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Aug 16, 2021 (publication date) through Nov 26, 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: | Lin SZ, Zhou XY, Wang WQ, Jiang K. Autism with dysphasia accompanied by mental retardation caused by FOXP1 exon deletion: A case report. World J Clin Cases 2021; 9(23): 6858-6866 [PMID: 34447835 DOI: 10.12998/wjcc.v9.i23.6858] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v9/i23/6858.htm |
| Number | Citing Articles |
| 1 |
Ru Ba, Lin Yang, Baoshen Zhang, Pengfei Jiang, Zhipeng Ding, Xue Zhou, Zhengang Yang, Chunjie Zhao. FOXG1 drives transcriptomic networks to specify principal neuron subtypes during the development of the medial pallium. Science Advances 2023; 9(7) doi: 10.1126/sciadv.ade2441
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| 2 |
Saskia Koene, Fabiënne Gwendolin Ropers, Jannelien Wieland, Tamara Rybak, Floor Wildschut, Dagmar Berghuis, Angela Morgan, Maria Pilar Trelles, Jeroen Ronald Scheepe, Regina Bökenkamp, Cacha M P C D Peeters-Scholte, Ruth Braden, Gijs W E Santen. Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals. Journal of Medical Genetics 2024; 61(4): 399 doi: 10.1136/jmg-2023-109537
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| 3 |
Shuliweeh Alenezi, Ahmed Alyahya, Hesham Aldhalaan. Autism Spectrum Disorder (ASD) and Attention Deficit Hyperactivity Disorder (ADHD) With Language Impairment Accompanied by Developmental Disability Caused by Forkhead Box Protein 1 (FOXP1) Exon Deletion: A Case Report. Cureus 2021; doi: 10.7759/cureus.20595
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Soudeh Ghafouri-Fard, Ashkan Pourtavakoli, Bashdar Mahmud Hussen, Mohammad Taheri, Seyed Abdulmajid Ayatollahi. A Review on the Role of Genetic Mutations in the Autism Spectrum Disorder. Molecular Neurobiology 2023; 60(9): 5256 doi: 10.1007/s12035-023-03405-9
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Zhenshan Ding, Binbin Jiao, Xuelong Chen, Xing Chen, Yangtian Jiao, Jianfeng Wang, Xiaofeng Zhou. The function of Foxp1 represses β-adrenergic receptor transcription in the occurrence and development of bladder cancer through STAT3 activity. Open Medicine 2023; 18(1) doi: 10.1515/med-2023-0647
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Filip Milanovic, Sinisa Ducic, Milena Jankovic, Sanja Sindjic-Antunovic, Emilija Dubljanin-Raspopović, Milica Aleksic, Goran Djuricic, Dejan Nikolic. Clinical Characteristics and Whole Exome Sequencing Analysis in Serbian Cases of Clubfoot Deformity—Single Center Study. Children 2024; 11(6): 647 doi: 10.3390/children11060647
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