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Cited by in CrossRef
For: Jiang N, Mao WY, Peng BX, Yang TY, Mao XR. Clinical manifestations of adult hereditary spherocytosis with novel SPTB gene mutations and hyperjaundice: A case report. World J Clin Cases 2023; 11(6): 1349-1355 [PMID: 36926142 DOI: 10.12998/wjcc.v11.i6.1349]
URL: https://www.wjgnet.com/2307-8960/full/v11/i6/1349.htm
Number Citing Articles
1
Sana Habibzadeh, Majid Einakchi, Mohammad Ebrahim Kalantari, Farnood Forouhar, Arefeh Ma'souminejad. The coincidence of beta‐thalassemia and hereditary spherocytosis: A case report and literature reviewClinical Case Reports 2024; 12(6) doi: 10.1002/ccr3.9080