A Multidisciplinary Approach in Prenatal Diagnosis of TSC With Cardiac Rhabdomyoma as the Initial Symptom

by Yiming Qi, Yiming Qi, Hongke Ding, Hongke Ding, Yanlin Huang, Yanlin Huang, Yukun Zeng, Lihua Yu, Ling Liu, Yan Zhang, Aihua Yin, Aihua Yin
Published 2021-08-01

Mutations in both SAMD9 and SLC19A2 genes caused complex phenotypes characterized by recurrent infection, dysphagia and profound deafness – a case report for dual diagnosis

by Yan Zhang, Yi Zhang, Victor Wei Zhang, Chunyi Zhang, Hongke Ding, Aihua Yin
Published 2019-10-01

A Novel Multi-Exon Deletion of PACS1 in a Three-Generation Pedigree: Supplements to PACS1 Neurodevelopmental Disorder Spectrum

by Yuan Liu, Yuan Liu, Hongke Ding, Hongke Ding, Tizhen Yan, Ling Liu, Ling Liu, Lihua Yu, Lihua Yu, Yanlin Huang, Yanlin Huang, Fake Li, Fake Li, Yukun Zeng, Yukun Zeng, Weiwei Huang, Weiwei Huang, Yan Zhang, Yan Zhang, Aihua Yin, Aihua Yin
Published 2021-07-01

Severe fetal anemia and hydrops fetalis associated with compound heterozygosity for Hb Zurich-Albisrieden (:c.178G>C) and Hb Quong Sze (:c.377T>C)

by Li Du, Xiuqin Bao, Wei He, Danqing Qin, Jicheng Wang, Ying Xiong, Xiaomei Shi, Hongke Ding, Cuize Yao, Jing Wu
Published 2021-07-01

Development of a community-based hearing loss prevention and control service model in Guangdong, China

by Chang Liu, Anshi Wang, Yanlin Huang, Yan Zhang, Hongke Ding, Jing Wu, Li Du, Jie Yang, Fei Mai, Yukun Zeng, Ling Liu, Xin Zhao, Changbin Zhang, Aihua Yin
Published 2019-11-01

Genetic testing for Prader-Willi syndrome and Angelman syndrome in the clinical practice of Guangdong Province, China

by Chang Liu, Xiangzhong Zhang, Jicheng Wang, Yan Zhang, Anshi Wang, Jian Lu, Yanlin Huang, Shu Liu, Jing Wu, Li Du, Jie Yang, Hongke Ding, Ling Liu, Xin Zhao, Aihua Yin
Published 2019-02-01