Author/Creator: Lv, Weigang - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Lv, Weigang

1. An Xp21.3p11.4 duplication observed in a boy with intellectual deficiency and speech delay and his asymptomatic mother. Issue 7 (4th July 2013)

Authors:: Wu, Lingqian; Liu, Jing; Lv, Weigang; Wen, Juan; Xia, Yan; Liang, Desheng
Journal:: Birth defects research
Issue:: Volume 97:Issue 7(2013:Jul.)
Page Start:: 467
Record Type:: Journal Article
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2. Chrysophanol attenuates airway inflammation and remodeling through nuclear factor‐kappa B signaling pathway in asthma. (17th July 2019)

Authors:: Song, Guihua; Zhang, Yan; Yu, Suping; Lv, Weigang; Guan, Zhiwei; Sun, Mengmeng; Wang, Jing
Journal:: Phytotherapy research
Issue:: Volume 33:Number 10(2019)
Page Start:: 2702
Record Type:: Journal Article
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3. Development and validation of a haplotype‐free technique for non‐invasive prenatal diagnosis of spinal muscular atrophy. Issue 2 (25th September 2019)

Authors:: Wei, Xianda; Lv, Weigang; Tan, Hu; Liang, Desheng; Wu, Lingqian
Journal:: Journal of clinical laboratory analysis
Issue:: Volume 34:Issue 2(2020)
Page Start:: n/a
Record Type:: Journal Article
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4. Noninvasive Prenatal Testing for Wilson Disease by Use of Circulating Single-Molecule Amplification and Resequencing Technology (cSMART). (6th January 2020)

Authors:: Lv, Weigang; Wei, Xianda; Guo, Ruolan; Liu, Qin; Zheng, Yu; Chang, Jiazhen; Bai, Ting; Li, Haoxian; Zhang, Jianguang; Song, Zhuo; Cram, David S; Liang, Desheng; Wu, Lingqian
Journal:: Clinical chemistry
Issue:: Volume 61:Number 1(2015)
Page Start:: 172
Record Type:: Journal Article
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5. Non‐invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing. (9th January 2013)

Authors:: Liang, Desheng; Lv, Weigang; Wang, Hua; Xu, Liangpu; Liu, Jing; Li, Haoxian; Hu, Liang; Peng, Ying; Wu, Lingqian
Journal:: Prenatal diagnosis
Issue:: Volume 33:Number 5(2013:May)
Page Start:: 409
Record Type:: Journal Article
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6. Renal Expression of CLC-5 and Megalin/Cubilin in Dent-1 Disease With Nonsense Mutations of CLCN5 Gene. (July 2022)

Authors:: Zhai, Panpan; Lv, Weigang; Yang, Xiaoqing; Huang, Yanjie; Zhai, Wensheng; Ren, Xianqing; Zhang, Xia; Yang, Meng; Zhang, Jian; Guo, Ting; Bai, Minghui; Yang, Yueli; Ding, Ying; Huang, Yanshi
Journal:: Pediatric and developmental pathology
Issue:: Volume 25:Number 4(2022)
Page Start:: 397
Record Type:: Journal Article
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