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Qian, Yeqing
265
results:
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Online (265)
Mediatypes
Articles (Online) (136)
Bookchapter (Online) (2)
OpenAccess-fulltext (127)
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?
1
An efficient molecular genetic testing strategy for inconti..:
Chen, Min
;
Tan, Mei-Hua
;
Liu, Jiao
...
npj Genomic Medicine. 9 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1038/..
?
2
Identification of four TTN variants in three families with ..:
Fan, Lihong
;
Li, Haibo
;
Xu, Ying
...
BMC Medical Genomics. 17 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1186/..
?
3
Limb girdle muscular dystrophy 23 caused by compound hetero..:
Xu, Yuqing
;
Zhu, Linyan
;
Qian, Yeqing
.
Frontiers in Pediatrics. 11 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
4
Noninvasive Prenatal Screening for Common Fetal Aneuploidie..:
Qian, Yeqing
;
Liu, Yongfeng
;
Yan, Kai
...
Laboratory Investigation. 103 (2023) 4 - p. 100043 , 2023
Link:
https://doi.org/10.1016/..
?
5
Prenatal diagnosis of Walker–Warburg syndrome due to compou..:
Wang, Peng
;
Jin, Pengzhen
;
Zhu, Linyan
...
The Journal of Gene Medicine. 24 (2022) 5 - p. , 2022
Link:
https://doi.org/10.1002/..
?
6
Case Report: Prenatal diagnosis of fetal tetrasomy 9p initi..:
Yu, Jialing
;
Chen, Na
;
Chen, Min
...
Frontiers in Genetics. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
7
Case Report: Prenatal Diagnosis of Postaxial Polydactyly Wi..:
Fan, Lihong
;
Jin, Pengzhen
;
Qian, Yeqing
...
Frontiers in Genetics. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
8
Case report: FOXP1 syndrome caused by a de novo splicing va..:
Chen, Min
;
Sun, Yixi
;
Qian, Yeqing
...
Frontiers in Genetics. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
9
Case Report: Novel splicing mutations in RFX5 causing MHC c..:
Chen, Shan
;
Xu, Yuqing
;
Qian, Yeqing
..
Frontiers in Genetics. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
10
Influence of driving style on traffic flow fuel consumption..:
Yang, Yichen
;
Cao, Tianyu
;
Xu, Shangzhi
..
Physica A: Statistical Mechanics and its Applications. 599 (2022) - p. 127520 , 2022
Link:
https://doi.org/10.1016/..
?
11
Case report: Prenatal diagnosis of fetal intracranial hemor..:
Xu, Min
;
Jin, Pengzhen
;
Huang, Yingzhi
...
Frontiers in Genetics. 13 (2022) - p. , 2022
Link:
https://doi.org/10.3389/..
?
12
Identification of of a PAX2 mutation from maternal mosaicis..:
Liu, Bei
;
Chen, Mengjia
;
Yang, Yanmei
...
Clinica Chimica Acta. 525 (2022) - p. 23-28 , 2022
Link:
https://doi.org/10.1016/..
?
13
Novel deep intronic and frameshift mutations causing a TRIP..:
Qian, Yeqing
;
Hu, Gang
;
Chen, Min
...
American Journal of Medical Genetics Part A. 185 (2021) 8 - p. 2482-2487 , 2021
Link:
https://doi.org/10.1002/..
?
14
Clinical Efficiency of Non-invasive Prenatal Screening for ..:
Xu, Yanfei
;
Jin, Pengzhen
;
Lei, Yu
...
Frontiers in Genetics. 12 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
?
15
Case Report: A Synonymous Mutation in NF1 Located at the No..:
Jin, Pengzhen
;
Yan, Kai
;
Ye, Shaofen
...
Frontiers in Genetics. 12 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
1-15