De novo 15.5-Mb interstitial deletion in 5p in a male ascertained by Oligospermia

0Citations
Citations of this article
6Readers
Mendeley users who have this article in their library.
Get full text

Abstract

We describe a case of a 34-year-old male presenting with oligospermia and an otherwise normal phenotype. Investigation with array-based comparative genomic hybridization (aCGH) revealed an interstitial deletion of about 15.5 Mb in chromosome 5p13.3p14.3. We compared the phenotype of our patient with recently reported patients studied by aCGH, who show an overlapping deletion. We also analyzed the gene content of the deleted region in order to propose a possible involvement of specific genes in the clinical phenotype. Copyright © 2013 S. Karger AG, Basel.

Cite

CITATION STYLE

APA

Papoulidis, I., Vetro, A., Kefalas, K., Orru, S., Thomaidis, L., Iliodromiti, Z., … Manolakos, E. (2013). De novo 15.5-Mb interstitial deletion in 5p in a male ascertained by Oligospermia. Molecular Syndromology, 4(5), 250–254. https://doi.org/10.1159/000351656

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