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Lavinia Caba

Showing results (21-30 of 34) with videos related to

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Revista Medico-Chirurgicala a Societatii De Medici Si Naturalisti Din Iasi|April 19, 2011
[Idiopathic mental retardation--importance of clinical diagnostic scores for case selection]Lavinia Caba, Cristina Rusu, M Voloşciuc, et al.
Revista Medico-Chirurgicala a Societatii De Medici Si Naturalisti Din Iasi|February 8, 2014
Genotype- phenotype correlation in trisomy X: a retrospective study of a selected group of 36 patients and review of literatureLăcrămioara Butnariu, Cristina Rusu, Lavinia Caba, et al.
International Journal of Molecular Sciences|January 8, 2023
Genomics and Epigenomics in the Molecular Biology of Melanoma-A Prerequisite for Biomarkers StudiesDaniela Luminita Zob, Iolanda Augustin, Lavinia Caba, et al.
Current Issues in Molecular Biology|August 28, 2024
Unlocking the Genetic Secrets of Acromegaly: Exploring the Role of Genetics in a Rare DisorderIoana Balinisteanu, Lavinia Caba, Andreea Florea, et al.
Genes|September 27, 2025
Genetic and Epigenetic Factors in Ulcerative Colitis: A Narrative Literature ReviewLavinia Caba, Andreea Florea, Petru Cianga, et al.
Revista Medico-Chirurgicala a Societatii De Medici Si Naturalisti Din Iasi|December 18, 2013
Prenatal diagnosis of gonosomal anomalies: limitations of the FISH method and genetic counseling difficulties in 15 casesElena Braha, Violeta Martiniuc, Monica Panzaru, et al.
Revista Medico-Chirurgicala a Societatii De Medici Si Naturalisti Din Iasi|December 18, 2013
Phenotypic variability in Patau syndromeLavinia Caba, Cristina Rusu, Lacramioara Butnariu, et al.
Medicina (Kaunas, Lithuania)|January 21, 2022
Genetic Counseling and Management: The First Study to Report NIPT Findings in a Romanian PopulationCristina Gug, Ioana Mozos, Adrian Ratiu, et al.
International Journal of Molecular Sciences|June 10, 2023
Narrative Review: Update on the Molecular Diagnosis of Fragile X SyndromeCristian-Gabriel Ciobanu, Irina Nucă, Roxana Popescu, et al.
Revista Medico-Chirurgicala a Societatii De Medici Si Naturalisti Din Iasi|November 4, 2011
[Improvement of genetic diagnostic strategy in velo-cardio-facial syndrome]Monica Pânzaru, Cristina Rusu, M Voloşciuc, et al.
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Showing results (21-30 of 34) with videos related to

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Pageof 4
Revista Medico-Chirurgicala a Societatii De Medici Si Naturalisti Din Iasi|April 19, 2011
[Idiopathic mental retardation--importance of clinical diagnostic scores for case selection]Lavinia Caba, Cristina Rusu, M Voloşciuc, et al.
Revista Medico-Chirurgicala a Societatii De Medici Si Naturalisti Din Iasi|February 8, 2014
Genotype- phenotype correlation in trisomy X: a retrospective study of a selected group of 36 patients and review of literatureLăcrămioara Butnariu, Cristina Rusu, Lavinia Caba, et al.
International Journal of Molecular Sciences|January 8, 2023
Genomics and Epigenomics in the Molecular Biology of Melanoma-A Prerequisite for Biomarkers StudiesDaniela Luminita Zob, Iolanda Augustin, Lavinia Caba, et al.
Current Issues in Molecular Biology|August 28, 2024
Unlocking the Genetic Secrets of Acromegaly: Exploring the Role of Genetics in a Rare DisorderIoana Balinisteanu, Lavinia Caba, Andreea Florea, et al.
Genes|September 27, 2025
Genetic and Epigenetic Factors in Ulcerative Colitis: A Narrative Literature ReviewLavinia Caba, Andreea Florea, Petru Cianga, et al.
Revista Medico-Chirurgicala a Societatii De Medici Si Naturalisti Din Iasi|December 18, 2013
Prenatal diagnosis of gonosomal anomalies: limitations of the FISH method and genetic counseling difficulties in 15 casesElena Braha, Violeta Martiniuc, Monica Panzaru, et al.
Revista Medico-Chirurgicala a Societatii De Medici Si Naturalisti Din Iasi|December 18, 2013
Phenotypic variability in Patau syndromeLavinia Caba, Cristina Rusu, Lacramioara Butnariu, et al.
Medicina (Kaunas, Lithuania)|January 21, 2022
Genetic Counseling and Management: The First Study to Report NIPT Findings in a Romanian PopulationCristina Gug, Ioana Mozos, Adrian Ratiu, et al.
International Journal of Molecular Sciences|June 10, 2023
Narrative Review: Update on the Molecular Diagnosis of Fragile X SyndromeCristian-Gabriel Ciobanu, Irina Nucă, Roxana Popescu, et al.
Revista Medico-Chirurgicala a Societatii De Medici Si Naturalisti Din Iasi|November 4, 2011
[Improvement of genetic diagnostic strategy in velo-cardio-facial syndrome]Monica Pânzaru, Cristina Rusu, M Voloşciuc, et al.
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