For: | Zhu YY, Sun GL, Yang ZL. SATB2-associated syndrome caused by a novel SATB2 mutation in a Chinese boy: A case report and literature review. World J Clin Cases 2021; 9(21): 6081-6090 [PMID: 34368330 DOI: 10.12998/wjcc.v9.i21.6081] |
---|---|
URL: | https://www.wjgnet.com/2307-8960/full/v9/i21/6081.htm |
Number | Citing Articles |
1 |
Nada Benyahya, Nada Amllal, Siham Chafai Elalaoui, Mustapha El Alloussi, Abdelaziz Sefiani, Jaber Lyahyai. Novel variant related to SATB2‐associated syndrome. International Journal of Developmental Neuroscience 2024; 84(8): 1006 doi: 10.1002/jdn.10379
|
2 |
S. E. Nagieva, N. A. Semenova, A. R. Morgul, Zh. G. Markova, T. I. Yanova, N. A. Vorobyov, O. S. Groznova, M. V. Vorontsova, N. A. Bodunova. Clinical and genetic heterogeneity of SATB2-associated syndrome. Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics) 2025; 69(6): 27 doi: 10.21508/1027-4065-2024-69-6-27-33
|