Array CGH - A Powerful Tool in Molecular Diagnostic of Pathogenic Microdeletions - Williams-Beuren Syndrome - A Case Report by Streață, I, Șerban-Șoșoi, S, Budișteanu, M, Pîrvu, A, Burada, F, Mixich, F, Ioana, M

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P140Clinical caracterization of a new case with chromosome 3 terminal microdeletion, involving chl1 gene by Focsa, I O, Ioana, M, Streata, I, Sosoi, S Serban, Pirvu, A, Bohiltea, L C, Budisteanu, M

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P140 Clinical caracterization of a new case with chromosome 3 terminal microdeletion, involving chl1 gene by Focsa, IO, Ioana, M, Streata, I, Sosoi, S Serban, Pirvu, A, Bohiltea, LC, Budisteanu, M

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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 Streață, Ioana, Caramizaru, Alexandru, Riza, Anca-Lelia, Șerban-Sosoi, Simona, Pîrvu, Andrei, Cara, Monica-Laura, Cucu, Mihai-Gabriel, Dobrescu, Amelia Mihaela, Ro-Nmca-Id Group, CExBR Pediatric Neurology Obregia Group, CExBR Pediatric Neurology V Gomoiu Hospital Group, Shelby, Elena-Silvia, Albeanu, Adriana, Burada, Florin, Ioana, Mihai

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Impact of Intermediate Hyperglycemia and Diabetes on Immune Dysfunction in Tuberculosis by Eckold, Clare, Kumar, Vinod, Weiner, January, Alisjahbana, Bachti, Riza, Anca-Lelia, Ronacher, Katharina, Coronel, Jorge, Kerry-Barnard, Sarah, Malherbe, Stephanus T, Kleynhans, Leanie, Stanley, Kim, Ruslami, Rovina, Ioana, Mihai, Ugarte-Gil, Cesar, Walzl, Gerhard, van Crevel, Reinout, Wijmenga, Cisca, Critchley, Julia A, Dockrell, Hazel M, Cliff, Jacqueline M

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The Value of Parental Karyotyping in Recurrent Pregnancy Loss Lies in Individual Risk Assessments by Popescu-Hobeanu, Gabriela, Serban Sosoi, Simona, Cucu, Mihai, Streață, Ioana, Dobrescu, Amelia, Pleșea, Răzvan, Costache, Anca Lelia, Iordache, Andreea, Petre-Mandache, Bianca, Tudorache, Ștefania, Comănescu, Alexandru, Iliescu, Dominic, Burada, Florin

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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 Shelby, Elena-Silvia, Morris, Michael, Pădure, Liliana, Mirea, Andrada, Cocoș, Relu, Cărămizaru, Alexandru, Șerban-Sosoi, Simona, Pîrvu, Andrei, Streață, Ioana

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Prenatal diagnosis of a pure 15q distal trisomy derived from a maternal pericentric inversion: A case report by Burada, Florin, Streata, Ioana, Ungureanu, Anda, Ruican, Dan, Nagy, Rodica, Serban-Sosoi, Simona, Stambouli, Danai, Dimos, Luiza, Popescu-Hobeanu, Gabriela, Mihai, Ioana, Iliescu, Dominic

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The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 Patients by Budisteanu, Magdalena, Papuc, Sorina Mihaela, Streata, Ioana, Cucu, Mihai, Pirvu, Andrei, Serban-Sosoi, Simona, Erbescu, Alina, Andrei, Emanuela, Iliescu, Catrinel, Ioana, Doina, Severin, Emilia, Ioana, Mihai, Arghir, Aurora

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Cytogenetic Analysis of Sporadic First-Trimester Miscarriage Specimens Using Karyotyping and QF-PCR: A Retrospective Romanian Cohort Study by Popescu-Hobeanu, Gabriela, Riza, Anca-Lelia, Streață, Ioana, Tudorache, Ștefania, Comănescu, Alexandru, Tănase, Florentina, Drăgușin, Roxana Cristina, Pascu, Cornelia, Dijmărescu, Anda Lorena, Cara, Monica-Laura, Dorobanțu, Ștefania, Petre-Mandache, Bianca, Cucu, Mihai, Sosoi, Simona Serban, Ioana, Mihai, Iliescu, Dominic, Burada, Florin

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