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Cited by in CrossRef
For: Huang TT, Xu HF, Wang SY, Lin WX, Tung YH, Khan KU, Zhang HH, Guo H, Zheng G, Zhang G. Identification of 1q21.1 microduplication in a family: A case report. World J Clin Cases 2023; 11(4): 874-882 [PMID: 36818619 DOI: 10.12998/wjcc.v11.i4.874]
URL: https://www.wjgnet.com/2307-8960/full/v11/i4/874.htm
Number Citing Articles
1
Behjat Ul Mudassir, Mashael Alhumaidi Alotaibi, Nadeem Kizilbash, Daliyah Alruwaili, Anwar Alruwaili, Modhi Alenezi, Zehra Agha. Genome-wide CNV analysis uncovers novel pathogenic regions in cohort of five multiplex families with neurodevelopmental disordersHeliyon 2023; 9(9): e19718 doi: 10.1016/j.heliyon.2023.e19718