Search Results - Weiwei Zang

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  1. 1

    A novel variant of the SOX10 gene associated with Waardenburg syndrome type IV by Yanan Wang, Yuqiong Chai, Pai Zhang, Weiwei Zang

    Published in BMC Medical Genomics (2023-06-01)
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  2. 2

    Cat eye syndrome caused by 22q11.1q11.21 duplication: case report in a Chinese family by Yanan Wang, Pai Zhang, Yuqiong Chai, Weiwei Zang

    Published in Molecular Cytogenetics (2023-10-01)
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  3. 3

    Genetic analysis and counseling of ADPKD caused by novel heterozygous mutations of PKD1 in two Chinese families: Case report by Yanan Wang, Jiapei Jin, Yuqiong Chai, Pai Zhang, Weiwei Zang

    Published in Heliyon (2024-11-01)
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  4. 4

    Genetic analysis of albinism caused by compound heterozygous mutations of the OCA2 gene in a Chinese family by Yanan Wang, Yujie Chang, Mingya Gao, Weiwei Zang, Xiaofei Liu

    Published in Hereditas (2024-02-01)
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  5. 5

    Effect of clinical whole exome sequencing in aetiological investigation and reproductive risk prediction for a couple with monogenic inherited diseases by Yanan Wang, Yuqiong Chai, Jieqiong Wang, Mingya Gao, Weiwei Zang, Yujie Chang

    Published in Frontiers in Genetics (2024-05-01)
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  6. 6

    Familial exudative vitreoretinopathy caused by CTNNB1 gene de novo mutation in a Chinese family: a case report by Yanan Wang, Yujie Chang, Hongtao Lei, Weiyan Yan, Yuqiong Chai, Weiwei Zang

    Published in BMC Pediatrics (2025-02-01)
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  7. 7

    Incomplete Trisomy Rescue Reveals the Mechanism Underlying Discordance Between Noninvasive Prenatal Screening and Prenatal Diagnosis by Yanan Wang, Yong Zhou, Yuqiong Chai, Weiwei Zang, Hongchao Wang, Fan Yin, Qianqian Tan, Zhigang Chen

    Published in Molecular Genetics & Genomic Medicine (2025-03-01)
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