Maria Cristina Inserra, Alessia Di Mari, Giulia Passaniti, Maria Teresa Cannizzaro, Giuliana La Rosa, Daniela Poli, Placido Gitto, Laura Patanè, Placido Romeo. Imaging in a Rare Case of Neonatal Arterial Tortuosity Syndrome.Global medical genetics. 2023, 10 (4): 271-277
Maha Alotaibi, Amal Alqasmi, Faisal Albassam, Turki Alkahtani, Muath Alqahtany, Mohammed Alkhaldi. The First Reported Case of a Child with Two Different Rare Metabolic Disorders: Very Long-Chain Acyl-CoA Dehydrogenase Deficiency and Encephalomyopathic Mitochondrial DNA Depletion Syndrome 13.Global medical genetics. 2023, 10 (4): 278-281
Jiaying Liu, Lei Zhang. Primary Immune Thrombocytopenia in Pregnancy: Pathology, Diagnosis, and Management.Global medical genetics. 2023, 10 (4): 282-284
Ban Wang, Jichun Pan, Zhonghui Liu. Unraveling FOXO3a and USP18 Functions in Idiopathic Pulmonary Fibrosis through Single-Cell RNA Sequencing of Mouse and Human Lungs.Global medical genetics. 2023, 10 (4): 301-310
Athanasios Michas, Vasileios Michas, Evangelos Anagnostou, Michail Galanopoulos, Maria Tolia, Nikolaos Tsoukalas. The Clinical Significance of MicroRNAs in Colorectal Cancer Signaling Pathways: A Review.Global medical genetics. 2023, 10 (4): 315-323
Erum Khan, Soura Chakrabarty, Sanobar Shariff, Mainak Bardhan. Genetics and Genomics of Chronic Pancreatitis with a Focus on Disease Biology and Molecular Pathogenesis.Global medical genetics. 2023, 10 (4): 324-334
A Di Nora, M C Consentino, G Messina, T Timpanaro, P Smilari, P Pavone. Severe Hypernatremia as Presentation of Netherton Syndrome.Global medical genetics. 2023, 10 (4): 335-338
A Di Nora, G Pellino, A Di Mari, F Scarlata, F Greco, P Pavone. Early is Better: Report of a Cowden Syndrome.Global medical genetics. 2023, 10 (4): 345-347
Xin Qiu, Qing-Qing Jiang, Wei-Wei Guo, Ning Yu, Shi-Ming Yang. Study on Screening Core Biomarkers of Noise and Drug-Induced Hearing Loss Based on Transcriptomics.Global medical genetics. 2023, 10 (4): 357-369
Piero Pavone, Xena Giada Pappalardo, Claudia Parano, Enrico Parano, Antonio Corsello, Martino Ruggieri, Giovanni Cacciaguerra, Raffaele Falsaperla. Severe Unilateral Microtia with Aural Atresia, Hair White Patch, Stereotypes in a Young Boy with De novo 16p13.11 Deletion: Reasons for a New Genotype-Phenotype Correlation.Global medical genetics. 2023, 10 (4): 370-375
Polyanna Oliveira, Paula Correa, Angelina Acosta, Juliana Freitas, Taísa Machado-Lopes, Thais Bomfim-Palma, Ândrea Ribeiro-Dos-Santos, Sidney Santos, Roberto Nascimento, Ivana Nascimento, Kiyoko Abe-Sandes. Screening for Mutations in Hereditary Cancer Susceptibility Genes in a Region with High Endogamy in Brazil.Global medical genetics. 2023, 10 (4): 376-381