COMPREHENSIVE GENETIC EVALUATION OF BULGARIAN CHILDREN WITH SYNDROMIC CRANIOSYNOSTOSIS
Delchev T.1, Hadjidekova S.2, Bichev S.3, Veleva Ts.1, Boneva I.4, Avdjieva-Tzavella D.1
*Corresponding Author: Trayan Delchev, MD, PhD, Department of Clinical genetics, University Children Hospital, Medical University of Sofia; Sofia, Bulgaria, Ivan Geshov blvd. No 11, tel: +359883482376, e-mail: trayan_delchev@abv.bg
page: 6

AKNOWLEDMENTS

Declaration of Interest: The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this article. Ethics approval: All procedures performed in this study involving human participants were in accordance with the ethical standarts of the institutional research comitee and with the 1964 Helsinki Decladarion and its later amendments of comparable ethical standarts. The study was approved by the Ethics Commitee of Medical Unversity of Sofia. Consent to participate and for publication: Informed consent was obtained from all participants, including their respective family members (and/or legal guardians) before clinical selection was performed. Author‘s contributions: main author, corresponding author, preliminary clinical selection and diagnostics - T. Delchev; DNA extraction, array CGH screening, array analysis - S. Hadjidekova; DNA extraction, MLPA screening - S. Bichev; imaging studies documentation - Ts. Veleva; conventional cytogenetic analysis - I. Boneva; coordinator, main consultant, academic science advisor - D. Avdjieva-Tzavella



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