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Aurora Arghir

Showing results (11-20 of 26) with videos related to

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Journal of Child Neurology|February 1, 2012
3p interstitial deletion: novel case report and reviewAndreea Cristina Ţuţulan-Cunită, Sorina Mihaela Papuc, Aurora Arghir, et al.
Psychiatry Research|February 28, 2012
Atypical presentations of 22q11.2 deletion syndrome: explaining the genetic defects and genome architectureAndreea Cristina Tuţulan-Cuniţă, Magdalena Budişteanu, Sorina Mihaela Papuc, et al.
European Journal of Medical Genetics|April 11, 2015
Microduplications of 3p26.3p26.2 containing CRBN gene in patients with intellectual disability and behavior abnormalitiesSorina M Papuc, Karl Hackmann, Joris Andrieux, et al.
Maedica|May 3, 2014
Diagnostic approach of angelman syndromeDenis George Duca, Dana Craiu, Monica Boer, et al.
Clinical Case Reports|January 28, 2021
Autism and severe clinical phenotype in a patient with 8p21.2p11.21 deletion: Case report and literature reviewAurora Arghir, Sorina Mihaela Papuc, Andreea-Cristina Tutulan-Cunita, et al.
Experimental and Therapeutic Medicine|January 3, 2022
Clinical and genomic findings in brain heterotopia: Report of a pediatric patient cohort from RomaniaMagdalena Budisteanu, Sorina Mihaela Papuc, Alina Erbescu, et al.
Genes|August 6, 2021
The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 PatientsMagdalena Budisteanu, Sorina Mihaela Papuc, Ioana Streata, et al.
Genes|June 2, 2021
Pallister-Killian Syndrome versus Trisomy 12p-A Clinical Study of 5 New Cases and a Literature ReviewAurora Arghir, Roxana Popescu, Irina Resmerita, et al.
Genes|August 28, 2025
<i>FMR1</i> Methylation Pattern and Repeat Expansion Screening in a Cohort of Boys with Autism Spectrum Disorders: Correlation of Genetic Findings with Clinical PresentationsMaria Dobre, Gisela Gaina, Alina Erbescu, et al.
Hematology Reports|December 27, 2024
Incorporation of a Comorbidity Index in Treatment Decisions for Elderly AML Patients Can Lead to Better Disease Management-A Single-Center ExperienceCristina Negotei, Iuliana Mitu, Silvana Angelescu, et al.
Pageof 3

Showing results (11-20 of 26) with videos related to

Sort By:
Pageof 3
Journal of Child Neurology|February 1, 2012
3p interstitial deletion: novel case report and reviewAndreea Cristina Ţuţulan-Cunită, Sorina Mihaela Papuc, Aurora Arghir, et al.
Psychiatry Research|February 28, 2012
Atypical presentations of 22q11.2 deletion syndrome: explaining the genetic defects and genome architectureAndreea Cristina Tuţulan-Cuniţă, Magdalena Budişteanu, Sorina Mihaela Papuc, et al.
European Journal of Medical Genetics|April 11, 2015
Microduplications of 3p26.3p26.2 containing CRBN gene in patients with intellectual disability and behavior abnormalitiesSorina M Papuc, Karl Hackmann, Joris Andrieux, et al.
Maedica|May 3, 2014
Diagnostic approach of angelman syndromeDenis George Duca, Dana Craiu, Monica Boer, et al.
Clinical Case Reports|January 28, 2021
Autism and severe clinical phenotype in a patient with 8p21.2p11.21 deletion: Case report and literature reviewAurora Arghir, Sorina Mihaela Papuc, Andreea-Cristina Tutulan-Cunita, et al.
Experimental and Therapeutic Medicine|January 3, 2022
Clinical and genomic findings in brain heterotopia: Report of a pediatric patient cohort from RomaniaMagdalena Budisteanu, Sorina Mihaela Papuc, Alina Erbescu, et al.
Genes|August 6, 2021
The Phenotypic Spectrum of 15q13.3 Region Duplications: Report of 5 PatientsMagdalena Budisteanu, Sorina Mihaela Papuc, Ioana Streata, et al.
Genes|June 2, 2021
Pallister-Killian Syndrome versus Trisomy 12p-A Clinical Study of 5 New Cases and a Literature ReviewAurora Arghir, Roxana Popescu, Irina Resmerita, et al.
Genes|August 28, 2025
<i>FMR1</i> Methylation Pattern and Repeat Expansion Screening in a Cohort of Boys with Autism Spectrum Disorders: Correlation of Genetic Findings with Clinical PresentationsMaria Dobre, Gisela Gaina, Alina Erbescu, et al.
Hematology Reports|December 27, 2024
Incorporation of a Comorbidity Index in Treatment Decisions for Elderly AML Patients Can Lead to Better Disease Management-A Single-Center ExperienceCristina Negotei, Iuliana Mitu, Silvana Angelescu, et al.
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