E-LIB Suche - Ergebnisse für: Zhang, Terry Jianguo

1

Diagnosis and treatment of the Ehlers-Danlos syndromes in C..:

Xu, Kexin ; Li, Guozhuang ; Wu, Zhihong...
Orphanet Journal of Rare Diseases. 19 (2024) 1 - p. , 2024

Link: https://doi.org/10.1186/..

2

Impaired glycine neurotransmission causes adolescent idiopa..:

Wang, Xiaolu ; Yue, Ming ; Cheung, Jason Pui Yin...
Journal of Clinical Investigation. 134 (2024) 2 - p. , 2024

Link: https://doi.org/10.1172/..

3

Rare variant association analyses reveal the significant co..:

Wen, Wen ; Zhao, Zhengye ; Zheng, Zhifa...
Journal of Medical Genetics. 61 (2024) 7 - p. 666-676 , 2024

Link: https://doi.org/10.1136/..

4

Corrigendum to Wu N, et al. The effect of pedicle screw ins..:

Wu, Nan ; Liu, Lian ; Chen, Guilin...
The Spine Journal. 24 (2024) 2 - p. 395 , 2024

Link: https://doi.org/10.1016/..

5

SIGMA leverages protein structural information to predict t..:

Zhao, Hengqiang ; Du, Huakang ; Zhao, Sen...
Cell Reports Methods. 4 (2024) 1 - p. 100687 , 2024

Link: https://doi.org/10.1016/..

6

An Efficient Muscle Segmentation Method Via Bayesian Fusion..:

Wang, Jinge ; Chen, Guilin ; Zhang, Terry Jianguo..
IEEE Transactions on Biomedical Engineering. , 2024

Link: https://doi.org/10.1109/..

7

First copy number variant in trans with single nucleotide v..:

Xu, Kexin ; Li, Guozhuang ; Niu, Yuchen...
American Journal of Medical Genetics Part A. , 2024

Link: https://doi.org/10.1002/..

8

COL11A2 as a candidate gene for vertebral malformations and..:

Rebello, Denise ; Wohler, Elizabeth ; Erfani, Vida...
Human Molecular Genetics. , 2023

Link: https://doi.org/10.1093/..

9

Retrospective Analysis of Associated Anomalies in 636 Patie..:

Wu, Nan ; Liu, Lian ; Zhang, Yuanqiang...
Journal of Bone and Joint Surgery. 105 (2023) 7 - p. 537-548 , 2023

Link: https://doi.org/10.2106/..

10

The effect of pedicle screw instrumentation at a young age ..:

Wu, Nan ; Liu, Lian ; Chen, Guilin...
The Spine Journal. 23 (2023) 9 - p. 1358-1364 , 2023

Link: https://doi.org/10.1016/..

11

Haplotype-specific MAPK3 expression in 16p11.2 deletion con..:

Liu, Fang ; Liang, Chen ; Li, Zhengchang...
Brain. , 2023

Link: https://doi.org/10.1093/..

12

Exome-wide Analysis of De Novo and Rare Genetic Variants in..:

Wang, Kun ; Zhao, Sen ; Xie, Zhixin...
Neurology. 98 (2022) 16 - p. , 2022

Link: https://doi.org/10.1212/..

13

Genetics of the Growing Spine:

, In: The Growing Spine,

Wu, Nan ; Zhang, Terry Jianguo ; Zhao, Sen. - p. 13-24 , 2022

Link: https://doi.org/10.1007/..

14

TBX6 as a cause of a combined skeletal‐kidney dysplasia syn..:

Li, Guozhuang ; Strong, Alanna ; Wang, Haojun...
American Journal of Medical Genetics Part A. 188 (2022) 12 - p. 3469-3481 , 2022

Link: https://doi.org/10.1002/..

15

Delineation of dual molecular diagnosis in patients with sk..:

Liu, Lian ; Sun, Liying ; Chen, Yujun...
Orphanet Journal of Rare Diseases. 17 (2022) 1 - p. , 2022

Link: https://doi.org/10.1186/..