Classification of osteogenesis imperfecta: Importance for prophylaxis and genetic counseling

por Panzaru, Monica-Cristina, Florea, Andreea, Caba, Lavinia, Gorduza, Eusebiu Vlad
Publicado 2023

Epidermolysis Bullosa—A Different Genetic Approach in Correlation with Genetic Heterogeneity

por Pânzaru, Monica-Cristina, Caba, Lavinia, Florea, Laura, Braha, Elena Emanuela, Gorduza, Eusebiu Vlad
Publicado 2022

Genetic heterogeneity in corpus callosum agenesis

por Pânzaru, Monica-Cristina, Popa, Setalia, Lupu, Ancuta, Gavrilovici, Cristina, Lupu, Vasile Valeriu, Gorduza, Eusebiu Vlad
Publicado 2022

Cancer Predisposition Syndromes and Thyroid Cancer: Keys for a Short Two-Way Street

por Balinisteanu, Ioana, Panzaru, Monica-Cristina, Caba, Lavinia, Ungureanu, Maria-Christina, Florea, Andreea, Grigore, Ana Maria, Gorduza, Eusebiu Vlad
Publicado 2023

Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype–Phenotype Correlation

por Gavril, Eva-Cristiana, Popescu, Roxana, Nucă, Irina, Ciobanu, Cristian-Gabriel, Butnariu, Lăcrămioara Ionela, Rusu, Cristina, Pânzaru, Monica-Cristina
Publicado 2022

Genomics and Epigenomics in the Molecular Biology of Melanoma—A Prerequisite for Biomarkers Studies

por Zob, Daniela Luminita, Augustin, Iolanda, Caba, Lavinia, Panzaru, Monica-Cristina, Popa, Setalia, Popa, Alina Delia, Florea, Laura, Gorduza, Eusebiu Vlad
Publicado 2022

Genotype–Phenotype Correlations in 2q37-Deletion Syndrome: An Update of the Clinical Spectrum and Literature Review

por Gavril, Eva-Cristiana, Nucă, Irina, Pânzaru, Monica-Cristina, Ivanov, Anca Viorica, Mihai, Cosmin-Teodor, Antoci, Lucian-Mihai, Ciobanu, Cristian-Gabriel, Rusu, Cristina, Popescu, Roxana
Publicado 2023

Narrative Review: Update on the Molecular Diagnosis of Fragile X Syndrome

por Ciobanu, Cristian-Gabriel, Nucă, Irina, Popescu, Roxana, Antoci, Lucian-Mihai, Caba, Lavinia, Ivanov, Anca Viorica, Cojocaru, Karina-Alexandra, Rusu, Cristina, Mihai, Cosmin-Teodor, Pânzaru, Monica-Cristina
Publicado 2023

Wolf-Hirschhorn Syndrome: Clinical and Genetic Study of 7 New Cases, and Mini Review

por Gavril, Eva-Cristiana, Luca, Alina Costina, Curpan, Alexandrina-Stefania, Popescu, Roxana, Resmerita, Irina, Panzaru, Monica Cristina, Butnariu, Lacramioara Ionela, Gorduza, Eusebiu Vlad, Gramescu, Mihaela, Rusu, Cristina
Publicado 2021

Genetics of Hearing Impairment in North-Eastern Romania—A Cost-Effective Improved Diagnosis and Literature Review

por Resmerita, Irina, Cozma, Romica Sebastian, Popescu, Roxana, Radulescu, Luminita Mihaela, Panzaru, Monica Cristina, Butnariu, Lacramioara Ionela, Caba, Lavinia, Ilie, Ovidiu-Dumitru, Gavril, Eva-Cristiana, Gorduza, Eusebiu Vlad, Rusu, Cristina
Publicado 2020

Pallister–Killian Syndrome versus Trisomy 12p—A Clinical Study of 5 New Cases and a Literature Review

por Arghir, Aurora, Popescu, Roxana, Resmerita, Irina, Budisteanu, Magdalena, Butnariu, Lacramioara Ionela, Gorduza, Eusebiu Vlad, Gramescu, Mihaela, Panzaru, Monica Cristina, Papuc, Sorina Mihaela, Sireteanu, Adriana, Tutulan-Cunita, Andreea, Rusu, Cristina
Publicado 2021

Novel Mutation in APC Gene Associated with Multiple Osteomas in a Family and Review of Genotype-Phenotype Correlations of Extracolonic Manifestations in Gardner Syndrome

por Antohi, Cristina, Haba, Danisia, Caba, Lavinia, Ciofu, Mihai Liviu, Drug, Vasile-Liviu, Bărboi, Oana-Bogdana, Dobrovăț, Bogdan Ionuț, Pânzaru, Monica-Cristina, Gorduza, Nicoleta Carmen, Lupu, Vasile Valeriu, Dimofte, Doina, Gug, Cristina, Gorduza, Eusebiu Vlad
Publicado 2021

Current Data and New Insights into the Genetic Factors of Atherogenic Dyslipidemia Associated with Metabolic Syndrome

por Butnariu, Lăcramioara Ionela, Gorduza, Eusebiu Vlad, Țarcă, Elena, Pânzaru, Monica-Cristina, Popa, Setalia, Stoleriu, Simona, Lupu, Vasile Valeriu, Lupu, Ancuta, Cojocaru, Elena, Trandafir, Laura Mihaela, Moisă, Ștefana Maria, Florea, Andreea, Stătescu, Laura, Bădescu, Minerva Codruța
Publicado 2023

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

por 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
Publicado 2021