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Frontiers in Genetics|December 1, 2025
Familial Xq27.1q28 duplication arising from a maternal interarm forward insertion of the X chromosome: a case reportXiang Li, Yuan-Mei Peng, Bo-Wen Luo, et al.
Frontiers in Genetics|December 1, 2025
Novel variant in PNPLA6 gene causes Oliver-McFarlane syndrome in a Chinese family: 13 years follow-upPanpan Xiao, Yonghua Gu, Xiaolong Qi, et al.
Frontiers in Genetics|December 12, 2025
Case Report: developmental delay and intellectual disability linked to a maternally inherited derivative chromosome 3 from a t(3;8) translocationAndrés León, Alex S Aguirre, Anna Lindstrand, et al.
Frontiers in Genetics|December 10, 2025
Circular RNAs at the crossroads of acute pancreatitis: bridging molecular mechanisms to diagnostic and therapeutic innovationsJing Chen, XiaoLing Chen, Fei He
Frontiers in Genetics|December 8, 2025
Benign mosaic chromosomal structural variants across generations: evidence for a developmental correction mechanism from clinical and computational modelsJiayu Ruan, Qinhao Song, Yue Hu, et al.
Frontiers in Genetics|June 19, 2025
Polymorphisms in circadian rhythm genes and the risk of differentiated thyroid cancerTakiy-Eddine Berrandou, Emilie Cordina-Duverger, Claire Mulot, et al.
Frontiers in Genetics|February 13, 2025
GOLPH3 inhibits glioma cell apoptosis through the JNK signaling pathwayShao Xie, Jiahai Ding, Zhaohao Wang, et al.
Frontiers in Genetics|February 13, 2025
Quadratic descriptors and reduction methods in a two-layered model for compound inferenceJianshen Zhu, Naveed Ahmed Azam, Shengjuan Cao, et al.
Frontiers in Genetics|February 12, 2025
Impacts of stem cells from different sources on wound healing rate in diabetic foot ulcers: a systematic review and meta-analysisLe Tong, Lin Tang, Bangli Tang, et al.
Frontiers in Genetics|February 12, 2025
Case report: Discovery of novel CTNNB1 mutations and comparison of clinical characteristics in two patients with NEDSDVEojin Lee, Ja Young Choi, Shin-Seung Yang
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