-
1
-
-
0029150491
-
Desmoplastic fibroblastoma: A report of seven cases
-
Evans HL. Desmoplastic fibroblastoma: a report of seven cases. Am J Surg Pathol 1995;19:1077-81.
-
(1995)
Am J Surg Pathol
, vol.19
, pp. 1077-1081
-
-
Evans, H.L.1
-
3
-
-
0031837233
-
Collagenous fibroma (desmoplastic fibroblastoma): Report of four cases and review of the literature
-
Hasegawa T, Shimoda T, Hirohashi S, Hizawa K, Sano T. Collagenous fibroma (desmoplastic fibroblastoma): report of four cases and review of the literature. Arch Pathol Lab Med 1998;122:455-60.
-
(1998)
Arch Pathol Lab Med
, vol.122
, pp. 455-460
-
-
Hasegawa, T.1
Shimoda, T.2
Hirohashi, S.3
Hizawa, K.4
Sano, T.5
-
4
-
-
0031828337
-
Collagenous fibroma (desmoplastic fibroblastoma): A clinicopathologic analysis of 63 cases of a distinctive soft tissue lesion with stellate-shaped fibroblasts
-
Miettinen M, Fetsch JF. Collagenous fibroma (desmoplastic fibroblastoma): a clinicopathologic analysis of 63 cases of a distinctive soft tissue lesion with stellate-shaped fibroblasts. Hum Pathol 1998;29:676-82.
-
(1998)
Hum Pathol
, vol.29
, pp. 676-682
-
-
Miettinen, M.1
Fetsch, J.F.2
-
6
-
-
0030455755
-
Trisomies 8 and 20 in desmoid tumors
-
Qi H, Dal Cin P, Hernandez JM, Garcia JL, Sciot R, Fletcher C, et al. Trisomies 8 and 20 in desmoid tumors. Cancer Genet Cytogenet 1996;92:147-9.
-
(1996)
Cancer Genet Cytogenet
, vol.92
, pp. 147-149
-
-
Qi, H.1
Dal Cin, P.2
Hernandez, J.M.3
Garcia, J.L.4
Sciot, R.5
Fletcher, C.6
-
7
-
-
0030332895
-
Deletion 5q in desmoid tumor and fluorescence in situ hybridization for chromosome 8 and/or 20 copy number
-
Bridge JA, Meloni AA, Neff JR, Deboer J, Pickering D, Dalence C, et al. Deletion 5q in desmoid tumor and fluorescence in situ hybridization for chromosome 8 and/or 20 copy number. Cancer Genet Cytogenet 1996;92:150-1.
-
(1996)
Cancer Genet Cytogenet
, vol.92
, pp. 150-151
-
-
Bridge, J.A.1
Meloni, A.A.2
Neff, J.R.3
Deboer, J.4
Pickering, D.5
Dalence, C.6
-
9
-
-
0032189996
-
Involvement of 3q21 in nodular fasciitis: Possibly a new nonrandomly associated anomaly
-
Wiebolt VM, Roberts CA, Suijkerbuijk RF, Pickering D, Neff JR, Bridge JA. Involvement of 3q21 in nodular fasciitis: possibly a new nonrandomly associated anomaly. Cancer Genet Cytogenet 1998;106:177-9.
-
(1998)
Cancer Genet Cytogenet
, vol.106
, pp. 177-179
-
-
Wiebolt, V.M.1
Roberts, C.A.2
Suijkerbuijk, R.F.3
Pickering, D.4
Neff, J.R.5
Bridge, J.A.6
-
10
-
-
0029114049
-
Cytogenetic findings in a case of nodular fasciitis of the breast
-
Birdsall SH, Shipley JM, Summersgill BM, Black AJM, Jackson P, Kissin MW, et al. Cytogenetic findings in a case of nodular fasciitis of the breast. Cancer Genet Cytogenet 1995; 81:166-8.
-
(1995)
Cancer Genet Cytogenet
, vol.81
, pp. 166-168
-
-
Birdsall, S.H.1
Shipley, J.M.2
Summersgill, B.M.3
Black, A.J.M.4
Jackson, P.5
Kissin, M.W.6
-
11
-
-
0343267791
-
Trisomy 21 in solitary fibrous tumor
-
Dal Cin P, Sciot R, Fletcher CDM, Hilliker C, de Wever I, van Damme B, et al. Trisomy 21 in solitary fibrous tumor. Cancer Genet Cytogenet 1996;86:58-60.
-
(1996)
Cancer Genet Cytogenet
, vol.86
, pp. 58-60
-
-
Dal Cin, P.1
Sciot, R.2
Fletcher, C.D.M.3
Hilliker, C.4
De Wever, I.5
Van Damme, B.6
-
12
-
-
0018629324
-
Fibroma of tendon sheath
-
Chung EB, Enzinger F. Fibroma of tendon sheath. Cancer 1979;44:1945-54.
-
(1979)
Cancer
, vol.44
, pp. 1945-1954
-
-
Chung, E.B.1
Enzinger, F.2
-
13
-
-
0345494321
-
Tumors of neural origin
-
Sandberg AA, Bridge JA, editors. Austin, TX: R.G. Landes
-
Sandberg AA, Bridge JA. Tumors of neural origin. In: Sandberg AA, Bridge JA, editors. The cytogenetics of bone and soft tissue tumors. Austin, TX: R.G. Landes; 1994. p. 229-312.
-
(1994)
The Cytogenetics of Bone and Soft Tissue Tumors
, pp. 229-312
-
-
Sandberg, A.A.1
Bridge, J.A.2
-
14
-
-
0028909493
-
Deletion mapping of the long arm of chromosome 22 in human meningiomas
-
Akagi K, Kurahashi H, Arita N, Hayakawa T, Monden M, Mori T, et al. Deletion mapping of the long arm of chromosome 22 in human meningiomas. Int J Cancer 1995;60:178-82.
-
(1995)
Int J Cancer
, vol.60
, pp. 178-182
-
-
Akagi, K.1
Kurahashi, H.2
Arita, N.3
Hayakawa, T.4
Monden, M.5
Mori, T.6
-
15
-
-
0028276445
-
Deletions on chromosome 22 in sporadic meningioma
-
Ruttledge MH, Xie YG, Han FY, Peyrard M, Collins VP, Nordenskjöld M, et al. Deletions on chromosome 22 in sporadic meningioma. Genes Chromosom Cancer 1994;10:122-30.
-
(1994)
Genes Chromosom Cancer
, vol.10
, pp. 122-130
-
-
Ruttledge, M.H.1
Xie, Y.G.2
Han, F.Y.3
Peyrard, M.4
Collins, V.P.5
Nordenskjöld, M.6
-
16
-
-
0031051644
-
Soft tissue perineurioma: Evidence for an abnormality of chromosome 22, criteria for diagnosis, and review of the literature
-
Giannini C, Scheithauer BW, Jenkins RB, Erlandson RA, Perry A, Borell TJ, et al. Soft tissue perineurioma: evidence for an abnormality of chromosome 22, criteria for diagnosis, and review of the literature. Am J Surg Pathol 1997;21:164-73.
-
(1997)
Am J Surg Pathol
, vol.21
, pp. 164-173
-
-
Giannini, C.1
Scheithauer, B.W.2
Jenkins, R.B.3
Erlandson, R.A.4
Perry, A.5
Borell, T.J.6
-
17
-
-
0344655666
-
Cutaneous sclerosing perineurioma with cryptic NF2 gene deletion
-
in press
-
Sciot R, Dal Cin P, Hagemeijer A, de Smet L, van Damme B, van den Berghe H. Cutaneous sclerosing perineurioma with cryptic NF2 gene deletion. Am J Surg Pathol 1999 (in press).
-
(1999)
Am J Surg Pathol
-
-
Sciot, R.1
Dal Cin, P.2
Hagemeijer, A.3
De Smet, L.4
Van Damme, B.5
Van Den Berghe, H.6
-
18
-
-
0028792196
-
Monosomy 22 in a malignant peripheral nerve sheath tumor of the kidney in childhood: A genetic link with other malignant pediatric renal neoplasms?
-
Sciot R, Dal Cin P, Fletcher C, de Wever I, de Vos R, van Damme B, et al. Monosomy 22 in a malignant peripheral nerve sheath tumor of the kidney in childhood: a genetic link with other malignant pediatric renal neoplasms? Histopathology 1995;27:373-6.
-
(1995)
Histopathology
, vol.27
, pp. 373-376
-
-
Sciot, R.1
Dal Cin, P.2
Fletcher, C.3
De Wever, I.4
De Vos, R.5
Van Damme, B.6
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