Qiuling Zhao

发表

Two novel BTD mutations causing profound biotinidase deficiency in a Chinese patient

Yi Zhao, Yu Lu, Huijun Yuan, 2021, Molecular genetics & genomic medicine.

Prenatal diagnosis identifies compound heterozygous variants in RYR1 that causes ultrasound abnormalities in a fetus

Yong-yi Ma, Xu Zhang, Xiaoduo Li, 2022, BMC Medical Genomics.

Identification of a complex genomic rearrangement in TMPRSS3 by massively parallel sequencing in Chinese cases with prelingual hearing loss

Huijun Yuan, Jing Cheng, Yu Lu, 2019, Molecular genetics & genomic medicine.