| 736398 |
FRONTIERS IN GENETICS |
Case Report: Identification of a Novel Pathogenic Germline TP53 Variant in a Family With Li–Fraumeni Syndrome |
2021-09-01 |
10.3389/fgene.2021.734809 |
Paduano Francesco, Fabiani Fernanda, Colao Emma, Trapasso Francesco, Perrotti Nicola, Barbieri Vito, Baudi Francesco, Iuliano Rodolfo |
| 736397 |
FRONTIERS IN GENETICS |
Association of Genetic Variants With Body-Mass Index and Blood Pressure in Adolescents: A Replication Study |
2021-09-01 |
10.3389/fgene.2021.690335 |
Goulet Danick, O’Loughlin Jennifer, Sylvestre Marie-Pierre |
| 736396 |
FRONTIERS IN GENETICS |
DNA Double-Strand Break Repair: All Roads Lead to HeterochROMAtin Marks |
2021-09-01 |
10.3389/fgene.2021.730696 |
Caron Pierre, Pobega Enrico, Polo Sophie E. |
| 736395 |
FRONTIERS IN GENETICS |
Case Report: Second Report of Joubert Syndrome Caused by Biallelic Variants in IFT74 |
2021-09-01 |
10.3389/fgene.2021.738157 |
Zhongling Ke, Guoming Li, Yanhui Chen, Xiaoru Chen |
| 736394 |
FRONTIERS IN GENETICS |
Physical and Functional Interaction of Mitochondrial Single-Stranded DNA-Binding Protein and the Catalytic Subunit of DNA Polymerase Gamma |
2021-09-01 |
10.3389/fgene.2021.721864 |
Ciesielski Grzegorz L., Kim Shalom, de Bovi Pontes Carolina, Kaguni Laurie S. |
| 736393 |
FRONTIERS IN GENETICS |
Case Report: Two New Cases of Chromosome 12q14 Deletions and Review of the Literature |
2021-09-01 |
10.3389/fgene.2021.716874 |
Deng Ruizhi, McCalman Melysia T., Bossuyt Thomas P., Barakat Tahsin Stefan |
| 736392 |
FRONTIERS IN GENETICS |
Editorial: Epigenetic Mechanisms and Their Involvement in Rare Diseases |
2021-09-01 |
10.3389/fgene.2021.755076 |
Rastegar Mojgan, Yasui Dag H. |
| 736391 |
FRONTIERS IN GENETICS |
A Nomogram Integrating Ferroptosis- and Immune-Related Biomarkers for Prediction of Overall Survival in Lung Adenocarcinoma |
2021-09-01 |
10.3389/fgene.2021.706814 |
Chai Mengyu, Li Xiuchun, Zhang Yaxin, Tang Yemeng, Shu Pingping, Lin Jing, Shi Keqing, Wang Liangxing, Huang Xiaoying |
| 736390 |
FRONTIERS IN GENETICS |
Clinical Application of Whole Exome Sequencing for Monogenic Disorders in PICU of China |
2021-09-01 |
10.3389/fgene.2021.677699 |
Liu Yingchao, Hao Chanjuan, Li Kechun, Hu Xuyun, Gao Hengmiao, Zeng Jiansheng, Guo Ruolan, Liu Jun, Guo Jun, Li Zheng, Qi Zhan, Jia Xinlei, Li Wei, Qian Suyun |
| 736389 |
FRONTIERS IN GENETICS |
Characterization of the Potential Role of NTPCR in Epithelial Ovarian Cancer by Integrating Transcriptomic and Metabolomic Analysis |
2021-09-01 |
10.3389/fgene.2021.695245 |
Shang Hongkai, Zhang Huizhi, Ren Ziyao, Zhao Hongjiang, Zhang Zhifen, Tong Jinyi |
