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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.

Supplementary Material

Table 1: PCR conditions, primer sequences and reagents employed for the methylation test. Note that the PCR are mounted in duplicate with and without the addition of HpaII methylation-sensitive enzyme.

Table 2: PCR conditions, primer sequences and reagents employed for amplification of microsatellite markers used to evaluate the uniparental disomy by segregation analysis in the family (patient and parents).

  1. Supplementary Materials