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Case Reports in Genetics
Volume 2014, Article ID 470830, 5 pages
http://dx.doi.org/10.1155/2014/470830
Case Report

A New Case of 13q12.2q13.1 Microdeletion Syndrome Contributes to Phenotype Delineation

1Medical Genetics Unit, “San Luigi Gonzaga” University Hospital, University of Torino, Regione Gonzole 10, 10143 Orbassano, Italy
2Department of Clinical & Biological Sciences, University of Torino, 10143 Orbassano, Italy
3Department of Medical Sciences, University of Torino, Via Santena 19, 10126 Torino, Italy
4Medical Genetics, “Città della Salute e della Scienza” University Hospital, 10126 Torino, Italy

Received 4 August 2014; Accepted 2 November 2014; Published 23 November 2014

Academic Editor: Evica Rajcan-Separovic

Copyright © 2014 Giorgia Mandrile et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Giorgia Mandrile, Eleonora Di Gregorio, Alessandro Calcia, et al., “A New Case of 13q12.2q13.1 Microdeletion Syndrome Contributes to Phenotype Delineation,” Case Reports in Genetics, vol. 2014, Article ID 470830, 5 pages, 2014. https://doi.org/10.1155/2014/470830.