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For: Guo X, Liu K, Liu Y, Situ Y, Tian X, Xu KF, Zhang X. Clinical and genetic characteristics of cystic fibrosis in CHINESE patients: a systemic review of reported cases. Orphanet J Rare Dis 2018;13:224. [PMID: 30558651 DOI: 10.1186/s13023-018-0968-2] [Cited by in Crossref: 19] [Cited by in F6Publishing: 21] [Article Influence: 4.8] [Reference Citation Analysis]
Number Citing Articles
1 Fang J, Wang X, Sun X, Cui Y, Diao F, Yang X. Congenital absence of the vas deferens with hypospadias or without hypospadias: Phenotypic findings and genetic considerations. Front Genet 2022;13. [DOI: 10.3389/fgene.2022.1035468] [Reference Citation Analysis]
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4 Nabavizadeh H, Johari L, Noeiaghdam R, Alyasin S, Esmaeilzadeh H, Kanannejad Z, Emaminia M. An unusual case of cystic fibrosis with pancytopenia due to copper deficiency and blindness caused by vitamin A deficiency: A case-report. Respiratory Medicine Case Reports 2022;40:101774. [DOI: 10.1016/j.rmcr.2022.101774] [Reference Citation Analysis]
5 Chen HH, Lin CH, Chao WC. Mortality association of nontuberculous mycobacterial infection requiring treatment in Taiwan: a population-based study. Ther Adv Respir Dis 2022;16:17534666221103213. [PMID: 35748569 DOI: 10.1177/17534666221103213] [Reference Citation Analysis]
6 Zeng Y, Xue X, Cai H, Zhu G, Zhu M, Wang J, Song X, Mo Y, Gao X, Zhou J, Ye L, Jin M. Clinical Characteristics and Prognosis of Allergic Bronchopulmonary Aspergillosis: A Retrospective Cohort Study. JAA 2022;Volume 15:53-62. [DOI: 10.2147/jaa.s345427] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 He M, Xie H, Du L, Lei T, Zhang L. Postnatal outcomes of fetuses with isolated gallbladder anomalies: be aware of biliary atresia. J Matern Fetal Neonatal Med 2021;:1-6. [PMID: 34470134 DOI: 10.1080/14767058.2021.1933936] [Reference Citation Analysis]
8 Yang B, Lei C, Yang D, Tan Z, Guo T, Luo H. Whole-Exome Sequencing Identified CFTR Variants in Two Consanguineous Families in China. Front Genet 2021;12:631221. [PMID: 34276759 DOI: 10.3389/fgene.2021.631221] [Reference Citation Analysis]
9 Alghamdi SS, Alhamyani NM, Alamri HM, Alzahrani TS, Daghas SM, Bakri RH, Basehi AF, Almarashi AS, Alrajehi AM, Al Ghanim DZ. Latest Advances in Gene Therapy in Management of Cystic Fibrosis Lung Disease, Literature Review. J Biochem Technol 2021;12:67-70. [DOI: 10.51847/usni3jothd] [Reference Citation Analysis]
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11 Shen Y, Tang X, Liu J, Li H, Zhao S. Pseudo‐Bartter syndrome in Chinese children with cystic fibrosis: Clinical features and genotypic findings. Pediatr Pulmonol 2020;55:3021-9. [DOI: 10.1002/ppul.25012] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
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15 Nappo S, Mannucci L, Novelli G, Sangiuolo F, D'Apice MR, Botta A. Carrier frequency of CFTR variants in the non-Caucasian populations by genome aggregation database (gnomAD)-based analysis. Ann Hum Genet 2020;84:463-8. [PMID: 32484936 DOI: 10.1111/ahg.12396] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 2.0] [Reference Citation Analysis]
16 Shao H, Hua J, Wu Q, Li X, Zhang M, Wang H, Wu J, Xu L, Xie Y, Li L, Chen H. Identification of a Mutation in the Novel Compound Heterozygous CFTR in a Chinese Family with Cystic Fibrosis. Can Respir J 2020;2020:6507583. [PMID: 32454915 DOI: 10.1155/2020/6507583] [Reference Citation Analysis]
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18 Bittles A. Precision medicine: Rare diseases and community genetics. Digit Med 2019;5:154. [DOI: 10.4103/digm.digm_29_19] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]