For: | Yang LL, Liang SS. Study on pathogenic genes of dwarfism disease by next-generation sequencing. World J Clin Cases 2021; 9(7): 1600-1609 [PMID: 33728303 DOI: 10.12998/wjcc.v9.i7.1600] |
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URL: | https://www.wjgnet.com/2307-8960/full/v9/i7/1600.htm |
Number | Citing Articles |
1 |
Yurong Piao, Rongmin Li, Yingjie Wang, Congli Chen, Yanmei Sang. Novel OBSL1 Variant in a Chinese Patient with 3M Syndrome and the c.458dupG Mutation May Be a Potential Hotspot Mutation in the Chinese Population. Journal of Clinical Research in Pediatric Endocrinology 2024; : 0 doi: 10.4274/jcrpe.galenos.2024.2023-11-6
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2 |
Shan Li, Yueyang Sheng, Xinyu Wang, Qianqian Wang, Ying Wang, Yanzhuo Zhang, Chengai Wu, Xu Jiang. Biallelic variants in SLC26A2 cause multiple epiphyseal dysplasia-4 by disturbing chondrocyte homeostasis. Orphanet Journal of Rare Diseases 2024; 19(1) doi: 10.1186/s13023-024-03228-4
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3 |
M. Willems, C. Amouroux, M. Barat-Houari, J.-P. Salles, T. Edouard. Exploring the genetic causes of isolated short stature. What has happened to idiopathic short stature?. Archives de Pédiatrie 2022; 28(8): 28/8S27 doi: 10.1016/S0929-693X(22)00040-9
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4 |
Endashaw Terefe, Gurja Belay, Jianlin Han, Olivier Hanotte, Abdulfatai Tijjani. Genomic adaptation of Ethiopian indigenous cattle to high altitude. Frontiers in Genetics 2022; 13 doi: 10.3389/fgene.2022.960234
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