| For: | Luo MR, Dai SM, Li Y, Wang Q, Liu H, Gao P, Liu JY, Chen J, Zhao SJ, Yin GY. 3M syndrome patient with a novel mutation: A case report. World J Clin Cases 2024; 12(8): 1454-1460 [PMID: 38576808 DOI: 10.12998/wjcc.v12.i8.1454] |
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| URL: | https://www.wjgnet.com/2307-8960/full/v12/i8/1454.htm |
| Number | Citing Articles |
| 1 |
Shaymaa Elsayed, Gehad A. Elmakkawy, Ibrahim M. Abdelrazek, Dina A. Fawzy, JiHye Kim, YongJun Song, Omneya M. Omar, Ebtesam M. Abdalla. An Update on 3M Syndrome: Review of Clinical and Molecular Aspects and Report of Additional Families. American Journal of Medical Genetics Part A 2025; 197(8) doi: 10.1002/ajmg.a.64068
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| 2 |
Raghad Alhuthil, Afaf Alsagheir, Maha Almslam, Jana Raed, Farah Barakat, Sarah Murad, Bassam Bin-Abbas. 3M syndrome in Saudi Arabia: a case series study and literature review. Frontiers in Endocrinology 2025; 16 doi: 10.3389/fendo.2025.1666468
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| 3 |
Isabelle Bacchi, Sara Vandelli, Emanuele Coccia, Lucrezia Giannini, Roberta Zuntini, Rachele Teneggi, Stefano Giuseppe Caraffi, Maria Chiara Baroni, Gianluca Contrò, Adelaide Peruzzi, Irene Ambrosetti, Marzia Pollazzon, Chiara Sartori, Ekkehart Lausch, Uta Matysiak, Lucia Gambini, Giancarlo Gargano, Valeria Orlando, Antonio Novelli, Lorenzo Iughetti, Sheila Unger, Andrea Superti-Furga, Livia Garavelli. 3-M syndrome: evolution of the phenotype over time. Italian Journal of Pediatrics 2025; doi: 10.1186/s13052-025-02172-8
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