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Lang, Yanhua
108
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Online (108)
Mediatypes
Articles (Online) (48)
OpenAccess-fulltext (60)
Sorted by: Relevance
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?
1
A novel heterozygous variant of the SALL1 gene with atypica..:
Liu, Xuyan
;
Wang, Hong
;
Zhang, Yiyin
...
Nephrology. 29 (2024) 8 - p. 541-546 , 2024
Link:
https://doi.org/10.1111/..
?
2
Three exonic variants in the COL4A5 gene alter RNA splicing..:
Zhang, Ran
;
Lang, Yanhua
;
Shi, Xiaomeng
...
Molecular Genetics & Genomic Medicine. 12 (2024) 2 - p. , 2024
Link:
https://doi.org/10.1002/..
?
3
Numerical analysis of a nonlinear age-structured HBV model ..:
Li, Wenli
;
Liu, Xing
;
Lang, Yanhua
Mathematics and Computers in Simulation. 225 (2024) - p. 250-266 , 2024
Link:
https://doi.org/10.1016/..
?
4
Four novel variants identified in primary hyperoxaluria and..:
Xin, Qing
;
Dong, Yameng
;
Guo, Wencong
...
Frontiers in Genetics. 14 (2023) - p. , 2023
Link:
https://doi.org/10.3389/..
?
5
Minigene splicing assays reveal new insights into exonic va..:
Shi, Xiaomeng
;
Wang, Hong
;
Zhang, Ruixiao
...
Molecular Genetics & Genomic Medicine. 11 (2023) 4 - p. , 2023
Link:
https://doi.org/10.1002/..
?
6
Identification of two novel variants of BCS1L gene in a pat..:
Guo, Wencong
;
Shao, Yingfei
;
Lang, Yanhua
...
Nephrology. 27 (2022) 10 - p. 810-814 , 2022
Link:
https://doi.org/10.1111/..
?
7
Genotypic and phenotypic analysis in 51 Chinese patients wi..:
Guo, Wencong
;
Song, Qijing
;
Zhang, Ruixiao
...
Clinical Genetics. 100 (2021) 4 - p. 440-446 , 2021
Link:
https://doi.org/10.1111/..
?
8
Sudden onset of nephrotic syndrome in an asymptomatic Fabry..:
Zhang, Ruixiao
;
Chen, Zeqing
;
Lang, Yanhua
...
Renal Failure. 42 (2020) 1 - p. 958-965 , 2020
Link:
https://doi.org/10.1080/..
?
9
Eight novel KCNJ1 variants and parathyroid hormone overacti..:
Zuo, Jianxin
;
Guo, Wencong
;
Wang, Shujuan
...
Clinica Chimica Acta. 511 (2020) - p. 248-254 , 2020
Link:
https://doi.org/10.1016/..
?
10
Thirteen novel CLCNKB variants and genotype/phenotype assoc..:
Han, Yue
;
Cheng, Hai
;
Shao, Shihong
...
Endocrine. 68 (2019) 1 - p. 192-202 , 2019
Link:
https://doi.org/10.1007/..
?
11
Eleven novel SLC12A1 variants and an exonic mutation cause ..:
Han, Yue
;
Zhao, Xiangzhong
;
Wang, Sai
...
Endocrine. 64 (2019) 3 - p. 708-718 , 2019
Link:
https://doi.org/10.1007/..
?
12
Familial hypomagnesaemia, Hypercalciuria and Nephrocalcinos..:
Lu, Jingru
;
Zhao, Xiangzhong
;
Paiardini, Alessandro
...
BMC Nephrology. 19 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1186/..
?
13
Novel compound heterozygous ATP6V1B1 mutations in a Chinese..:
Zhao, Xiangzhong
;
Lu, Jingru
;
Gao, Yanxia
...
BMC Nephrology. 19 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1186/..
?
14
Identification of a novel TSC2 c.3610G > A, p.G1204R mutati..:
Zhang, Ruixiao
;
Wang, Jianhong
;
Wang, Qing
...
BMC Medical Genetics. 19 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1186/..
?
15
A novel mutation in exon 9 of Cullin 3 gene contributes to ..:
Shao, Leping
;
Cui, Li
;
Lu, Jingru
...
FEBS Open Bio. 8 (2018) 3 - p. 461-469 , 2018
Link:
https://doi.org/10.1002/..
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