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A de novo 2.3 Mb deletion in 2q24.2q24.3 in a 20-month-old developmentally delayed girl.
Gene. 2014 Apr 10;539(1):168-72. doi: 10.1016/j.gene.2014.01.060. Epub 2014 Feb 4.
Gene. 2014.
PMID: 24508274
Ambras syndrome: report on two affected siblings with no prior family history.
Belengeanu V, Rozsnyai K, Gug C, Bănăţeanu M, Farcaş S, Belengeanu A.
Belengeanu V, et al. Among authors: belengeanu a.
Clin Dysmorphol. 2004 Oct;13(4):265-267.
Clin Dysmorphol. 2004.
PMID: 15365467
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Assessment of p53 and HER-2/neu genes status and protein products in oral squamous cell carcinomas.
Stoicănescu D, Andreescu N, Belengeanu A, Meszaros N, Cornianu M.
Stoicănescu D, et al. Among authors: belengeanu a.
Rom J Morphol Embryol. 2013;54(4):1107-13.
Rom J Morphol Embryol. 2013.
PMID: 24399009
Free article.
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A comprehensive evaluation of an OFDI syndrome from child to teenager.
Belengeanu V, Marian D, Hosszu T, Ogodescu AS, Belengeanu AD, Samoilă C, Freiman P, Lile IE.
Belengeanu V, et al. Among authors: belengeanu ad.
Rom J Morphol Embryol. 2019;60(2):697-706.
Rom J Morphol Embryol. 2019.
PMID: 31658347
Free article.
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Amplification of HER-2 gene in breast cancer: immunohistochemical and FISH assessment.
Belengeanu A, Mureşan A, Stoicănescu D, Lazăr E.
Belengeanu A, et al.
Rom J Morphol Embryol. 2010;51(2):321-6.
Rom J Morphol Embryol. 2010.
PMID: 20495751
Free article.
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