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Luo, Zhenqing
85
results:
Search for persons
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Online (85)
Mediatypes
Articles (Online) (56)
Bookchapter (Online) (1)
OpenAccess-fulltext (28)
Sorted by: Relevance
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?
1
Mosaic variegated aneuploidy syndrome with tetraploid, and ..:
Guo, Jihong
;
He, Wen-Bin
;
Dai, Lei
...
Human Genetics and Genomics Advances. 5 (2024) 1 - p. 100256 , 2024
Link:
https://doi.org/10.1016/..
?
2
[Retracted] Applying Blockchain Technology in Network Publi..:
Luo, Zhenqing
;
Zhang, Cheng
;
Bhardwaj, Arpit
Computational Intelligence and Neuroscience. 2023 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1155/..
?
3
The Linkage between Carbon Market and Green Bond Market: Ev..:
Wu, Ding
;
Luo, Zhenqing
;
Zhang, Tidong
...
Sustainability. 15 (2023) 13 - p. 10634 , 2023
Link:
https://doi.org/10.3390/..
?
4
Novel Loss of Function (G15D) Mutation on RAC2 in a Family ..:
Duan, Xiaojun
;
Shen, Fang
;
Deng, Yafei
...
Journal of Clinical Immunology. 43 (2022) 3 - p. 604-614 , 2022
Link:
https://doi.org/10.1007/..
?
5
Case series of congenital pseudarthrosis of the tibia unful..:
Zheng, Yu
;
Zhu, Guanghui
;
Liu, Yaoxi
...
Human Genetics. 141 (2022) 8 - p. 1371-1383 , 2022
Link:
https://doi.org/10.1007/..
?
6
Mutant B3GALT6 in a Multiplex Family: A Dominant Variant Co..:
Shen, Fang
;
Yang, Yongjia
;
Zheng, Yu
...
Frontiers in Genetics. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
7
MECOM-related disorder: Radioulnar synostosis without hemat..:
Shen, Fang
;
Yang, Yongjia
;
Zheng, Yu
...
Genetics in Medicine. 24 (2022) 5 - p. 1139-1147 , 2022
Link:
https://doi.org/10.1016/..
?
8
A genotype and phenotype analysis of SMAD6 mutant patients ..:
Shen, Fang
;
Yang, Yongjia
;
Li, Pengcheng
...
Molecular Genetics & Genomic Medicine. 10 (2021) 1 - p. , 2021
Link:
https://doi.org/10.1002/..
?
9
Expanding the genotypes and phenotypes for 19 rare diseases..:
Liu, Juan
;
Zheng, Yu
;
Huang, Jiaotian
...
Human Mutation. 42 (2021) 11 - p. 1443-1460 , 2021
Link:
https://doi.org/10.1002/..
?
10
Disorder of Sexual Development Males With XYY in Blood Have..:
Yang, Yongjia
;
Chen, Fang
;
Luo, Zhenqing
...
Frontiers in Genetics. 12 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
?
11
Case report: two novel VPS13B mutations in a Chinese family..:
Zhao, Sha
;
Luo, Zhenqing
;
Xiao, Zhenghui
...
BMC Medical Genetics. 20 (2019) 1 - p. , 2019
Link:
https://doi.org/10.1186/..
?
12
High-Efficiency Monolayer Molybdenum Ditelluride Light-Emit..:
Zhu, Yi
;
Li, Ziyuan
;
Zhang, Linglong
...
ACS Applied Materials & Interfaces. 10 (2018) 50 - p. 43291-43298 , 2018
Link:
https://doi.org/10.1021/..
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13
Mosaic variegated aneuploidy syndrome with tetraploid, and ..:
Guo, Jihong
;
He, Wen-Bin
;
Dai, Lei
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10716027/. , 2023
Link:
http://www.ncbi.nlm.nih...
?
14
Mutant B3GALT6 in a Multiplex Family: A Dominant Variant Co..:
Shen, Fang
;
Yang, Yongjia
;
Zheng, Yu
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9207203/. , 2022
Link:
http://www.ncbi.nlm.nih...
?
15
Expanding the genotypes and phenotypes for 19 rare diseases..:
Liu, Juan
;
Zheng, Yu
;
Huang, Jiaotian
...
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9292147/. , 2021
Link:
http://www.ncbi.nlm.nih...
1-15