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Oct 26, 2019 (publication date) through May 2, 2024
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Publication Name
World Journal of Clinical Cases
ISSN
2307-8960
Publisher of This Article
Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA
| For: | Li Y, Li Y, Yang Y, Yang WR, Li JP, Peng GX, Song L, Fan HH, Ye L, Xiong YZ, Wu ZJ, Zhou K, Zhao X, Jing LP, Zhang FK, Zhang L. Next generation sequencing reveals co-existence of hereditary spherocytosis and Dubin–Johnson syndrome in a Chinese gril: A case report. World J Clin Cases 2019; 7(20): 3303-3309 [PMID: 31667183 DOI: 10.12998/wjcc.v7.i20.3303] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v7/i20/3303.htm |
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Zhanhui Du, Gang Luo, Kuiliang Wang, Zhen Bing, Silin Pan. Identification of a novel heterozygous SPTB mutation by whole genome sequencing in a Chinese patient with hereditary spherocytosis and atrial septal defect: a case report. BMC Pediatrics 2021; 21(1) doi: 10.1186/s12887-021-02771-4
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Astrid J Rodriguez-Acevedo, Louisa G Gordon, Nicola Waddell, Georgina Hollway, Lata Vadlamudi. Developing a gene panel for pharmacoresistant epilepsy: a review of epilepsy pharmacogenetics. Pharmacogenomics 2021; 22(4): 225 doi: 10.2217/pgs-2020-0145
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Haiyan Fu, Ruiqin Zhao, Xiaoyun Jia, Xiaolei Li, Guigui Li, Chunlan Yin. Neonatal Dubin–Johnson syndrome: biochemical parameters, characteristics, and genetic variants study. Pediatric Research 2021; doi: 10.1038/s41390-021-01583-7
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