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 disorders. Heliyon 2023; 9(9): e19718 doi: 10.1016/j.heliyon.2023.e19718
|