Microduplication 3p26.3p24.3 and 4q34.3q35.2 Microdeletion Identified in a Patient with Developmental Delay Associated with Brain Malformation von Cardos, Georgeta, Gica, Nicolae, Gica, Corina, Panaitescu, Anca Maria, Predescu, Mariana, Peltecu, Gheorghe, Nedelea, Florina Mihaela

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1q44 microdeletion syndrome: A new case with potential additional features von SHELBY, Elena-Silvia, HUSEYINOGLU, Tanser, CARDOS, Georgeta, PADURE, Liliana, MIREA, Andrada, LEANCA, Madalina, BADINA, Mihaela, BARLADEANU, Nadejda, NEDELEA, Florina Mihaela

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Prader-Willy syndrome: heterogenous genetic mechanisms in a wide phenotypic spectrum von Cardos, Georgeta, Dima, Vlad, Predescu, Mariana, Demetrian, Mihaela, Nedelea, Florina Mihaela

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Unusual precocious diagnosis of Duchenne muscular dystrophy by SNP-array in a 6-month old baby von Cardos, Georgeta, Dima, Vlad, Hera, Cristina, Predescu, Mariana, Nedelea, Florina Mihaela

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A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature von Popescu, Roxana, Grămescu, Mihaela, Caba, Lavinia, Pânzaru, Monica-Cristina, Butnariu, Lăcrămioara, Braha, Elena, Popa, Setalia, Rusu, Cristina, Cardos, Georgeta, Zeleniuc, Monica, Martiniuc, Violeta, Gug, Cristina, Păduraru, Luminiţa, Stamatin, Maria, Diaconu, Carmen C, Gorduza, Eusebiu Vlad

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Oculocutaneous albinism associated with multiple malformations and psychomotor retardation von BUDISTEANU, MAGDALENA, ARGHIR, AURORA, CHIRIEAC, SORINA MIHAELA, CARDOS, GEORGETA, LUNGEANU, AGRIPINA

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ANCIENT DNA STUDY ON HUMAN FOSSILS FOUND IN COSTIŞA, ROMANIA, DATING FROM THE BRONZE AGE von CARDOS, Georgeta, RODEWALD, Alexander, SOFICARU, Andrei D

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