13-染色體缺失綜合征合并視網膜母細胞瘤一例_Chinese Journal of Ocular Fundus Diseases

Authors：

要青清 , 程湧 , 令狐丹丹 , 朱雪梅 , 鄧洵 ,  梁建宏

北京大學人民醫院眼科 100044;
要青清，現在邯鄲市第一醫院眼科 056002;

Corresponding?author：

梁建宏, Email: drliangjianhong@126.com

Keywords：

染色體缺失; 視網膜母細胞瘤; 病例報告

DOI：

10.3760/cma.j.cn511434-20190711-00221

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Citation： 要青清, 程湧, 令狐丹丹, 朱雪梅, 鄧洵, 梁建宏. 13-染色體缺失綜合征合并視網膜母細胞瘤一例. Chinese Journal of Ocular Fundus Diseases, 2020, 36(10): 804-805. doi: 10.3760/cma.j.cn511434-20190711-00221 Copy

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2.	Lévy J, Haye D, Marziliano N, et al. EFNB2 haploinsufficiency causes a syndromic neurodevelopmental disorder[J]. Clin Genet, 2018, 93(6): 1141-1147. DOI: 10.1111/cge.13234.
3.	Jones K, Minassian BA. Genetic testing in infantile spasms identifies a chromosome 13q deletion and retinoblastoma[J]. Pediatr Neurol, 2014, 50(5): 522-524. DOI: 10.1016/j.pediatrneurol.2013.11.018.
4.	Abramson DH, Shield CL, Munier FL, et al. Treatment of retinoblastoma in 2015: agreement and disagreement[J]. JAMA Ophthalmol, 2015, 133(11): 1341-1347. DOI: 10.1001/Jamaophthalmol.2015.3108.

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Chinese Journal of Ocular Fundus Diseases

13-染色體缺失綜合征合并視網膜母細胞瘤一例

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