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Author/Creator Lu, Yulan

11. Clinical exome sequencing as the first-tier test for diagnosing developmental disorders covering both CNV and SNV: a Chinese cohort. Issue 8 (31st January 2020)

Authors:
Dong, Xinran; Liu, Bo; Yang, Lin; Wang, Huijun; Wu, Bingbing; Liu, Renchao; Chen, Hongbo; Chen, Xiang; Yu, Sha; Chen, Bin; Wang, Sujuan; Xu, Xiu; Zhou, Wenhao; Lu, Yulan
Journal:
Journal of medical genetics
Issue:
Volume 57:Issue 8(2020)
Page Start:
558
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

12. Clinical exome sequencing identifies novel CREBBP variants in 18 Chinese Rubinstein–Taybi Syndrome kids with high frequency of polydactyly. Issue 12 (22nd October 2019)

Authors:
Yu, Sha; Wu, Bingbing; Qian, Yanyan; Zhang, Ping; Lu, Yulan; Dong, Xinran; Wang, Qing; Zhao, Xuemei; Liu, Renchao; Zhou, Wenhao; Wang, Huijun
Journal:
Molecular genetics & genomic medicine
Issue:
Volume 7:Issue 12(2019)
Page Start:
n/a
Record Type:
Journal Article
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15. Cover, Volume 42, Issue 4. Issue 4 (15th April 2021)

Authors:
Wang, Huijun; Xiao, Feifan; Dong, Xinran; Lu, Yulan; Cheng, Guoqiang; Wang, Laishuan; Lu, Wei; Yang, Lin; Chen, Liping; Kang, Wenqing; Li, Long; Pan, Xinnian; Wei, Qiufen; Zhuang, Deyi; Chen, Dongmei; Yin, Zhaoqing; Yang, Ling; Ni, Qi; Liu, Renchao; Li, Gang
Journal:
Human mutation
Issue:
Volume 42:Issue 4(2021)
Page Start:
i
Record Type:
Journal Article
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16. Diagnostic and clinical utility of next‐generation sequencing in children born with multiple congenital anomalies in the China neonatal genomes project. Issue 4 (4th February 2021)

Authors:
Wang, Huijun; Xiao, Feifan; Dong, Xinran; Lu, Yulan; Cheng, Guoqiang; Wang, Laishuan; Lu, Wei; Yang, Lin; Chen, Liping; Kang, Wenqing; Li, Long; Pan, Xinnian; Wei, Qiufen; Zhuang, Deyi; Chen, Dongmei; Yin, Zhaoqing; Yang, Ling; Ni, Qi; Liu, Renchao; Li, Gang
Journal:
Human mutation
Issue:
Volume 42:Issue 4(2021)
Page Start:
434
Record Type:
Journal Article
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19. Genetic architecture in neonatal intensive care unit patients with congenital heart defects: a retrospective study from the China Neonatal Genomes Project. Issue 3 (20th May 2022)

Authors:
Wang, Huijun; Xiao, Feifan; Qian, Yanyan; Wu, Bingbing; Dong, Xinran; Lu, Yulan; Cheng, Guoqiang; Wang, Laishuan; Yan, Kai; Yang, Lin; Chen, Liping; Kang, Wenqing; Li, Long; Pan, Xinnian; Wei, Qiufen; Zhuang, Deyi; Chen, Dongmei; Yin, Zhaoqing; Yang, Ling; Ni, Qi
Journal:
Journal of medical genetics
Issue:
Volume 60:Issue 3(2023)
Page Start:
247
Record Type:
Journal Article
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20. High-risk phenotypes of genetic disease in a Neonatal Intensive Care Unit population. Issue 5 (5th March 2022)

Authors:
Xiao, Tiantian; Ni, Qi; Chen, Huiyao; Wang, Huijun; Yang, Lin; Wu, Bingbing; Cao, Yun; Cheng, Guoqiang; Wang, Laishuan; Hu, Liyuan; Mei, Hongfang; Lu, Yulan; Gong, Mengchun; Dong, Xinran; Zhou, Wenhao
Editors:
Ni, Jing
Journal:
Chinese medical journal
Issue:
Volume 135:Issue 5(2022)
Page Start:
625
Record Type:
Journal Article
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