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Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|December 15, 2015
[Misdiagnosis of mosaic tetrasomy 9p in a fetus by single nucleotide polymorphism-based array]Jianzhu Wu, Yingjun Xie, Baojiang Chen
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 30, 2015
[Prenatal diagnosis of five cases of monochorionic-diamniotic twins discordant for karyotype analysis]Jianzhu Wu, Yi Zhou, Shaobin Lin, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 7, 2016
[Prenatal diagnosis of 1p36.3 microdeletion in a fetus with complex heart defect]Jianzhu Wu, Zhiming He, Shaobin Lin, et al.
Molecular Medicine Reports|November 12, 2014
When Cri du chat syndrome meets Edwards syndromeYingjun Xie, Yi Zhou, Jianzhu Wu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 11, 2014
[Cytogenetic and molecular study of a patient with severe oligozoospermia and asthenozoospermia]Shaobin Lin, Yingjun Xie, Jianzhu Wu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|September 1, 2016
[Application of single nucleotide polymorphism-based array analysis for prenatal diagnosis of a fetus with de novo derivative chromosome]Jianzhu Wu, Zhiming He, Zhiqiang Zhang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|February 11, 2017
[Prenatal genetic analysis of two fetuses with Miller-Dieker syndrome]Shaobin Lin, Yanmin Luo, Jianzhu Wu, et al.
Molecular Medicine Reports|October 26, 2016
Chromosome 10q26 deletion syndrome: Two new cases and a review of the literatureShaobin Lin, Yi Zhou, Qun Fang, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics|June 7, 2016
[Genetic analysis of a fetus with partial 1q monosomy and partial 17q trisomy]Shaobin Lin, Zhiqiang Zhang, Jianzhu Wu, et al.
Molecular Medicine Reports|November 18, 2015
Smith‑Magenis syndrome in monozygotic twin fetuses presenting with discordant phenotypes and uteroplacental insufficiencyYi Zhou, Yingjun Xie, Yunxiao Zhu, et al.
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