For: | Ge XY, Ge L, Hu WW, Li XL, Hu YY. Growth hormone therapy for children with KBG syndrome: A case report and review of literature. World J Clin Cases 2020; 8(6): 1172-1179 [PMID: 32258089 DOI: 10.12998/wjcc.v8.i6.1172] |
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URL: | https://www.wjgnet.com/2307-8960/full/v8/i6/1172.htm |
Number | Citing Articles |
1 |
Yunha Choi, Jungmin Choi, Hyosang Do, Soojin Hwang, Go Hun Seo, In Hee Choi, Changwon Keum, Jin‐Ho Choi, Minji Kang, Gu‐Hwan Kim, Han‐Wook Yoo, Beom Hee Lee. KBG syndrome: Clinical features and molecular findings in seven unrelated Korean families with a review of the literature. Molecular Genetics & Genomic Medicine 2023; 11(4) doi: 10.1002/mgg3.2127
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2 |
Davide Mattei, Paolo Cavarzere, Rossella Gaudino, Franco Antoniazzi, Giorgio Piacentini. DYSMORPHIC features and adult short stature: possible clinical markers of KBG syndrome. Italian Journal of Pediatrics 2021; 47(1) doi: 10.1186/s13052-021-00961-5
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3 |
Stephanie Ho, Ho‐Ming Luk, Ivan F. M. Lo. KBG syndrome in a Chinese population: A case series. American Journal of Medical Genetics Part A 2022; 188(6): 1693 doi: 10.1002/ajmg.a.62688
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4 |
Su Jin Kim, Aram Yang, Ji Sun Park, Dae Gyu Kwon, Jeong-Seop Lee, Young Se Kwon, Ji Eun Lee. Two Novel Mutations of ANKRD11 Gene and Wide Clinical Spectrum in KBG Syndrome: Case Reports and Literature Review. Frontiers in Genetics 2020; 11 doi: 10.3389/fgene.2020.579805
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5 |
Fenqi Gao, Xiu Zhao, Bingyan Cao, Xin Fan, Xiaoqiao Li, Lele Li, Shengbin Sui, Zhe Su, Chunxiu Gong. Genetic and Phenotypic Spectrum of KBG Syndrome: A Report of 13 New Chinese Cases and a Review of the Literature. Journal of Personalized Medicine 2022; 12(3): 407 doi: 10.3390/jpm12030407
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