Weiwei Zang

Luoyang, China

Last Updated: 09/26/2026

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Found 8 publications

Incomplete Trisomy Rescue Reveals the Mechanism Underlying Discordance Between Noninvasive Prenatal Screening and Prenatal Diagnosis.

Incomplete Trisomy Rescue Reveals the Mechanism Underlying Discordance Between Noninvasive Prenatal Screening and Prenatal Diagnosis.

Journal: Molecular genetics & genomic medicine

Published: June 14, 2024

Familial exudative vitreoretinopathy caused by CTNNB1 gene de novo mutation in a Chinese family: a case report.

Familial exudative vitreoretinopathy caused by CTNNB1 gene de novo mutation in a Chinese family: a case report.

Journal: BMC pediatrics

Published: May 31, 2024

Genetic analysis and counseling of ADPKD caused by novel heterozygous mutations of PKD1 in two Chinese families: Case report.

Genetic analysis and counseling of ADPKD caused by novel heterozygous mutations of PKD1 in two Chinese families: Case report.

Journal: Heliyon

Published: May 30, 2024

Effect of clinical whole exome sequencing in aetiological investigation and reproductive risk prediction for a couple with monogenic inherited diseases.

Effect of clinical whole exome sequencing in aetiological investigation and reproductive risk prediction for a couple with monogenic inherited diseases.

Journal: Frontiers in genetics

Published: January 03, 2024

Genetic analysis of albinism caused by compound heterozygous mutations of the OCA2 gene in a Chinese family.

Genetic analysis of albinism caused by compound heterozygous mutations of the OCA2 gene in a Chinese family.

Journal: Hereditas

Published: August 29, 2023

Cat eye syndrome caused by 22q11.1q11.21 duplication: case report in a Chinese family.

Cat eye syndrome caused by 22q11.1q11.21 duplication: case report in a Chinese family.

Journal: Molecular cytogenetics

Published: July 10, 2023

Application of Copy Number Variation Sequencing Technology in 422 Foetuses with Abnormal Ultrasound Soft Markers.

Application of Copy Number Variation Sequencing Technology in 422 Foetuses with Abnormal Ultrasound Soft Markers.

Journal: International journal of women's health

Published: July 05, 2023

A novel variant of the SOX10 gene associated with Waardenburg syndrome type IV.

A novel variant of the SOX10 gene associated with Waardenburg syndrome type IV.

Journal: BMC medical genomics

Published: March 16, 2023

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Last Updated: 09/26/2026