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Expanding the Clinical Phenotype of 19q Interstitial Deletions: A New Case with 19q13.32-q13.33 Deletion and Short Review of the Literature by Elena-Silvia Shelby, Michael Morris, Liliana Pădure, Andrada Mirea, Relu Cocoș, Alexandru Cărămizaru, Simona Șerban-Sosoi, Andrei Pîrvu, Ioana Streață
Published 2022-01-01
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The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 Patients by Magdalena Budisteanu, Sorina Mihaela Papuc, Ioana Streata, Mihai Cucu, Andrei Pirvu, Simona Serban-Sosoi, Alina Erbescu, Emanuela Andrei, Catrinel Iliescu, Doina Ioana, Emilia Severin, Mihai Ioana, Aurora Arghir
Published 2021-07-01
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Cytogenetic Analysis of Sporadic First-Trimester Miscarriage Specimens Using Karyotyping and QF-PCR: A Retrospective Romanian Cohort Study by Gabriela Popescu-Hobeanu, Anca-Lelia Riza, Ioana Streață, Ștefania Tudorache, Alexandru Comănescu, Florentina Tănase, Roxana Cristina Drăgușin, Cornelia Pascu, Anda Lorena Dijmărescu, Monica-Laura Cara, Ștefania Dorobanțu, Bianca Petre-Mandache, Mihai Cucu, Simona Serban Sosoi, Mihai Ioana, Dominic Iliescu, Florin Burada
Published 2022-11-01
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Pathogenic Copy Number Variations Involved in the Genetic Etiology of Syndromic and Non-Syndromic Intellectual Disability—Data from a Romanian Cohort by Ioana Streață, Alexandru Caramizaru, Anca-Lelia Riza, Simona Șerban-Sosoi, Andrei Pîrvu, Monica-Laura Cara, Mihai-Gabriel Cucu, Amelia Mihaela Dobrescu, Ro-NMCA-ID Group, CExBR Pediatric Neurology Obregia Group, CExBR Pediatric Neurology “V. Gomoiu” Hospital Group, Elena-Silvia Shelby, Adriana Albeanu, Florin Burada, Mihai Ioana
Published 2022-12-01
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