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Items: 1 to 20 of 145

1.

Spindle-cell rhabdomyosarcoma with 2q36 approximately q37 involvement.

Debiec-Rychter M, Hagemeijer A, Sciot R.

Cancer Genet Cytogenet. 2003 Jan 1;140(1):62-5.

PMID:
12550761
2.

Embryonal rhabdomyosarcoma with a der(16)t(1;16) translocation.

Kapels KM, Nishio J, Zhou M, Qualman SJ, Bridge JA.

Cancer Genet Cytogenet. 2007 Apr 1;174(1):68-73.

PMID:
17350470
3.

Detection of the t(2;13)(q35;q14) and PAX3-FKHR fusion in alveolar rhabdomyosarcoma by fluorescence in situ hybridization.

Biegel JA, Nycum LM, Valentine V, Barr FG, Shapiro DN.

Genes Chromosomes Cancer. 1995 Mar;12(3):186-92.

PMID:
7536457
4.

Adult sclerosing rhabdomyosarcoma: cytogenetic link with embryonal rhabdomyosarcoma.

Croes R, Debiec-Rychter M, Cokelaere K, De Vos R, Hagemeijer A, Sciot R.

Virchows Arch. 2005 Jan;446(1):64-7. Epub 2004 Nov 17.

PMID:
15660283
5.

Alveolar rhabdomyosarcoma of the paranasal sinuses in a 57-year-old woman with 1:16 translocation.

Manucha V, Castellani R, Sun CC.

Int J Surg Pathol. 2006 Jul;14(3):238-42.

PMID:
16959712
6.

Embryonal rhabdomyosarcoma with a novel t(2;6)(p23;p21.1).

Pressey JG, Mroczek-Musulman E, Murata-Collins JL, Saito JM, Hammers Y.

Cancer Genet Cytogenet. 2008 Nov;187(1):39-42. doi: 10.1016/j.cancergencyto.2008.07.007.

PMID:
18992640
7.

A variant (2;13) translocation in rhabdomyosarcoma.

Dal Cin P, Brock P, Aly MS, Casteels-Van Daele M, De Wever I, Van Damme B, Van den Berghe H.

Cancer Genet Cytogenet. 1991 Sep;55(2):191-5.

PMID:
1933821
8.

An endometrial polyp with a rearrangement of HMGI-C underlying a complex cytogenetic rearrangement involving chromosomes 2 and 12.

Bol S, Wanschura S, Thode B, Deichert U, Van de Ven WJ, Bartnitzke S, Bullerdiek J.

Cancer Genet Cytogenet. 1996 Aug;90(1):88-90.

PMID:
8780755
9.

Chromosome abnormalities in a primary adult embryonal rhabdomyosarcoma of the prostate.

Middel P, Gunawan B, Gross AJ, Radzun HJ, Füzesi L.

Histopathology. 2000 Oct;37(4):378-80. No abstract available.

PMID:
11184186
10.

A de nevo complex t(7;13;8) translocation with a deletion in the TRPS gene region.

Brandt CA, Lüdecke HJ, Hindkjaer J, Strømkjaer H, Pinkel D, Herlin T, Bolund L, Friedrich U.

Hum Genet. 1997 Sep;100(3-4):334-8.

PMID:
9272151
11.

Fibroadenoma of the breast showing a translocation (6;14), a ring chromosome and two markers involving parts of chromosome 11.

Leuschner E, Meyer-Bolte K, Caselitz J, Bartnitzke S, Bullerdiek J.

Cancer Genet Cytogenet. 1994 Sep;76(2):145-7.

PMID:
7923065
12.

Translocation (2;8)(q35;q13): a recurrent abnormality in congenital embryonal rhabdomyosarcoma.

Meloni-Ehrig A, Smith B, Zgoda J, Greenberg J, Perdahl-Wallace E, Zaman S, Mowrey P.

Cancer Genet Cytogenet. 2009 May;191(1):43-5. doi: 10.1016/j.cancergencyto.2009.01.010.

PMID:
19389508
13.

der(16)t(1;16)(q21;q13) as a secondary change in alveolar rhabdomyosarcoma. A case report and review of the literature.

McManus AP, Min T, Swansbury GJ, Gusterson BA, Pinkerton CR, Shipley JM.

Cancer Genet Cytogenet. 1996 Apr;87(2):179-81.

PMID:
8625268
14.

Variant translocations of chromosome 13 in alveolar rhabdomyosarcoma.

Douglass EC, Rowe ST, Valentine M, Parham DM, Berkow R, Bowman WP, Maurer HM.

Genes Chromosomes Cancer. 1991 Nov;3(6):480-2.

PMID:
1777415
15.

Use of a novel FISH assay on paraffin-embedded tissues as an adjunct to diagnosis of alveolar rhabdomyosarcoma.

Nishio J, Althof PA, Bailey JM, Zhou M, Neff JR, Barr FG, Parham DM, Teot L, Qualman SJ, Bridge JA.

Lab Invest. 2006 Jun;86(6):547-56.

16.

[Alveolar rhabdomyosarcoma with massive bone marrow involvement and 2;13 chromosome translocation].

Naito H, de Higa EH, Kobayashi R, Shikano T, Ishikawa Y, Nojima T.

Rinsho Ketsueki. 1992 Feb;33(2):238-43. Japanese.

PMID:
1635176
17.

Rubinstein-Taybi syndrome with de novo reciprocal translocation t(2;16)(p13.3;p13.3).

Imaizumi K, Kuroki Y.

Am J Med Genet. 1991 Mar 15;38(4):636-9.

PMID:
2063911
18.

Cryptic subtelomeric translocation t(2;16)(q37;q24) segregating in a family with unexplained stillbirths and a dysmorphic, slightly retarded child.

Giardino D, Finelli P, Gottardi G, Clerici D, Mosca F, Briscioli V, Larizza L.

Eur J Hum Genet. 2001 Dec;9(12):881-6.

19.

Molecular cytogenetic analysis of follicular lymphoma (FL) provides detailed characterization of chromosomal instability associated with the t(14;18)(q32;q21) positive and negative subsets and histologic progression.

Nanjangud G, Rao PH, Teruya-Feldstein J, Donnelly G, Qin J, Mehra S, Jhanwar SC, Zelenetz AD, Chaganti RS.

Cytogenet Genome Res. 2007;118(2-4):337-44.

PMID:
18000388
20.

Trisomy 1q, 2, and 20 in a case of hepatoblastoma: possible significance of 2q35-q37 and 1q12-q21 rearrangements.

Yeh YA, Rao PH, Cigna CT, Middlesworth W, Lefkowitch JH, Murty VV.

Cancer Genet Cytogenet. 2000 Dec;123(2):140-3. Review.

PMID:
11150606

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