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Items: 1 to 20 of 765

1.

Centromeric alpha-satellite DNA break in reciprocal translocations.

Wang JC, Hajianpour A, Habibian R.

Cytogenet Genome Res. 2009;125(4):329-33. doi: 10.1159/000235939. Epub 2009 Oct 27.

PMID:
19864896
3.

Breakpoints in Robertsonian translocations are localized to satellite III DNA by fluorescence in situ hybridization.

Gravholt CH, Friedrich U, Caprani M, Jørgensen AL.

Genomics. 1992 Dec;14(4):924-30.

PMID:
1478673
5.

Evidence for structural heterogeneity from molecular cytogenetic analysis of dicentric Robertsonian translocations.

Sullivan BA, Jenkins LS, Karson EM, Leana-Cox J, Schwartz S.

Am J Hum Genet. 1996 Jul;59(1):167-75.

6.
8.

Identification of the origin of centromeres in whole-arm translocations using fluorescent in situ hybridization with alpha-satellite DNA probes.

Tharapel AT, Qumsiyeh MB, Martens PR, Tharapel SA, Dalton JD, Ward JC, Wilroy RS Jr.

Am J Med Genet. 1991 Jul 1;40(1):117-20.

PMID:
1887840
9.

Cytogenetic findings in a breast stromal sarcoma. Application of fluorescence in situ hybridization to characterize the breakpoint regions in an 11;19 translocation.

Garcia-Palazzo IE, Palazzo JP, Liu ZM, Taguchi T, Testa JR.

Cancer Genet Cytogenet. 1992 Oct 1;63(1):47-51.

PMID:
1423226
10.

Structure of DNA near long tandem arrays of alpha satellite DNA at the centromere of human chromosome 7.

Wevrick R, Willard VP, Willard HF.

Genomics. 1992 Dec;14(4):912-23.

PMID:
1478672
13.
15.

dic(9;20): a new recurrent chromosome abnormality in adult acute lymphoblastic leukemia.

Rieder H, Schnittger S, Bodenstein H, Schwonzen M, Wörmann B, Berkovic D, Ludwig WD, Hoelzer D, Fonatsch C.

Genes Chromosomes Cancer. 1995 May;13(1):54-61.

PMID:
7541644
16.

[Study of alpha-satellite DNA in cosmid libraries, specific for chromosomes 13, 21, and 22, using fluorescence in situ hybridization].

Solov'ev IV, Iurov IuB, Vorsanova SG, Marcais B, Rogaev EI, Kapanadze BI, Brodianskiĭ VM, Iankovskiĭ NK, Roizes G.

Genetika. 1998 Nov;34(11):1470-9. Russian.

PMID:
10096024
17.

Prenatal diagnosis and characterization of an unbalanced whole arm translocation resulting in monosomy for 18p.

McGhee EM, Qu Y, Wohlferd MM, Goldberg JD, Norton ME, Cotter PD.

Clin Genet. 2001 Apr;59(4):274-8.

PMID:
11298684
19.
20.

Molecular cytogenetic characterization of 18;21 whole arm translocation associated with monosomy 18p.

Wang JC, Nemana L, Kou SY, Habibian R, Hajianpour MJ.

Am J Med Genet. 1997 Sep 5;71(4):463-6.

PMID:
9286456
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