Access the full text.
Sign up today, get DeepDyve free for 14 days.
Juan Rey, M. Bello, J. Campos, Jesús Vaquero, M. Kusak, J. Sarasa, A. Pestaña (1993)
Abnormalities of chromosome 22 in human brain tumors determined by combined cytogenetic and molecular genetic approaches.Cancer genetics and cytogenetics, 66 1
J. Trent, J. Casper, P. Meltzer, F. Thompson, J. Fogh (1985)
Nonrandom chromosome alterations in rhabdomyosarcoma.Cancer genetics and cytogenetics, 16 3
M. Tucker, G. D'angio, J. Boice, L. Strong, Frederick Li, M. Stovall, B. Stone, D. Green, F. Lombardi, William Newton, R. Hoover, J. Fraumeni (1987)
Bone sarcomas linked to radiotherapy and chemotherapy in children.The New England journal of medicine, 317 10
(1991)
Guidelines for Cancer Cytogenetics, Supplement to An International System for Human Cytogenetic Nomenclature. Mitelman F (ed)
V. Riccardi, D. Elder (1986)
Multiple cytogenetic aberrations in neurofibrosarcomas complicating neurofibromatosis.Cancer genetics and cytogenetics, 23 3
J. Mark, C. Ekedahl (1987)
Polyclonal chromosomal evolution in a benign mixed salivary gland tumor.Cancer genetics and cytogenetics, 28 2
Jacqueline Whang-Peng, T. Triche, Turid Knutsen, J. Miser, Edwin Douglass, Mark Israel (1984)
Chromosome translocation in peripheral neuroepithelioma.The New England journal of medicine, 311 9
B. Seizinger, G. Rouleau, L. Ozelius, A. Lane, P. George-hyslop, S. Huson, J. Gusella, R. Martuza (1987)
Common pathogenetic mechanism for three tumor types in bilateral acoustic neurofibromatosis.Science, 236 4799
A. Gown (1978)
Multicellular origin of parathyroid "adenomas".The New England journal of medicine, 298 1
T. Glover (1992)
Catalog of chromosome aberrations in cancer, 4th edAmerican Journal of Human Genetics, 50
J. Fountain, M. Wallace, Anne Brereton, P. O'Connell, White Rl, Rich Dc, Ledbetter Dh, R. Leach, Fournier Re, A. Menon (1989)
Physical mapping of the von Recklinghausen neurofibromatosis region on chromosome 17.American journal of human genetics, 44 1
E. Bijlsma, R. Brouwer-Mladin, D. Bosch, A. Westerveld, T. Hulsebos (1992)
Molecular characterization of chromosome 22 deletions in schwannomasGenes, 5
V. Potluri, F. Gilbert (1985)
A cytogenetic study of embryonal rhabdomyosarcoma.Cancer genetics and cytogenetics, 14 1-2
isrics of classical and cellular schwannomas
J. Rey, M. Bello, M. Kusak, J. Campos, A. Pestaña (1993)
Involvement of 22q12 in a neurofibrosarcoma in neurofibromatosis type 1.Cancer genetics and cytogenetics, 66 1
Third International Workshop on Chromosomes in Solid Tumors (1989) The Arizona Cancer Center
D. Barker, E. Wright, K. Nguyen, L. Cannon, P. Fain, D. Goldgar, D. Bishop, J. Carey, B. Baty, J. Kivlin, H. Willard, J. Waye, G. Greig, L. Leinwand, Y. Nakamura, P. O'Connell, M. Leppert, J. Lalouel, Raymond White, M. Skolnick (1987)
Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17.Science, 236 4805
D. Rowe, M. Gerrard, B. Gibbons, J. Malpas (1987)
Two further cases of t(2;13) in alveolar rhabdomyosarcoma indicating a review of the published chromosome breakpoints.British Journal of Cancer, 56
Yuesheng Jin, S. Heim, N. Mandahl, A. Biörklund, J. Wennerberg, F. Mitelman (1990)
Multiple clonal chromosome aberrations in squamous cell carcinomas of the larynx.Cancer genetics and cytogenetics, 44 2
B. Seizinger, R. Martuza, J. Gusella (1986)
Loss of genes on chromosome 22 in tumorigenesis of human acoustic neuromaNature, 322
J. Woodruff, N. Chernik, Myron Smith, William Millett, F. Foote (1973)
Peripheral nerve tumors with rhabdomyosarcomatous differentiation (malignant “triton” tumors)Cancer, 32
J. Whang‐Peng, T. Knutsen, K. Theil, M. Horowitz, T. Triche (1992)
Cytogenetic studies in subgroups of rhabdomyosarcomaGenes, 5
P. O'Connell, R. Leach, R. Cawthon, M. Culver, J. Stevens, D. Viskochil, R. Fournier, D. Rich, D. Ledbetter, R. White (1989)
Two NF1 translocations map within a 600-kilobase segment of 17q11.2.Science, 244 4908
Christine Stephenson, Julia Bridge, Avery Sandberg (1992)
Cytogenetic and pathologic aspects of Ewing's sarcoma and neuroectodermal tumors.Human pathology, 23 11
C. Fletcher (1998)
Soft Tissue TumorsThe Journal of pathology, 159 4
R. Wolff, K. Frazer, R. Jackler, M. Lanser, L. Pitts, D. Cox (1992)
Analysis of chromosome 22 deletions in neurofibromatosis type 2-related tumors.American journal of human genetics, 51 3
M. Tucker, C. Coleman, R. Cox, A. Varghese, S. Rosenberg (1988)
Risk of second cancers after treatment for Hodgkin's disease.The New England journal of medicine, 318 2
J. Lai, J. Savary, M. Deminatti, M. Demaille, M. Baranzelli (1987)
Translocation (2;13)(q37;q14) in rhabdomyosarcoma: a new case.Cancer genetics and cytogenetics, 25 2
Wang Sheng, S. Soukup, E. Ballard, Betsy Gotwals, B. Lampkin (1988)
Chromosomal analysis of sixteen human rhabdomyosarcomas.Cancer research, 48 4
A. Garvin, W. Stanley, D. Bennett, J. Sullivan, D. Sens (1986)
The in vitro growth, heterotransplantation, and differentiation of a human rhabdomyosarcoma cell line.The American journal of pathology, 125 1
J. Whang‐Peng, C. Freter, T. Knutsen, J. Nanfro, A. Gazdar (1987)
Translocation t(11;22) in esthesioneuroblastoma.Cancer genetics and cytogenetics, 29 1
H. Webb, C. Griffin (1991)
Cytogenetic study of acoustic neuroma.Cancer genetics and cytogenetics, 56 1
I. Granberg, J. Mark (1971)
The chromosomal aberration of double-minutes in a human embryonic rhabdomyosarcoma.Acta cytologica, 15 1
C. Turc‐Carel, S. Lizard‐Nacol, E. Justrabo, M. Favrot, T. Philip, E. Tabone (1986)
Consistent chromosomal translocation in alveolar rhabdomyosarcoma.Cancer genetics and cytogenetics, 19 3-4
(1983)
Chromosomal translocations in Ewing's sarcoma.The New England journal of medicine, 309 8
E. Douglass, M. Valentine, E. Etcubanas, D. Parham, B. Webber, P. Houghton, J. Houghton, A. Green (1987)
A specific chromosomal abnormality in rhabdomyosarcoma.Cytogenetics and cell genetics, 45 3-4
(1991)
Human gene mapping d l l . Cytogenetic analysis in a series of 56 neurinomas (abstr)
S. Lizard‐Nacol, F. Mugneret, C. Volk, C. Turc‐Carel, M. Favrot, T. Philip (1987)
Translocation (2;13)(q37;q14) in alveolar rhabdomyosarcoma: a new case.Cancer genetics and cytogenetics, 25 2
J. Couturier, Olivier Delattre, Michèle Kujas, Jacques Philippon, M. Peter, Guy Rouleau, A. Aurias, Gilles Thomas (1990)
Assessment of chromosome 22 anomalies in neurinomas by combined karyotype and RFLP analyses.Cancer genetics and cytogenetics, 45 1
G. Stenman, L. Kindblom, L. Angervall (1992)
Reciprocal translocation t(12;22)(q13;q13) in clearcell sarcoma of tendons and aponeurosesGenes, 4
J. Brooks, M. Freeman, H. Enterline (1985)
Malignant “Triton” tumors. Natural history and immunohistochemistry of nine new cases with literature reviewCancer, 55
(1989)
Tissue culture techniques and chromosome preparation
G. Stenman, L. Kindblom, M. Johansson, L. Angervall (1991)
Clonal chromosome abnormalities and in vitro growth characteristics of classical and cellular schwannomas.Cancer genetics and cytogenetics, 57 1
J. Bridge, C. Sreekantaiah, J. Neff, A. Sandberg (1991)
Cytogenetic findings in clear cell sarcoma of tendons and aponeuroses. Malignant melanoma of soft parts.Cancer genetics and cytogenetics, 52 1
(1982)
Alveolar rhahdomyosarcoma: A cytogenetic and correlated cytological and histological study
O. Olopade, J. Rowley (1981)
The Chromosomes in Human Cancer and LeukemiaJAMA, 267
S. Heim, F. Mertens, Yuesheng Jin, N. Mandahl, B. Johansson, A. Biörklund, J. Wennerberg, N. Jonsson, F. Mitelman (1989)
Diverse chromosome abnormalities in squamous cell carcinomas of the skin.Cancer genetics and cytogenetics, 39 1
B. Gladstone, Purvish Parikh, B. Balsara, P. Kadam, S. Rao, Nair Cn, N. Jambekar, Suresh Advani (1993)
Rhabdomyosarcoma. A cytogenetically interesting case report.Cancer genetics and cytogenetics, 66 1
J. Travis, J. Bridge (1992)
Significance of both numerical and structural chromosomal abnormalities in clear cell sarcoma.Cancer genetics and cytogenetics, 64 2
J. Bridge, C. Sreekantaiah, B. Mouron, J. Neff, A. Sandberg, S. Wolman (1992)
Clonal chromosomal abnormalities in desmoid tumors. Implications for histopathogenesisCancer, 69
G. Brodeur, R. Seeger, R. Seeger, M. Schwab, H. Varmus, J. Bishop (1984)
Amplification of N-myc in untreated human neuroblastomas correlates with advanced disease stage.Science, 224 4653
J. Cowan, M. Beckett, N. Tarbell, R. Weichselbaum (1990)
Symmetrical chromosome rearrangements in cell lines established from human radiation-induced sarcomas.Cancer genetics and cytogenetics, 50 1
(1938)
Rhabdomyomas des nerfs
S. Hsu, G. Luk, A. Krush, S. Hamilton, H. Hoover (1983)
Multiclonal origin of polyps in Gardner syndrome.Science, 221 4614
Malignant triton tumor is a rare histologic variant of malignant schwannoma that shows both neural and skeletal muscle differentiation. In this study, cytogenetic analysis of a recurrent malignant triton tumor of the forearm from a 26‐year‐old female and a primary paraspinal malignant triton tumor from a 27‐year‐old female revealed complex karyotypes displaying multiple numercial and structural abnormalities. Abnormalities shared by both tumors included three copies of chromosome 22 and structural rearrangements of chromosomes 2, 7, and 21 at identical or closely located breakpoints. Genes Chrom Cancer 9:1‐7 (1994). © 1994 Wiley‐Liss, Inc.
Genes, Chromosomes and Cancer – Wiley
Published: Jan 1, 1994
Read and print from thousands of top scholarly journals.
Already have an account? Log in
Bookmark this article. You can see your Bookmarks on your DeepDyve Library.
To save an article, log in first, or sign up for a DeepDyve account if you don’t already have one.
Copy and paste the desired citation format or use the link below to download a file formatted for EndNote
Access the full text.
Sign up today, get DeepDyve free for 14 days.
All DeepDyve websites use cookies to improve your online experience. They were placed on your computer when you launched this website. You can change your cookie settings through your browser.