X. Zhou

Novel compound heterozygous frameshift variants in WDR81 associated with congenital hydrocephalus 3 with brain anomalies: First Chinese prenatal case confirms WDR81 involvement

Yiping Shen, Z. Qin, Jiasun Su, 2021, Molecular genetics & genomic medicine.

Clinical application of whole-exome sequencing: A retrospective, single-center study

Z. Qin, Jiasun Su, Qiang Zhang, 2021, Experimental and therapeutic medicine.

Two novel compound heterozygous variants of LTBP4 in a Chinese infant with cutis laxa type IC and a review of the related literature

Z. Qin, Jiasun Su, Qiang Zhang, 2020, BMC Medical Genomics.

Case Report: Variations in the ALPL Gene in Chinese Patients With Hypophosphatasia

Z. Qin, Qiang Zhang, Shang Yi, 2021, Frontiers in Genetics.

Two novel compound heterozygous variants of LTBP4 in a Chinese infant with cutis laxa type IC and a review of the related literature

Z. Qin, Qiang Zhang, Shang Yi, 2020, BMC medical genomics.

Early onset horizontal gaze palsy and progressive scoliosis due to a noncanonical splicing‐site variant and a missense variant in the ROBO3 gene

Z. Qin, Qinle Zhang, Shang Yi, 2023, Molecular genetics & genomic medicine.

Clinical and molecular analysis of Guangxi patients with Kabuki syndrome and KMT2D mutations

Xiaofei Zhang, Qiang Zhang, Z. Qin, 2023, Heliyon.