CHROMOSOMAL ABNORMALITIES IN PATIENTS WITH RECURRENT MISCARRIAGE

by Daniela Mierla, Viorica Radoi, Veronica Stoian
Published 2012-06-01

GENETIC FACTORS INVOLVED IN THE DEVELOPMENT OF CLEFT LIP AND/OR PALATE

by Andrei Kozma, Doriana Agop Forna, Viorica Rădoi, Radu Ursu, Laurențiu Camil Bohâlțea
Published 2019-02-01

ISOLATED DENTINOGENESIS IMPERFECTA AND IN ASSOCIATION WITH OSTEOGENESIS IMPERFECTA – A LITERATURE REVIEW

by Andrei Kozma, Doriana Agop Forna, Viorica Radoi, Ana Maria Alexandra Stanescu, Radu Ursu, Laurentiu Camil Bohaltea
Published 2018-12-01

HUMAN HEREDITARY ENAMELABNORMALITIES – MOLECULAR FACTORS AND GENETIC COUNSELLING

by Andrei Kozma, Doriana Agop Forna, Viorica Radoi, Radu Ursu, Agnes Katalin Lackner, Laurentiu Camil Bohiltea, Horia Lazarescu
Published 2019-06-01

DIFFERENTIAL DIAGNOSIS AND GENETIC TESTING FOR DETERMINING THE MOLECULAR CAUSES UNDERLYING ORO-DENTAL ANOMALIES IN A SERIES OF PATIENTS

by Viorica Radoi, Andrei Kozma, Vasilica Toma, Horia Lăzărescu, Radu Ursu, Agnes Katherine Lackner, Laurențiu Camil Bohîlțea, Norina Forna
Published 2019-07-01

Rare presentation and wide intrafamilial variability of Fabry disease: A case report and review of the literature

by Sebastian Militaru, Robert Adam, Lucian Dorobantu, Paolo Ferrazzi, Maria Iascone, Viorica Radoi, Gener Ismail, Bogdan A. Popescu, Ruxandra Jurcut
Published 2019-08-01

Novel FHL1 mutation variant identified in a patient with nonobstructive hypertrophic cardiomyopathy and myopathy – a case report

by Adrian Giucă, Cristina Mitu, Bogdan Ovidiu Popescu, Alexandra Eugenia Bastian, Răzvan Capşa, Adriana Mursă, Viorica Rădoi, Bogdan Alexandru Popescu, Ruxandra Jurcuţ
Published 2020-09-01