Zailong Qin
8PUBLICATIONS
9CO-AUTHORS
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Publications (8)
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|Jan 29, 2024
A genetic variant in the MAST1 gene is associated with mega-corpus-callosum syndrome with hypoplastic cerebellar vermis, in a fetus.Sheng Yi, Xianglian Tang, Fei Chen
|Jun 18, 2023
Early onset horizontal gaze palsy and progressive scoliosis due to a noncanonical splicing-site variant and a missense variant in the ROBO3 gene.Sheng Yi, Zailong Qin, Xunzhao Zhou
|May 12, 2021
A novel and recurrent KLHL40 pathogenic variants in a Chinese family of multiple affected neonates with nemaline myopathy 8.Sheng Yi, Yue Zhang, Zailong Qin
|Mar 16, 2021
Novel compound heterozygous frameshift variants in WDR81 associated with congenital hydrocephalus 3 with brain anomalies: First Chinese prenatal case confirms WDR81 involvement.Jiasun Su, Weiliang Lu, Mengting Li
|Nov 18, 2020
Whole-exome sequencing identified novel compound heterozygous variants in a Chinese neonate with liver failure and review of literature.Zailong Qin, Qi Yang, Shang Yi
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