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Results: 1 to 20 of 31

1.

Heterogeneity of PLAG1 gene rearrangements in pleomorphic adenoma.

Kandasamy J, Smith A, Diaz S, Rose B, O'Brien C.

Cancer Genet Cytogenet. 2007 Aug;177(1):1-5.

PMID:
17693184
[PubMed - indexed for MEDLINE]
2.

First insights into the molecular basis of pleomorphic adenomas of the salivary glands.

Voz ML, Van de Ven WJ, Kas K.

Adv Dent Res. 2000 Dec;14:81-3. Review.

PMID:
11842929
[PubMed - indexed for MEDLINE]
3.

[Molecular techniques lead to the first insights into the pathophysiology of salivary gland adenomas].

Kas K.

Verh K Acad Geneeskd Belg. 2001;63(1):35-40. Review. Dutch.

PMID:
11284386
[PubMed - indexed for MEDLINE]
4.

Chromosome rearrangements in cornelia de Lange syndrome (CdLS): report of a der(3)t(3;12)(p25.3;p13.3) in two half sibs with features of CdLS and review of reported CdLS cases with chromosome rearrangements.

DeScipio C, Kaur M, Yaeger D, Innis JW, Spinner NB, Jackson LG, Krantz ID.

Am J Med Genet A. 2005 Sep 1;137A(3):276-82. Review.

PMID:
16075459
[PubMed - indexed for MEDLINE]
5.
6.

Concurrent cytogenetic, interphase fluorescence in situ hybridization and DNA flow cytometric analyses of a carcinoma ex-pleomorphic adenoma of parotid gland.

el-Naggar AK, Lovell M, Callender DL, Ordonez NG, Killary AM.

Cancer Genet Cytogenet. 1998 Dec;107(2):132-6. Review.

PMID:
9844608
[PubMed - indexed for MEDLINE]
7.

PLAG1, the prototype of the PLAG gene family: versatility in tumour development (review).

Van Dyck F, Declercq J, Braem CV, Van de Ven WJ.

Int J Oncol. 2007 Apr;30(4):765-74. Review.

PMID:
17332914
[PubMed - indexed for MEDLINE]
8.

The role of cytogenetics in the classification of soft tissue tumours.

Dei Tos AP, Dal Cin P.

Virchows Arch. 1997 Aug;431(2):83-94. Review.

PMID:
9293889
[PubMed - indexed for MEDLINE]
9.

Two cases of deletion 5p syndrome: one with paternal involvement and another with atypical presentation.

Azman BZ, Akhir SM, Zilfalil BA, Ankathil R.

Singapore Med J. 2008 Apr;49(4):e98-e100. Review.

PMID:
18418516
[PubMed - indexed for MEDLINE]
Free Article
10.

Interstitial deletion of chromosome 4, del(4)(q12q21.1), in a mentally retarded boy with a piebald trait, due to maternal insertion, ins(8;4).

Fujimoto A, Reddy KS, Spinks R.

Am J Med Genet. 1998 Jan 6;75(1):78-81. Review.

PMID:
9450862
[PubMed - indexed for MEDLINE]
11.

Molecular cytogenetic characterization of pancreas cancer cell lines reveals high complexity chromosomal alterations.

Griffin CA, Morsberger L, Hawkins AL, Haddadin M, Patel A, Ried T, Schrock E, Perlman EJ, Jaffee E.

Cytogenet Genome Res. 2007;118(2-4):148-56. Review.

PMID:
18000365
[PubMed - indexed for MEDLINE]
12.

Clustering of deletions on chromosome 13 in benign and low-malignant lipomatous tumors.

Dahlén A, Debiec-Rychter M, Pedeutour F, Domanski HA, Höglund M, Bauer HC, Rydholm A, Sciot R, Mandahl N, Mertens F.

Int J Cancer. 2003 Feb 20;103(5):616-23. Review.

PMID:
12494468
[PubMed - indexed for MEDLINE]
13.

[Report of a case of hybrid acute leukemia with t (12; 22) and literature review].

Hu XX, Gong SL, Song XM, Chen L, Qiu HY, Gao L, Wang JM.

Zhonghua Xue Ye Xue Za Zhi. 2006 May;27(5):331-4. Review. Chinese.

PMID:
16875585
[PubMed - indexed for MEDLINE]
14.

Molecular cytogenetics of t(X;1)(p11.2;q21) with complex rearrangements in a renal cell carcinoma.

Zattara-Cannoni H, Daniel L, Roll P, Coulange C, Vagner-Capodano A.

Cancer Genet Cytogenet. 2000 Nov;123(1):61-4. Review.

PMID:
11120337
[PubMed - indexed for MEDLINE]
15.

Complex rearrangement of chromosomes 19, 21, and 22 in Ewing sarcoma involving a novel reciprocal inversion-insertion mechanism of EWS-ERG fusion gene formation: a case analysis and literature review.

Maire G, Brown CW, Bayani J, Pereira C, Gravel DH, Bell JC, Zielenska M, Squire JA.

Cancer Genet Cytogenet. 2008 Mar;181(2):81-92. doi: 10.1016/j.cancergencyto.2007.11.002. Review.

PMID:
18295659
[PubMed - indexed for MEDLINE]
16.

RUNX1-MTG16 fusion gene in acute myeloblastic leukemia with t(16;21)(q24;q22): case report and review of the literature.

De Braekeleer E, Douet-Guilbert N, Le Bris MJ, Morel F, Férec C, De Braekeleer M.

Cancer Genet Cytogenet. 2008 Aug;185(1):47-50. doi: 10.1016/j.cancergencyto.2008.04.011. Review.

PMID:
18656694
[PubMed - indexed for MEDLINE]
17.

FOXC1 gene deletion is associated with eye anomalies in ring chromosome 6.

Zhang HZ, Li P, Wang D, Huff S, Nimmakayalu M, Qumsiyeh M, Pober BR.

Am J Med Genet A. 2004 Jan 30;124A(3):280-7. Review.

PMID:
14708101
[PubMed - indexed for MEDLINE]
18.

Cytogenetic and molecular observations in human and experimental salivary gland tumors.

Sandros J, Stenman G, Mark J.

Cancer Genet Cytogenet. 1990 Feb;44(2):153-67. Review.

PMID:
2153439
[PubMed - indexed for MEDLINE]
19.

Case of lipoblastoma with two derivative chromosomes 8 containing homogeneously staining-like regions and a review of the literature: lipoblastoma and chromosome 8.

Batanian JR, Brink DS, Thorpe CM, Haddad BR.

Cancer Genet Cytogenet. 2001 Feb;125(1):10-3. Review.

PMID:
11297761
[PubMed - indexed for MEDLINE]
20.

Aggressive angiomyxoma with t(12;21) and HMGA2 rearrangement: report of a case and review of the literature.

Rawlinson NJ, West WW, Nelson M, Bridge JA.

Cancer Genet Cytogenet. 2008 Mar;181(2):119-24. doi: 10.1016/j.cancergencyto.2007.11.008. Review.

PMID:
18295664
[PubMed - indexed for MEDLINE]
Free PMC Article
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