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Liu Xinyu, He Rugu, Cui Qingyang.
Clinical phenotypic characteristics and gene mutation spectrum analysis of inherited metabolic diseases in neonates presenting with gastrointestinal symptoms
[J]. Clinical Focus, 2026, 41(5): 429-440.
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Zhang Yifan, Wang Ning, Song Zhan, Xu Ensong.
Clinicopathological characteristics and KRAS/NRAS/BRAF mutation profiles by microsatellite instability status in colorectal cancer
[J]. Clinical Focus, 2026, 41(2): 135-139.
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Zhao Wei, Xu Huijuan, Zhao Yanxia, Wang Lingzhen, Lu Yuan, Yang Jing.
Malignant osteopetrosis in infants: A case report and literature review
[J]. Clinical Focus, 2025, 40(8): 726-730.
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Zhang Hui, Zhang Wenbo, Liang Wenqi, Huo Yanhong.
Idiopathic renal hypouricemia combined with repeated acute kidney injury: A case report and literature review
[J]. Clinical Focus, 2025, 40(2): 168-171.
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Zhang Wenxiao, Wang Wenhong.
CUBN variants in child with isolated proteinuria: A case report and literature review
[J]. Clinical Focus, 2025, 40(10): 930-934.
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Lv Shasha, Song Jinlan, Shi Jian.
Mitochondrial mutation m.3243A> G associated with diabetes mellitus: One case report and literature review
[J]. Clinical Focus, 2024, 39(2): 160-163.
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Cui Qingyang, Wang Mengbin, Cao Yinli, Tang Chenghe.
A case report and literature review on severe combined immunodeficiency caused by new mutation of RAG1 gene
[J]. Clinical Focus, 2022, 37(2): 155-161.
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Qin Yazhen.
Standardized detection of BCR-ABL mRNA and clinical application in patients with chronic myeloid leukemia
[J]. Clinical Focus, 2021, 36(10): 884-888.
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Chen Xingxing, Lei Xiaoyan, Sun Yonghong, Hu Xiaoxia, Zhao Shuzhen .
[J]. Clinical Focus, 2020, 35(11): 1019-1025.
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Feng Sanli1,2, Zhang Jingnan2, Qiao Shukai2, Wang Wenfei1, Li Yang2, Xing Lina2, Guo Xiaonan2.
Primary myelofibrosis with paroxysmal nocturnal hemoglobinuria: a case report and literature review
[J]. Clinical Focus, 2019, 34(12): 1119-1122.
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Wang Weia， Jiang Jianga， Rong Guanga， Huang Honga， Zhang Yongshengb， Shi Yizhena.
Epidermal growth factor receptor mutations in nonsmall cell lung cancer and clinical background
[J]. Clinical Focus, 2017, 32(11): 957-960.
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Han Ying.
State and advance of familial colorectal cancer without identifiable gene mutations
[J]. Clinical Focus, 2016, 31(6): 585-589.
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Pi Yalei， Zhang Yanan， Han Xiao， Men Xinyi， Li Chaonan， Zhang Huifeng.
Clinical and pedigree analysis of one child with autoimmune polyendocrinopathy syndrome typeⅠ caused by rare gene mutation
[J]. Clinical Focus, 2016, 31(12): 1318-1320.
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Hao Jianling;Zou Yue.
Relationship between ethambutol-resistance and mutations in embB306 gene of mycobacterium tuberculosis in Qingdao area
[J]. Clinical Focus, 2015, 30(1): 41-4347.
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YAN Na-xin;HUO Jian-feng;LU Fei;DU Jing;LI Tie-niu;ZHAO Zhao-xia;DAI Er-hei.
Analysis on L-nucleoside antiviral drug resistance mutation in Shijiazhuang region
[J]. Clinical Focus, 2014, 29(10): 1175-1177.
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