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BioMed Research International
Volume 2015, Article ID 341986, 8 pages
http://dx.doi.org/10.1155/2015/341986
Research Article

In Pursuit of New Imprinting Syndromes by Epimutation Screening in Idiopathic Neurodevelopmental Disorder Patients

Unidad de Genética y Diagnóstico Prenatal, Hospital Universitario y Politécnico La Fe, Avenida de Campanar 21, 46009 Valencia, Spain

Received 21 October 2014; Revised 4 May 2015; Accepted 11 May 2015

Academic Editor: Marco Fichera

Copyright © 2015 Sonia Mayo 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.

Citations to this Article [1 citation]

The following is the list of published articles that have cited the current article.

  • Antonio D. Hidalgo-Santos, Maria del Carmen DeMingo-Alemany, Francisca Moreno-Macián, Mónica Roselló, Carmen Orellana, Francisco Martínez, Alfonso Caro-Llopis, Sara León-Cariñena, and Miguel Tomás-Vila, “A Novel Mutation of MAGEL2 in a Patient with Schaaf-Yang Syndrome and Hypopituitarism,” International Journal of Endocrinology and Metabolism, vol. InPress, no. InPress, 2018. View at Publisher · View at Google Scholar