Search Results - Chao-Chun Zou
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1
6q25.1-q25.3 Microdeletion in a Chinese Girl by Mian-Ling Zhong, Ye-Mei Song, Chao-Chun Zou
Published 2021Call Number: Loading…Connect to this object online.
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2
Recombinant Human Growth Hormone Therapy for Childhood Trichorhinophalangeal Syndrome Type I: A Case Report by Dan Huang, Jia Zhao, Fang-Ling Xia, Chao-Chun Zou
Published 2022Call Number: Loading…Connect to this object online.
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3
An unusual presentation of fucosidosis in a Chinese boy: a case report and literature review (childhood fucosidosis) by Shao-Jia Mao, Jia Zhao, Zheng Shen, Chao-Chun Zou
Published 2022Call Number: Loading…Connect to this object online.
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4
Report of one case with de novo mutation in TLK2 and literature review by Han-Yue Li, Chun-Ming Jiang, Ruo-Yan Liu, Chao-Chun Zou
Published 2024Call Number: Loading…Connect to this object online.
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5
Different AHO phenotype in a Chinese family with a novel GNAS missense variant: a case report by Qing Zhou, Bin Liang, Qing-Xian Fu, Hui Liu, Chao-Chun Zou
Published 2022Call Number: Loading…Connect to this object online.
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6
Case Report: Mucolipidosis II and III Alpha/Beta Caused by Pathogenic Variants in the GNPTAB Gene (Mucolipidosis) by Shao-Jia Mao, Yu-Mei Zu, Yang-Li Dai, Chao-Chun Zou
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7
Orthopedic manifestations in children with Prader-Willi syndrome by Miao Miao, Guo-Qiang Zhao, Qiong Zhou, Yun-Qi Chao, Chao-Chun Zou
Published 2024Call Number: Loading…Connect to this object online.
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8
Sepsis-induced Pancytopenia in an Adolescent Girl with Thyroid Storm: A Case Report by Qing Zhou, Li-Yong Zhang, Qing-Xian Fu, Chao-Chun Zou, Hui Liu
Published 2024Call Number: Loading…Connect to this object online.
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9
The diagnosis and management of mucopolysaccharidosis type II by Shao-Jia Mao, Qing-Qing Chen, Yang-Li Dai, Guan-Ping Dong, Chao-Chun Zou
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10
The influence of genotype makeup on the effectiveness of growth hormone therapy in children with Prader-Willi syndrome by Qiong Zhou, Yun-qi Chao, Yang-li Dai, Ying Gao, Zheng Shen, Guan-ping Dong, Chao-Chun Zou
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11
Case Report: De novo variant in myelin regulatory factor in a Chinese child with 46,XY disorder/difference of sex development, cardiac and urogenital anomalies, and short stature by Hui Wang, Dian Wu, De-Hua Wu, Hong-Juan Tian, Hai-Feng Li, Ke-Wen Jiang, Chao-Chun Zou
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