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Cited by in CrossRef
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]
URL: https://www.wjgnet.com/2307-8960/full/v8/i6/1172.htm
Number Citing Articles
1
Dongye He, Mei Zhang, Yanying Li, Fupeng Liu, Bo Ban. Insights into the ANKRD11 variants and short-stature phenotype through literature review and ClinVar database searchOrphanet Journal of Rare Diseases 2024; 19(1) doi: 10.1186/s13023-024-03301-y
2
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 literatureMolecular Genetics & Genomic Medicine 2023; 11(4) doi: 10.1002/mgg3.2127
3
Davide Mattei, Paolo Cavarzere, Rossella Gaudino, Franco Antoniazzi, Giorgio Piacentini. DYSMORPHIC features and adult short stature: possible clinical markers of KBG syndromeItalian Journal of Pediatrics 2021; 47(1) doi: 10.1186/s13052-021-00961-5
4
Stephanie Ho, Ho‐Ming Luk, Ivan F. M. Lo. KBG syndrome in a Chinese population: A case seriesAmerican Journal of Medical Genetics Part A 2022; 188(6): 1693 doi: 10.1002/ajmg.a.62688
5
Marie Adamo-Croux, Adriane Auger-Gilli, Gwenaël Le Guyader, Juliette Aubin-Courjault, Henri Margot, Claire Bar, Didier Lacombe, Julien Van-Gils, Marine Legendre, Aurélien Binet, Xavier Le Guillou Horn. Care pathways in childhood neurodevelopmental disorders: Toward greater awareness of KBG syndrome among pediatriciansArchives de Pédiatrie 2024; 31(5): 320 doi: 10.1016/j.arcped.2024.02.007
6
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 ReviewFrontiers in Genetics 2020; 11 doi: 10.3389/fgene.2020.579805
7
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 LiteratureJournal of Personalized Medicine 2022; 12(3): 407 doi: 10.3390/jpm12030407