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Journal of Clinical Laboratory Analysis|September 27, 2019
Development and validation of a haplotype-free technique for non-invasive prenatal diagnosis of spinal muscular atrophyXianda Wei, Weigang Lv, Hu Tan, et al.
Molecular Genetics & Genomic Medicine|March 2, 2022
Phenotypic variability of syndromic craniosynostosis caused by c.833G > T in FGFR2: Clinical and genetic evaluation of eight patients from a five-generation familyXianda Wei, Guori Huang, Baoheng Gui, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 15, 2015
Clinical and molecular investigation in Chinese patients with glutaric aciduria type IYanghui Zhang, Haoxian Li, Ruiyu Ma, et al.
Familial Cancer|February 11, 2017
A lesson from a reported pathogenic variant in Peutz-Jeghers syndrome: a case reportHu Tan, Xianda Wei, Pu Yang, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|December 17, 2016
WDR73 missense mutation causes infantile onset intellectual disability and cerebellar hypoplasia in a consanguineous familyChen Jiang, Nan Gai, Yongyi Zou, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 4, 2024
[Analysis of a child with DIGFAN syndrome due to variant of MORC2 gene]Bobo Xie, Xin Fan, Xianda Wei, et al.
Journal of Genetic Counseling|July 17, 2016
Notable Carrier Risks for Individuals Having Two Copies of SMN1 in Spinal Muscular Atrophy Families with 2-copy Alleles: Estimation Based on Chinese Meta-analysis DataXianda Wei, Hu Tan, Pu Yang, et al.
Scientific Reports|July 2, 2025
Genetic skeletal disorders: phenotypic-genotypic characteristics and RhGH therapy responses of a pediatric cohortYiyun Huang, Yan Peng, Chuan Li, et al.
Biomarkers in Medicine|July 11, 2025
Evaluation of the diagnostic efficacy of serum DR-70 and its combination with CEA in lung cancerXuena Wang, Xianda Wei, Zifeng Cheng, et al.
Molecular Genetics & Genomic Medicine|August 1, 2019
Molecular investigation in Chinese patients with primary carnitine deficiencyYanghui Zhang, Haoxian Li, Jing Liu, et al.
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