Format
Items per page
Sort by

Send to:

Choose Destination

Links from PubMed

Items: 1 to 20 of 205

1.

Translocation der(13;21)(q10;q10) in skeletal and extraskeletal mesenchymal chondrosarcoma.

Naumann S, Krallman PA, Unni KK, Fidler ME, Neff JR, Bridge JA.

Mod Pathol. 2002 May;15(5):572-6. Review.

2.

Cytogenetic and spectral karyotype analyses of benign and malignant cartilage tumours.

Sjögren H, Orndal C, Tingby O, Meis-Kindblom JM, Kindblom LG, Stenman G.

Int J Oncol. 2004 Jun;24(6):1385-91.

PMID:
15138578
3.

Trisomy 8 as the sole cytogenetic abnormality in a case of extraskeletal mesenchymal chondrosarcoma.

Gatter KM, Olson S, Lawce H, Rader AE.

Cancer Genet Cytogenet. 2005 Jun;159(2):151-4.

PMID:
15899388
4.

Mesenchymal chondrosarcoma. A cytogenetic, immunohistochemical and ultrastructural study.

Dobin SM, Donner LR, Speights VO Jr.

Cancer Genet Cytogenet. 1995 Aug;83(1):56-60.

PMID:
7656206
5.

A mesenchymal chondrosarcoma of a child with the reciprocal translocation (11;22)(q24;q12).

Sainati L, Scapinello A, Montaldi A, Bolcato S, Ninfo V, Carli M, Basso G.

Cancer Genet Cytogenet. 1993 Dec;71(2):144-7.

PMID:
8281518
6.

Robertsonian translocations--reproductive risks and indications for preimplantation genetic diagnosis.

Scriven PN, Flinter FA, Braude PR, Ogilvie CM.

Hum Reprod. 2001 Nov;16(11):2267-73.

7.

der(11)t(11;17): a distinct cytogenetic pathway of advanced stage neuroblastoma (NBL) - detected by spectral karyotyping (SKY).

Stark B, Jeison M, Glaser-Gabay L, Bar-Am I, Mardoukh J, Ash S, Atias D, Stein J, Zaizov R, Yaniv I.

Cancer Lett. 2003 Jul 18;197(1-2):75-9. Review.

PMID:
12880963
8.

Familial whole-arm translocations (1;19), (9;13), and (12;21): a review of 101 constitutional exchanges.

Vázquez-Cárdenas A, Vásquez-Velásquez AI, Barros-Núñez P, Mantilla-Capacho J, Rocchi M, Rivera H.

J Appl Genet. 2007;48(3):261-8.

PMID:
17666779
9.

Derivative (1;18)(q10;q10): a recurrent and novel unbalanced translocation involving 1q in myeloid disorders.

Wan TS, Ma SK, Au WY, Chan LC.

Cancer Genet Cytogenet. 2001 Jul 1;128(1):35-8.

PMID:
11454427
10.

Interchromosomal effect in sperm of males with translocations: report of 6 cases and review of the literature.

Douet-Guilbert N, Bris MJ, Amice V, Marchetti C, Delobel B, Amice J, Braekeleer MD, Morel F.

Int J Androl. 2005 Dec;28(6):372-9. Review.

PMID:
16300670
11.

Skeletal and extraskeletal myxoid chondrosarcoma: related or distinct tumors?

Rubin BP, Fletcher JA.

Adv Anat Pathol. 1999 Jul;6(4):204-12.

PMID:
10410173
12.

Chromosomal segregation in spermatozoa of 14 Robertsonian translocation carriers.

Ogur G, Van Assche E, Vegetti W, Verheyen G, Tournaye H, Bonduelle M, Van Steirteghem A, Liebaers I.

Mol Hum Reprod. 2006 Mar;12(3):209-15. Epub 2006 Mar 8.

13.

Cytogenetic analysis in 61 couples with spontaneous abortions.

Jiang J, Fu M, Wang D.

Chin Med J (Engl). 2001 Feb;114(2):200-1.

PMID:
11780207
14.

Translocations involving chromosomes 2 and 13 in benign and malignant cartilaginous neoplasms.

Bridge JA, Sanger WG, Neff JR.

Cancer Genet Cytogenet. 1989 Mar;38(1):83-8.

PMID:
2713817
15.

Translocation (9;22)(q22;q12). A recurrent chromosome abnormality in extraskeletal myxoid chondrosarcoma.

Hirabayashi Y, Ishida T, Yoshida MA, Kojima T, Ebihara Y, Machinami R, Ikeuchi T.

Cancer Genet Cytogenet. 1995 May;81(1):33-7.

PMID:
7773957
16.

Fluorescence in situ hybridization is a useful ancillary diagnostic tool for extraskeletal myxoid chondrosarcoma.

Wang WL, Mayordomo E, Czerniak BA, Abruzzo LV, Dal Cin P, Araujo DM, Lev DC, López-Terrada D, Lazar AJ.

Mod Pathol. 2008 Nov;21(11):1303-10. doi: 10.1038/modpathol.2008.114. Epub 2008 Jun 27.

17.

Chromosome aberrations and HEY1-NCOA2 fusion gene in a mesenchymal chondrosarcoma.

Panagopoulos I, Gorunova L, Bjerkehagen B, Boye K, Heim S.

Oncol Rep. 2014 Jul;32(1):40-4. doi: 10.3892/or.2014.3180. Epub 2014 May 15.

18.

Evidence by spectral karyotyping that 8q11.2 is nonrandomly involved in lipoblastoma.

Chen Z, Coffin CM, Scott S, Meloni-Ehrig A, Shepard R, Issa B, Forsyth DR, Sandberg AA, Brothman AR, Lowichik A.

J Mol Diagn. 2000 May;2(2):73-7.

19.

Down syndrome with partial trisomy of chromosome 21 because of a de-novo unbalanced translocation t(13;21)(q10;q22).

Maciejewski E, Vigneron J, Lambert L, Bonnet C, Hascoët JM.

Clin Dysmorphol. 2012 Oct;21(4):200-3. doi: 10.1097/MCD.0b013e32835909cc. No abstract available.

PMID:
22932442
20.

Cytogenetic findings in clear cell chondrosarcoma.

Nishio J, Reith JD, Ogose A, Maale G, Neff JR, Bridge JA.

Cancer Genet Cytogenet. 2005 Oct 1;162(1):74-7.

PMID:
16157204
Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk