| Wolf-Hirschhorn Syndrome: Clinical and Genetic Study of 7 New Cases, and Mini Review EC Gavril, AC Luca, AS Curpan, R Popescu, I Resmerita, MC Panzaru, ... Children 8 (9), 751, 2021 | 18 | 2021 |
| Genetics of Hearing Impairment in North-Eastern Romania—A Cost-Effective Improved Diagnosis and Literature Review I Resmerita, RS Cozma, R Popescu, LM Radulescu, MC Panzaru, ... Genes 11 (12), 1506, 2020 | 15 | 2020 |
| Different Types of Deletions Created by Low-Copy Repeats Sequences Location in 22q11. 2 Deletion Syndrome: Genotype–Phenotype Correlation EC Gavril, R Popescu, I Nucă, CG Ciobanu, LI Butnariu, C Rusu, ... Genes 13 (11), 2083, 2022 | 4 | 2022 |
| Pallister–Killian Syndrome versus Trisomy 12p—A Clinical Study of 5 New Cases and a Literature Review A Arghir, R Popescu, I Resmerita, M Budisteanu, LI Butnariu, EV Gorduza, ... Genes 12 (6), 811, 2021 | 4 | 2021 |
| Genotype–Phenotype Correlations in 2q37-Deletion Syndrome: An Update of the Clinical Spectrum and Literature Review EC Gavril, I Nucă, MC Pânzaru, AV Ivanov, CT Mihai, LM Antoci, ... Genes 14 (2), 465, 2023 | 2 | 2023 |
| Narrative Review: Update on the Molecular Diagnosis of Fragile X Syndrome CG Ciobanu, I Nucă, R Popescu, LM Antoci, L Caba, AV Ivanov, ... International Journal of Molecular Sciences 24 (11), 9206, 2023 | 1 | 2023 |
| OCULO-AURICULO-VERTEBRAL SPECTRUM: CLINICAL FEATURES IN A COHORT OF 37 PATIENTS I RESMERIȚĂ, BM COBZEANU, P Setalia, EC GAVRIL, V MARTINIUC, ... The Medical-Surgical Journal 125 (4), 578-584, 2021 | | 2021 |
| 1p36 deletion syndrome-Iasi Regional Medical Genetics Centre's Experience C Rusu, R Popescu, M Panzaru, L Butnariu, I Resmerita, E Gavril EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 577-578, 2020 | | 2020 |
| Clinical & genetic characteristics of syndromes associated with craniosynostosis M Danila, M Tonu, M Panzaru, L Butnariu, R Popescu, C Banescu, ... EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 461-461, 2020 | | 2020 |
| Mutational analysis of the most frequent genes in Romanian patients with congenital non-syndromic hearing loss I Resmerita, S Cozma, M Panzaru, E Gorduza, R Popescu, L Radulescu, ... EUROPEAN JOURNAL OF HUMAN GENETICS 28 (SUPPL 1), 812-813, 2020 | | 2020 |
| Correlation between reason to apply a prenatal diagnosis for aneuploidy and the results of test-A retrospective study on 2,881 foetus investigated in last 15 years by FISH … V Martiniuc, M Gramescu, S Popa, R Popescu, A Paduret, I Resmerita, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1204-1204, 2019 | | 2019 |
| Miller-Dieker syndrome: different phenotypes in 5 cases E Gavril, R Popescu, M Panzaru, I Resmerita, C Rusu EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1881-1881, 2019 | | 2019 |
| Evolution in time and hearing impairment in oculo-auriculo-vertebral spectrum I Resmerita, S Cozma, R Popescu, E Gavril, L Butnariu, M Panzaru, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1883-1884, 2019 | | 2019 |
| Long-time follow-up and hearing impairment in four patients with Treacher Collins syndrome I Resmerita, S Cozma, R Popescu, M Panzaru, L Butnariu, C Rusu EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1006-1006, 2019 | | 2019 |
| Poland Sequence-long time follow-up of 21 cases GE Girnet, R Popescu, M Gramescu, I Resmerita, M Panzaru, L Butnariu, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 375-375, 2019 | | 2019 |
| Williams-Beuren syndrome: clinical variability in a Nord-Eastern Romanian cohort E Gavril, R Popescu, EV Gorduza, M Gramescu, I Resmerita, L Butnariu, ... EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1010-1010, 2019 | | 2019 |
| Rare cytogenetic anomalies in 2q37 microdeletion syndrome MC Panzaru, R Popescu, M Gramescu, L Butnariu, I Resmerita, C Rusu, ... MOLECULAR CYTOGENETICS 10, 2017 | | 2017 |
| A NEW CASE OF HEREDITARY GINGIVAL FIBROMATOSIS. L Caba, C Ungureanu, M Grămescu, M Pânzaru, L Butnariu, R Popescu, ... Romanian Journal of Functional & Clinical, Macro-& Microscopical Anatomy …, 2017 | | 2017 |
| Campomelic dysplasia with dextrocardia and without sex-reversal O Păvăloaia, I Resmeriţă, I Augustin, M Pânzaru, V Martiniuc, L Păduraru, ... Archive of Clinical Cases 4 (1), 2017 | | 2017 |
| PHENOTYPIC VARIABILITY IN EDWARDS SYNDROME: SYNOPSIS OF 19 CASES WITH TRISOMY 18 M Panzaru, C Lavinia, R Cristina, L Butnariu, E Braha, R Popescu, ... The Medical-Surgical Journal 121 (1), 172-177, 2017 | | 2017 |
Monica PanzaruUMF Grigore T Popa Iasi在 umfiasi.ro 的电子邮件经过验证
