The donor chromosome breakpoint for a jumping translocation is associated with large low-copy repeats in 21q21.3

Publisher： Karger

E-ISSN： 1424-859x|101|2|118-123

ISSN： 1424-8581

Source： Cytogenetic and Genome Research, Vol.101, Iss.2, 2003-11, pp. : 118-123

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Dissection of an inverted X(p21.3q27.1) chromosome associated with mental retardation

By  

Cytogenetic and Genome Research, Vol. 101, Iss. 2, 2003-11 ,pp. : 124-129

Karger

Access to resources Recommend Favorite

Intragenic breakpoint within RAD51L1 in a t(6;14)(p21.3;q24) of a pulmonary chondroid hamartoma

By  

Cytogenetic and Genome Research, Vol. 95, Iss. 1-2, 2002-04 ,pp. : 17-19

Karger

Access to resources Recommend Favorite

Extensive nonhomologous meiotic synapsis between normal chromosome axes of an rcp(3;6)(p14;q21) translocation in a hairless Mexican boar

By  

Cytogenetic and Genome Research, Vol. 120, Iss. 1-2, 2008-04 ,pp. : 112-116

Karger

Access to resources Recommend Favorite

MYCN overexpression is associated with unbalanced copy number gain, altered nuclear location, and overexpression of chromosome arm 17q genes in neuroblastoma tumors and cell lines

By  

GENES, CHROMOSOMES AND CANCER, Vol. 54, Iss. 10, 2015-10 ,pp. : 616-628

John Wiley & Sons Inc

Access to resources Recommend Favorite

Cloning and characterization of the breakpoint regions of a chromosome 11;18 translocation in a patient with hamartoma of the retinal pigment epithelium

By  

Cytogenetic and Genome Research, Vol. 91, Iss. 1-4, 2001-01 ,pp. : 141-147

Karger

Access to resources Recommend Favorite