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Experimental and Therapeutic Medicine|December 28, 2020
Heterogeneity in combined immunodeficiencies with associated or syndromic features (Review)Lavinia Caba, Cristina Gug, Eusebiu Vlad GorduzaFrontiers in Pediatrics|June 20, 2022
Genetic Heterogeneity in Bartter Syndrome: Clinical and Practical ImportanceLaura Florea, Lavinia Caba, Eusebiu Vlad GorduzaGenes|September 28, 2021
Bardet-Biedl Syndrome-Multiple Kaleidoscope Images: Insight into Mechanisms of Genotype-Phenotype CorrelationsLaura Florea, Lavinia Caba, Eusebiu Vlad GorduzaChildren (Basel, Switzerland)|February 24, 2024
Rare Case of First Permanent Molar Primary Failure of Eruption with Agenesis of PremolarsArina Vinereanu, Aneta Munteanu, Francois Clauss, et al.World Journal of Clinical Cases|May 22, 2023
Classification of osteogenesis imperfecta: Importance for prophylaxis and genetic counselingMonica-Cristina Panzaru, Andreea Florea, Lavinia Caba, et al.Biomolecules|December 24, 2021
Circular RNA-Is the Circle Perfect?Lavinia Caba, Laura Florea, Cristina Gug, et al.Diagnostics (Basel, Switzerland)|June 24, 2022
Epidermolysis Bullosa-A Different Genetic Approach in Correlation with Genetic HeterogeneityMonica-Cristina Pânzaru, Lavinia Caba, Laura Florea, et al.Journal of Multidisciplinary Healthcare|October 4, 2022
Monitoring and Management of Bardet-Biedl Syndrome: What the Multi-Disciplinary Team Can DoLavinia Caba, Laura Florea, Elena Emanuela Braha, et al.Frontiers in Genetics|October 17, 2022
Genetic heterogeneity in corpus callosum agenesisMonica-Cristina Pânzaru, Setalia Popa, Ancuta Lupu, et al.Gene|March 14, 2020
Rare splicing mutation in COL1A1 gene identified by whole exomes sequencing in a patient with osteogenesis imperfecta type I followed by prenatal diagnosis: A case report and review of the literatureCristina Gug, Lavinia Caba, Ioana Mozos, et al.Pageof 4