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The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 Patients.
Budisteanu M, Papuc SM, Streata I, Cucu M, Pirvu A, Serban-Sosoi S, Erbescu A, Andrei E, Iliescu C, Ioana D, Severin E, Ioana M, Arghir A. Budisteanu M, et al. Among authors: arghir a. Genes (Basel). 2021 Jul 1;12(7):1025. doi: 10.3390/genes12071025. Genes (Basel). 2021. PMID: 34356041 Free PMC article.
Novel clinical finding in MECP2 duplication syndrome.
Budisteanu M, Papuc SM, Tutulan-Cunita A, Budisteanu B, Arghir A. Budisteanu M, et al. Among authors: arghir a. Eur Child Adolesc Psychiatry. 2011 Jul;20(7):373-5. doi: 10.1007/s00787-011-0184-2. Epub 2011 May 18. Eur Child Adolesc Psychiatry. 2011. PMID: 21590509 No abstract available.
18q deletion syndrome - A case report.
Budisteanu M, Arghir A, Chirieac SM, Tutulan-Cunita A, Lungeanu A. Budisteanu M, et al. Among authors: arghir a. Maedica (Bucur). 2010 Apr;5(2):135-8. Maedica (Bucur). 2010. PMID: 21977138 Free PMC article.
3p interstitial deletion: novel case report and review.
Ţuţulan-Cunită AC, Papuc SM, Arghir A, Rötzer KM, Deshpande C, Lungeanu A, Budişteanu M. Ţuţulan-Cunită AC, et al. Among authors: arghir a. J Child Neurol. 2012 Aug;27(8):1062-6. doi: 10.1177/0883073811431016. Epub 2012 Jan 30. J Child Neurol. 2012. PMID: 22290856 Review.
Diagnostic approach of angelman syndrome.
Duca DG, Craiu D, Boer M, Chirieac SM, Arghir A, Tutulan-Cunita A, Barca D, Iliescu C, Lungeanu A, Magureanu S, Budisteanu M. Duca DG, et al. Among authors: arghir a. Maedica (Bucur). 2013 Sep;8(4):321-7. Maedica (Bucur). 2013. PMID: 24790661 Free PMC article.
39 results