J
, vol.12
, pp. 4481-4487
-
-
Zucman, J.1
Melot, T.2
Desmaze, C.3
Ghysdael, J.4
Plougastel, B.5
Peter, M.6
Zucker, J.M.7
Triche, T.J.8
Sheer, D.9
Turc-Carel, C.10
-
6
-
-
0027534945
-
Rearrangement of the PAX 3 paired box gene in the pediatric solid tumour alveolar rhabdomyosarcoma
-
Barr FG, Galili N, Holick J, Biegel JA, Rovera G, Emanuel BS: Rearrangement of the PAX 3 paired box gene in the pediatric solid tumour alveolar rhabdomyosarcoma. Nature Genet 3: 113-117, 1993
-
(1993)
Nature Genet
, vol.3
, pp. 113-117
-
-
Barr, F.G.1
Galili, N.2
Holick, J.3
Biegel, J.A.4
Rovera, G.5
Emanuel, B.S.6
-
7
-
-
0026676710
-
Cytogenetic and loss of heterozygosity studies in ependymomas, pilocytic astrocytomas, and oligodendrogliomas
-
Ransom DT, Ritland SR, Kimmel DW, Moertel CA, Dahl RJ, Scheithauer BW, Kelly PJ, Jenkins RB : Cytogenetic and loss of heterozygosity studies in ependymomas, pilocytic astrocytomas, and oligodendrogliomas. Genes Chrom Cancer 5: 348-356, 1992
-
(1992)
Genes Chrom Cancer
, vol.5
, pp. 348-356
-
-
Ransom, D.T.1
Ritland, S.R.2
Kimmel, D.W.3
Moertel, C.A.4
Dahl, R.J.5
Scheithauer, B.W.6
Kelly, P.J.7
Jenkins, R.B.8
-
8
-
-
0024462515
-
Cytogenetic abnormalities in human ependymomas
-
Stratton MD, Darling J, Lantos PL, Cooper CS, Reeves BR: Cytogenetic abnormalities in human ependymomas. Int J Cancer 44: 579-581, 1989
-
(1989)
Int J Cancer
, vol.44
, pp. 579-581
-
-
Stratton, M.D.1
Darling, J.2
Lantos, P.L.3
Cooper, C.S.4
Reeves, B.R.5
-
9
-
-
0025143557
-
Loss of genetic information in central nervous system tumors common to children and young adults
-
James CD, He J, Carlbom E, Mikkelsen T, Ridderheim PA, Cavenee WK, Collins VP: Loss of genetic information in central nervous system tumors common to children and young adults. Genes Chrom Cancer 2: 94-102, 1990
-
(1990)
Genes Chrom Cancer
, vol.2
, pp. 94-102
-
-
James, C.D.1
He, J.2
Carlbom, E.3
Mikkelsen, T.4
Ridderheim, P.A.5
Cavenee, W.K.6
Collins, V.P.7
-
11
-
-
0026694294
-
Chromosome abnormalities in low-grade central nervous system tumors
-
Griffin CA, LongPP, Carson BS, Brem H: Chromosome abnormalities in low-grade central nervous system tumors. Cancer Genet Cytogenet 60: 67-73, 1992
-
(1992)
Cancer Genet Cytogenet
, vol.60
, pp. 67-73
-
-
Griffin, C.A.1
Long, P.P.2
Carson, B.S.3
Brem, H.4
-
12
-
-
0026544721
-
Karyotypes in 90 human gliomas
-
Thiel G, Losanowa T, Kintzel D, Nisch G, Martin H, Vorpahl K, Witkowski R: Karyotypes in 90 human gliomas. Cancer Genet Cytogenet 58: 109-120, 1992
-
(1992)
Cancer Genet Cytogenet
, vol.58
, pp. 109-120
-
-
Thiel, G.1
Losanowa, T.2
Kintzel, D.3
Nisch, G.4
Martin, H.5
Vorpahl, K.6
Witkowski, R.7
-
13
-
-
0026689599
-
Cytogenetic evidence for a chromosome 22 tumor suppressor gene in ependymoma
-
Weremowicz SK, Kupsky WJ, Morton CC, Fletcher JA: Cytogenetic evidence for a chromosome 22 tumor suppressor gene in ependymoma. Cancer Genet Cytogenet 61: 193-196, 1992
-
(1992)
Cancer Genet Cytogenet
, vol.61
, pp. 193-196
-
-
Weremowicz, S.K.1
Kupsky, W.J.2
Morton, C.C.3
Fletcher, J.A.4
-
14
-
-
0027489653
-
Chromosomes in the genesis and progression of ependymomas
-
Rogatto SR, Casartelli C, Rainho CA, Barbieri-Neto J: Chromosomes in the genesis and progression of ependymomas. Cancer Genet Cytogenet 69: 146-152, 1993
-
(1993)
Cancer Genet Cytogenet
, vol.69
, pp. 146-152
-
-
Rogatto, S.R.1
Casartelli, C.2
Rainho, C.A.3
Barbieri-Neto, J.4
-
15
-
-
0027405720
-
A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor
-
Trofatter JA, MacCollin MM, Rutter JL, Murrell JR, Duyao MP, Parry DM, Eldridge R, Kley N, Menon AG, Pulaski K, Haase VH, Ambrose CM, Munroe D, Bove C, Haines JL, Martuza RL, MacDonald ME, Seizinger BR, Short MP, Buckler AJ, Gusella JF: A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor. Cell 72: 791-800, 1993
-
(1993)
Cell
, vol.72
, pp. 791-800
-
-
Trofatter, J.A.1
MacCollin, M.M.2
Rutter, J.L.3
Murrell, J.R.4
Duyao, M.P.5
Parry, D.M.6
Eldridge, R.7
Kley, N.8
Menon, A.G.9
Pulaski, K.10
Haase, V.H.11
Ambrose, C.M.12
Munroe, D.13
Bove, C.14
Haines, J.L.15
Martuza, R.L.16
MacDonald, M.E.17
Seizinger, B.R.18
Short, M.P.19
Buckler, A.J.20
Gusella, J.F.21
more..
-
16
-
-
0028091283
-
The neurofibromatosis type 2 gene is inactivated in schwannomas
-
Twist EC, Ruttledge MH, Rousseau M, Sanson M, Papi L, Merel P, Delattre O, Rouleau GA: The neurofibromatosis type 2 gene is inactivated in schwannomas. Hum Mol Genet 3: 147-151, 1994
-
(1994)
Hum Mol Genet
, vol.3
, pp. 147-151
-
-
Twist, E.C.1
Ruttledge, M.H.2
Rousseau, M.3
Sanson, M.4
Papi, L.5
Merel, P.6
Delattre, O.7
Rouleau, G.A.8
-
17
-
-
0028264119
-
Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas
-
Ruttledge MH, Sarrazin J, Rangaratnam S, Phelan CM, Twist E, Merel P, Delattre O, Thomas G, Nordenskjöld M, Collins VP, Dumanski JP, Rouleau GA: Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas. Nature Gen 6: 180-184, 1994
-
(1994)
Nature Gen
, vol.6
, pp. 180-184
-
-
Ruttledge, M.H.1
Sarrazin, J.2
Rangaratnam, S.3
Phelan, C.M.4
Twist, E.5
Merel, P.6
Delattre, O.7
Thomas, G.8
Nordenskjöld, M.9
Collins, V.P.10
Dumanski, J.P.11
Rouleau, G.A.12
-
18
-
-
0029004033
-
Predomiant occurrence of somatic mutations of the NF2 gene in meningiomas and schwannomas
-
Merel P, Hoang-Xuan K, Sanson M, Moreau-Aubry A, Bijlsma EK, Lazaro C, Moisan JP, Resche F, Nishisho I, Estivill X, Delattre JY, Poisson M, Theillet C, Hulsebos T, Delattre O, Thomas G: Predomiant occurrence of somatic mutations of the NF2 gene in meningiomas and schwannomas. Genes Chrom Cancer 13: 211-216, 1995
-
(1995)
Genes Chrom Cancer
, vol.13
, pp. 211-216
-
-
Merel, P.1
Hoang-Xuan, K.2
Sanson, M.3
Moreau-Aubry, A.4
Bijlsma, E.K.5
Lazaro, C.6
Moisan, J.P.7
Resche, F.8
Nishisho, I.9
Estivill, X.10
Delattre, J.Y.11
Poisson, M.12
Theillet, C.13
Hulsebos, T.14
Delattre, O.15
Thomas, G.16
-
20
-
-
0029123934
-
Exon scanning for mutations of the NF2 gene in pediatric ependymomas, rhabdoid tumors and meningiomas
-
Slave I, MacCollin MM, Dunn M, Jones S, Sutton LN, Gusella JF, Biegel JA: Exon scanning for mutations of the NF2 gene in pediatric ependymomas, rhabdoid tumors and meningiomas. Int J Cancer 64: 243-247, 1995
-
(1995)
Int J Cancer
, vol.64
, pp. 243-247
-
-
Slave, I.1
MacCollin, M.M.2
Dunn, M.3
Jones, S.4
Sutton, L.N.5
Gusella, J.F.6
Biegel, J.A.7
-
21
-
-
0029820302
-
Molecular genetic analysis of chromosome arm 17p and chromosome arm 22q DNA sequences in sporadic pediatric ependymomas
-
von Haken MS, White EC, Daneshvar-Shyesther L, Sih S, Choi E, Kalra R, Cogen PH: Molecular genetic analysis of chromosome arm 17p and chromosome arm 22q DNA sequences in sporadic pediatric ependymomas. Genes Chrom Cancer 17: 37-44, 1996
-
(1996)
Genes Chrom Cancer
, vol.17
, pp. 37-44
-
-
Von Haken, M.S.1
White, E.C.2
Daneshvar-Shyesther, L.3
Sih, S.4
Choi, E.5
Kalra, R.6
Cogen, P.H.7
-
22
-
-
0029129297
-
Molecular analysis of genetic changes in ependymomas
-
Bijlsma EK, Voesten AMJ, Bijleveld EH, Troost D, Westerveld A, Merel P, Thomas G, Hulsebos TJM: Molecular analysis of genetic changes in ependymomas. Genes Chrom Cancer 13: 272-277, 1995
-
(1995)
Genes Chrom Cancer
, vol.13
, pp. 272-277
-
-
Bijlsma, E.K.1
Voesten, A.M.J.2
Bijleveld, E.H.3
Troost, D.4
Westerveld, A.5
Merel, P.6
Thomas, G.7
Hulsebos, T.J.M.8
-
23
-
-
0026347639
-
p53 mutations in nonastrocytic human brain tumors
-
Ohgaki H, Eibl RH, Wiestler OD, Yasargil MG, Newcomb EW, Kleihues P: p53 mutations in nonastrocytic human brain tumors. Cancer Res 51: 6202-6205, 1991
-
(1991)
Cancer Res
, vol.51
, pp. 6202-6205
-
-
Ohgaki, H.1
Eibl, R.H.2
Wiestler, O.D.3
Yasargil, M.G.4
Newcomb, E.W.5
Kleihues, P.6
-
24
-
-
0025868284
-
Identification of a germ-line mutation in the p53 gene in a patient with an intracranial ependymoma
-
Metzger AK, Sheffield VC, Duyk G, Daneshvar L, Edwards MSB, Cogen PH: Identification of a germ-line mutation in the p53 gene in a patient with an intracranial ependymoma. Proc Natl Acad Sci USA 88: 7825-7829, 1991
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 7825-7829
-
-
Metzger, A.K.1
Sheffield, V.C.2
Duyk, G.3
Daneshvar, L.4
Edwards, M.S.B.5
Cogen, P.H.6
-
25
-
-
0028881850
-
p53 gene mutations in pediatric brain tumors
-
Felix CA, Slave I, Dunn M, Strauss EA, Phillips PC, Rorke LB, Sutton LN, Bunin GR, Biegel JA : p53 gene mutations in pediatric brain tumors. Med Pediatr Oncol 25: 431-436, 1995
-
(1995)
Med Pediatr Oncol
, vol.25
, pp. 431-436
-
-
Felix, C.A.1
Slave, I.2
Dunn, M.3
Strauss, E.A.4
Phillips, P.C.5
Rorke, L.B.6
Sutton, L.N.7
Bunin, G.R.8
Biegel, J.A.9
-
26
-
-
0030054135
-
Infrequency of p53 gene mutations in ependymomas
-
Fink KL, Rushing EJ, Schold Jr SC, Nisen PD : Infrequency of p53 gene mutations in ependymomas. J Neuro-Oncol 27: 111-115, 1996
-
(1996)
J Neuro-Oncol
, vol.27
, pp. 111-115
-
-
Fink, K.L.1
Rushing, E.J.2
Schold Jr., S.C.3
Nisen, P.D.4
-
27
-
-
0026513426
-
Involvement of multiple chromosome 17p loci in medulloblastoma tumorigenesis
-
Cogen PH, Daneshvar L, Metzger AK, Duyk G, Edwards MSB, Sheffield VC: Involvement of multiple chromosome 17p loci in medulloblastoma tumorigenesis. Am J Hum Genet 50: 584-589, 1992
-
(1992)
Am J Hum Genet
, vol.50
, pp. 584-589
-
-
Cogen, P.H.1
Daneshvar, L.2
Metzger, A.K.3
Duyk, G.4
Edwards, M.S.B.5
Sheffield, V.C.6
-
28
-
-
0026634161
-
Evidence for a 17p tumor related locus distinct from p53 in pediatric primitive neuroectodermal tumors
-
Biegel JA, Burk CD, Barr FG, Emanuel BS: Evidence for a 17p tumor related locus distinct from p53 in pediatric primitive neuroectodermal tumors. Cancer Res 52: 3391-3395, 1992
-
(1992)
Cancer Res
, vol.52
, pp. 3391-3395
-
-
Biegel, J.A.1
Burk, C.D.2
Barr, F.G.3
Emanuel, B.S.4
-
29
-
-
0027290895
-
Absence of p53 mutations in childhood central nervous system primitive neuroectodermal tumors
-
Raffel CT, Thomas GA, Tishler DM, Lassoff S, Allen JC: Absence of p53 mutations in childhood central nervous system primitive neuroectodermal tumors. Neurosurgery 33: 301-306, 1993
-
(1993)
Neurosurgery
, vol.33
, pp. 301-306
-
-
Raffel, C.T.1
Thomas, G.A.2
Tishler, D.M.3
Lassoff, S.4
Allen, J.C.5
-
31
-
-
0029153985
-
Isochromosome 17q demonstrated by interphase fluorescence in situ hybridization in primitive neuroectodermal tumors of the central nervous system
-
Biegel JA, Rorke LB, Janss AJ, Sutton LN, Parmiter AH: Isochromosome 17q demonstrated by interphase fluorescence in situ hybridization in primitive neuroectodermal tumors of the central nervous system. Genes Chrom Cancer 14: 85-96, 1995
-
(1995)
Genes Chrom Cancer
, vol.14
, pp. 85-96
-
-
Biegel, J.A.1
Rorke, L.B.2
Janss, A.J.3
Sutton, L.N.4
Parmiter, A.H.5
-
32
-
-
0002345846
-
-
Davis KE, Tilghman SM (eds) Cold Spring Harbor NY: Cold Spring Harbor Laboratory Press
-
Lehrach H et al.: In: Davis KE, Tilghman SM (eds) Genome Analysis Volume I: Genetic and Physical Mapping. Cold Spring Harbor NY: Cold Spring Harbor Laboratory Press 39-81, 1990
-
(1990)
Genome Analysis Volume I: Genetic and Physical Mapping
, vol.1
, pp. 39-81
-
-
Lehrach, H.1
-
33
-
-
0029682255
-
Narrowing the critical region for a rhabdoid tumor locus in 22q11
-
Biegel JA, Allen CS, Kawasaki K, Shimizu N, Budarf ML, Bell CJ: Narrowing the critical region for a rhabdoid tumor locus in 22q11. Genes Chrom Cancer 16: 94-105, 1996
-
(1996)
Genes Chrom Cancer
, vol.16
, pp. 94-105
-
-
Biegel, J.A.1
Allen, C.S.2
Kawasaki, K.3
Shimizu, N.4
Budarf, M.L.5
Bell, C.J.6
-
34
-
-
0029984281
-
Allele loss on chromosome arm 6q and fine mapping of the region at 6q27 in epithelial ovarian cancer
-
Cooke IE, Shelling AN, Le Meuth VG, Charnock ML, Ganesan TS: Allele loss on chromosome arm 6q and fine mapping of the region at 6q27 in epithelial ovarian cancer. Genes Chrom Cancer 15: 223-233, 1996
-
(1996)
Genes Chrom Cancer
, vol.15
, pp. 223-233
-
-
Cooke, I.E.1
Shelling, A.N.2
Le Meuth, V.G.3
Charnock, M.L.4
Ganesan, T.S.5
-
35
-
-
0028891541
-
A strategy for constructing high-resolution genetic maps of the human genome: A genetic map of chromosome 17p, ordered with meiotic breakpoint-mapping panels
-
Gerken SC, Albertsen H, Eisner T, Ballard L, Holik P, Lawrence E, Moore M, Zhao X, White R: A strategy for constructing high-resolution genetic maps of the human genome: A genetic map of chromosome 17p, ordered with meiotic breakpoint-mapping panels. Am J Hum Genet 56: 484-499, 1995
-
(1995)
Am J Hum Genet
, vol.56
, pp. 484-499
-
-
Gerken, S.C.1
Albertsen, H.2
Eisner, T.3
Ballard, L.4
Holik, P.5
Lawrence, E.6
Moore, M.7
Zhao, X.8
White, R.9
-
36
-
-
0027501055
-
A microsatellitebased multipoint index map of human chromosome 22
-
Buetow KH, Duggan D, Yang B, Ludwigsen S, Puck J, Porter J, Budarf M, Spielman R, Emanuel BS: A microsatellitebased multipoint index map of human chromosome 22. Genomics 18: 329-339, 1993
-
(1993)
Genomics
, vol.18
, pp. 329-339
-
-
Buetow, K.H.1
Duggan, D.2
Yang, B.3
Ludwigsen, S.4
Puck, J.5
Porter, J.6
Budarf, M.7
Spielman, R.8
Emanuel, B.S.9
-
37
-
-
0027739843
-
Cytogenetic analysis of 109 pediatric central nervous system tumors
-
Neumann E, Kalousek DK, Norman MG, Steinbok P, Cochrane DD, Goddard K: Cytogenetic analysis of 109 pediatric central nervous system tumors. Cancer Genet Cytogenet 71: 40-49, 1993
-
(1993)
Cancer Genet Cytogenet
, vol.71
, pp. 40-49
-
-
Neumann, E.1
Kalousek, D.K.2
Norman, M.G.3
Steinbok, P.4
Cochrane, D.D.5
Goddard, K.6
-
38
-
-
0028348219
-
Evidence of allelic imbalance of chromosome 6 in human astrocytomas
-
Liang BC, Ross DA, Greenberg HS, Meltzer PS, Trent JM: Evidence of allelic imbalance of chromosome 6 in human astrocytomas. Neurology 44: 533-536, 1994
-
(1994)
Neurology
, vol.44
, pp. 533-536
-
-
Liang, B.C.1
Ross, D.A.2
Greenberg, H.S.3
Meltzer, P.S.4
Trent, J.M.5
-
39
-
-
0023750335
-
Fragile X Syndrome and Neoplasia
-
Phelan MC, Stevenson RE, Collins JL, Trent HE: Fragile X Syndrome and Neoplasia. Am J Med Genet 30: 77-82, 1988
-
(1988)
Am J Med Genet
, vol.30
, pp. 77-82
-
-
Phelan, M.C.1
Stevenson, R.E.2
Collins, J.L.3
Trent, H.E.4
-
40
-
-
0020607289
-
Demonstration of the fra(X) in lymphocytes, fibroblasts, and bone marrow in a patient with a testicular tumor
-
del Pozo BC, Millard PR: Demonstration of the fra(X) in lymphocytes, fibroblasts, and bone marrow in a patient with a testicular tumor. J Med Genet 20: 225-227, 1983
-
(1983)
J Med Genet
, vol.20
, pp. 225-227
-
-
Del Pozo, B.C.1
Millard, P.R.2
-
41
-
-
0023232926
-
Central nervous system neoplasm in a young man with Martin-Bell syndrome -fra(X)-XLMR
-
Rodewald L, Miller DC, Sciorra L, Barabas G, Lee M: Central nervous system neoplasm in a young man with Martin-Bell syndrome -fra(X)-XLMR. Am J Med Genet 26: 7-12, 1987
-
(1987)
Am J Med Genet
, vol.26
, pp. 7-12
-
-
Rodewald, L.1
Miller, D.C.2
Sciorra, L.3
Barabas, G.4
Lee, M.5
-
42
-
-
0022259183
-
On the meaning of fragile sites in cancer risk and development
-
Shabtai F, Klar D, Hart J, Halbrecht I: On the meaning of fragile sites in cancer risk and development. Cancer Genet Cytogenet 18: 81-85, 1985
-
(1985)
Cancer Genet Cytogenet
, vol.18
, pp. 81-85
-
-
Shabtai, F.1
Klar, D.2
Hart, J.3
Halbrecht, I.4
-
43
-
-
0028240051
-
Chromosomal aberrations in four ependymomas
-
Sawyer JR, Sammartino G, Husain M, Boop FA, Chadduck WM: Chromosomal aberrations in four ependymomas. Cancer Genet Cytogenet 74: 132-138, 1994
-
(1994)
Cancer Genet Cytogenet
, vol.74
, pp. 132-138
-
-
Sawyer, J.R.1
Sammartino, G.2
Husain, M.3
Boop, F.A.4
Chadduck, W.M.5
|