Molecular cytogenetic characteristics of Down syndrome newborns

8Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.

Your institution provides access to this article.

Abstract

Down syndrome (DS) is a multifactorial disorder with a high predisposition to leukemia and other malignancies. A change in the replication pattern from synchronous in normal genes to asynchronous in DS amniocytes has previously been reported. The objective of this study was to evaluate additional molecular cytogenetic factors which could re-emphasize the high correlation between DS cells and genetic instability. We found a higher rate of random aneuploidy in chromosomes 9 and 18 and a higher rate of asynchronous replication in the subtelomeric region or DS leukocytes than in cells from normal newborns. In addition, the telomere capture phenomenon was observed in the DS leukocytes but not in normal controls. The molecular cytogenetic factors observed in the DS individuals are known to correlate with genomic instability and with predisposition to cancer. © The Japan Society of Human Genetics and Springer-Verlag 2006.

Cite

CITATION STYLE

APA

Amiel, A., Goldzak, G., Gaber, E., & Fejgin, M. D. (2006). Molecular cytogenetic characteristics of Down syndrome newborns. Journal of Human Genetics, 51(6), 541–547. https://doi.org/10.1007/s10038-006-0395-4

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free