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Maedica
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August 27, 2024
Single Center Experience of Genetic Testing in Patients Undergoing Breast Cancer Treatment
Laura Mihaela Mustata, Gheorghe Peltecu, Diana Cezara Mugescu, et al.
Diagnostics (Basel, Switzerland)
|
November 26, 2022
Microduplication 3p26.3p24.3 and 4q34.3q35.2 Microdeletion Identified in a Patient with Developmental Delay Associated with Brain Malformation
Georgeta Cardos, Nicolae Gica, Corina Gica, et al.
Eye Science
|
May 28, 2015
Utilization of gene mapping and candidate gene mutation screening for diagnosing clinically equivocal conditions: a Norrie disease case study
Vasiliki Chini, Danai Stambouli, Florina Mihaela Nedelea, et al.
International Journal of Molecular Sciences
|
June 13, 2025
Challenges in Prenatal Ultrasound Diagnosis of Rubinstein-Taybi Syndrome: A Case Report and Comprehensive Literature Review
Daniela Roxana Matasariu, Iuliana-Elena Bujor, Roxana Maria Gireada, et al.
Children (Basel, Switzerland)
|
March 28, 2024
Prenatal Features of MIRAGE Syndrome-Case Report and Review of the Literature
Anca Maria Panaitescu, Iulia Huluță, Gabriel-Petre Gorecki, et al.
Medicina (Kaunas, Lithuania)
|
April 27, 2024
Beyond Weight Loss: A Comprehensive Review of Pregnancy Management following Bariatric Procedures
Iulia Huluță, Livia-Mihaela Apostol, Radu Botezatu, et al.
Reports (MDPI)
|
July 29, 2025
Amnion Rupture Sequence
Nicolae Gică, Florina Mihaela Nedelea, Livia Mihaela Apostol, et al.
Journal of Clinical Medicine
|
January 25, 2025
Maternal and Fetal Complications in Pregnant Women with Neurofibromatosis Type 1: Literature Review and Two Case Reports
Ancuta Nastac, Anca Maria Panaitescu, Iulia Huluță, et al.
Audiology Research
|
June 26, 2024
Congenital Cytomegalovirus-Related Hearing Loss
Nicoleta Gana, Iulia Huluță, Mihai-Ștefan Cătănescu, et al.
Romanian Journal of Morphology and Embryology = Revue Roumaine De Morphologie Et Embryologie
|
April 5, 2021
Case report of a novel phenotype in 18q deletion syndrome
Roxana Elena Bohîlţea, Monica Mihaela Cîrstoiu, Florina Mihaela Nedelea, et al.
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Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Maedica
|
August 27, 2024
Single Center Experience of Genetic Testing in Patients Undergoing Breast Cancer Treatment
Laura Mihaela Mustata, Gheorghe Peltecu, Diana Cezara Mugescu, et al.
Diagnostics (Basel, Switzerland)
|
November 26, 2022
Microduplication 3p26.3p24.3 and 4q34.3q35.2 Microdeletion Identified in a Patient with Developmental Delay Associated with Brain Malformation
Georgeta Cardos, Nicolae Gica, Corina Gica, et al.
Eye Science
|
May 28, 2015
Utilization of gene mapping and candidate gene mutation screening for diagnosing clinically equivocal conditions: a Norrie disease case study
Vasiliki Chini, Danai Stambouli, Florina Mihaela Nedelea, et al.
International Journal of Molecular Sciences
|
June 13, 2025
Challenges in Prenatal Ultrasound Diagnosis of Rubinstein-Taybi Syndrome: A Case Report and Comprehensive Literature Review
Daniela Roxana Matasariu, Iuliana-Elena Bujor, Roxana Maria Gireada, et al.
Children (Basel, Switzerland)
|
March 28, 2024
Prenatal Features of MIRAGE Syndrome-Case Report and Review of the Literature
Anca Maria Panaitescu, Iulia Huluță, Gabriel-Petre Gorecki, et al.
Medicina (Kaunas, Lithuania)
|
April 27, 2024
Beyond Weight Loss: A Comprehensive Review of Pregnancy Management following Bariatric Procedures
Iulia Huluță, Livia-Mihaela Apostol, Radu Botezatu, et al.
Reports (MDPI)
|
July 29, 2025
Amnion Rupture Sequence
Nicolae Gică, Florina Mihaela Nedelea, Livia Mihaela Apostol, et al.
Journal of Clinical Medicine
|
January 25, 2025
Maternal and Fetal Complications in Pregnant Women with Neurofibromatosis Type 1: Literature Review and Two Case Reports
Ancuta Nastac, Anca Maria Panaitescu, Iulia Huluță, et al.
Audiology Research
|
June 26, 2024
Congenital Cytomegalovirus-Related Hearing Loss
Nicoleta Gana, Iulia Huluță, Mihai-Ștefan Cătănescu, et al.
Romanian Journal of Morphology and Embryology = Revue Roumaine De Morphologie Et Embryologie
|
April 5, 2021
Case report of a novel phenotype in 18q deletion syndrome
Roxana Elena Bohîlţea, Monica Mihaela Cîrstoiu, Florina Mihaela Nedelea, et al.
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of 1