Hongqian Liu
6PUBLICATIONS
6CO-AUTHORS

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Publications (6)
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|Nov 13, 2024
Identification of a novel ST3GAL5 variant in a Chinese boy with GM3 synthase deficiency and literature review of variants in the ST3GAL5 gene.Dan Mu, Yanting Yang, Yao Liu
|Feb 09, 2024
Identification of copy number variations among fetuses with isolated ultrasound soft markers in pregnant women not of advanced maternal age.Yunyun Liu, Sha Liu, Jianlong Liu
|Aug 03, 2022
Impaired Function of a Rare Mutation in the MMUT Gene Causes Methylmalonic Acidemia in a Chinese Patient.Siyu Dai, Yanting Yang, Yaqian Li
|Mar 31, 2021
Noninvasive prenatal screening for fetal sex chromosome aneuploidies.Cechuan Deng, Sau Wai Cheung, Hongqian Liu
|Jul 01, 2020
Novel biallelic loss-of-function variants in CEP290 cause Joubert syndrome in two siblings.Xiang Wang, Zhu Zhang, Xueguang Zhang
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