Genomics and Epigenomics in the Molecular Biology of Melanoma-A Prerequisite for Biomarkers Studies von Zob, Daniela Luminita, Augustin, Iolanda, Caba, Lavinia, Panzaru, Monica-Cristina, Popa, Setalia, Popa, Alina Delia, Florea, Laura, Gorduza, Eusebiu Vlad

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Cancer Predisposition Syndromes and Thyroid Cancer: Keys for a Short Two-Way Street von Balinisteanu, Ioana, Panzaru, Monica-Cristina, Caba, Lavinia, Ungureanu, Maria-Christina, Florea, Andreea, Grigore, Ana Maria, Gorduza, Eusebiu Vlad

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Genetic heterogeneity in corpus callosum agenesis von Pânzaru, Monica-Cristina, Popa, Setalia, Lupu, Ancuta, Gavrilovici, Cristina, Lupu, Vasile Valeriu, Gorduza, Eusebiu Vlad

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

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The Importance of Molecular Genetic Testing for Precision Diagnostics, Management, and Genetic Counseling in MODY Patients von Butnariu, Lăcrămioara Ionela, Bizim, Delia Andreia, Oltean, Carmen, Rusu, Cristina, Pânzaru, Monica Cristina, Păduraru, Gabriela, Gimiga, Nicoleta, Ghiga, Gabriela, Moisă, Ștefana Maria, Țarcă, Elena, Starcea, Iuliana Magdalena, Popa, Setalia, Trandafir, Laura Mihaela

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Epidermolysis Bullosa—A Different Genetic Approach in Correlation with Genetic Heterogeneity von Pânzaru, Monica-Cristina, Caba, Lavinia, Florea, Laura, Braha, Elena Emanuela, Gorduza, Eusebiu Vlad

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Genotype-Phenotype Correlations in 2q37-Deletion Syndrome: An Update of the Clinical Spectrum and Literature Review von Gavril, Eva-Cristiana, Nucă, Irina, Pânzaru, Monica-Cristina, Ivanov, Anca Viorica, Mihai, Cosmin-Teodor, Antoci, Lucian-Mihai, Ciobanu, Cristian-Gabriel, Rusu, Cristina, Popescu, Roxana

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Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11.2 Deletion Syndrome: Genotype–Phenotype Correlation von Gavril, Eva-Cristiana, Popescu, Roxana, Nucă, Irina, Ciobanu, Cristian-Gabriel, Butnariu, Lăcrămioara Ionela, Rusu, Cristina, Pânzaru, Monica-Cristina

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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 von 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

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

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

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

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Classification of osteogenesis imperfecta: Importance for prophylaxis and genetic counseling von Panzaru, Monica-Cristina, Florea, Andreea, Caba, Lavinia, Gorduza, Eusebiu Vlad

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

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

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

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

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ORPHAcodes use for the coding of rare diseases: comparison of the accuracy and cross country comparability von Mazzucato, Monica, Pozza, Laura Visonà Dalla, Facchin, Paola, Angin, Cèline, Agius, Francis, Cavero-Carbonell, Clara, Corrochano, Virginia, Hanusova, Katerina, Kirch, Kurt, Lambert, Deborah, Lucano, Caterina, Maiella, Sylvie, Panzaru, Monica, Rusu, Cristina, Weber, Stefanie, Zurriaga, Oscar, Zvolsky, Miroslav, Rath, Ana

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Genetic Features of mcr-1 Mediated Colistin Resistance in CMY-2-Producing Escherichia coli From Romanian Poultry von Maciuca, Iuliana E., Cummins, Max L., Cozma, Andreea P., Rimbu, Cristina M., Guguianu, Eleonora, Panzaru, Carmen, Licker, Monica, Szekely, Edit, Flonta, Mirela, Djordjevic, Steven P., Timofte, Dorina

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Clinical Aspects of a Rare Disease: Bardet Biedl Syndrome von FOCSA, Ina Ofelia, BUDISTEANU, Magdalena, STOICA, Cristina, NEDELEA, Florina, JURCA, Claudia, CABA, Lavinia, PANZARU, Monica, RUSU, Cristina, BALGRADEAN, Mihaela, BUTNARIU, Lacramioara

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