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Clinical and genetic features of Prader-Willi syndrome in China. [electronic resource] by
- Lu, Wei
- Qi, Yan
- Cui, Bing
- Chen, Xiu-Li
- Wu, Bing-Bing
- Chen, Chao
- Cao, Yun
- Zhou, Wen-Hao
- Xu, Hong
- Luo, Fei-Hong
Producer: 20141024
In:
European journal of pediatrics vol. 173
Availability: No items available.
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18.
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A Specially Designed Multi-Gene Panel Facilitates Genetic Diagnosis in Children with Intrahepatic Cholestasis: Simultaneous Test of Known Large Insertions/Deletions. [electronic resource] by
- Wang, Neng-Li
- Lu, Yu-Lan
- Zhang, Ping
- Zhang, Mei-Hong
- Gong, Jing-Yu
- Lu, Yi
- Xie, Xin-Bao
- Qiu, Yi-Ling
- Yan, Yan-Yan
- Wu, Bing-Bing
- Wang, Jian-She
Producer: 20170620
In:
PloS one vol. 11
Availability: No items available.
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Identification of eight novel mutations in 11 Chinese patients with maple syrup urine disease. [electronic resource] by
- Sun, Wei-Hua
- Wu, Bing-Bing
- Wang, Ya-Qiong
- Wu, Meng-Yuan
- Dong, Xin-Ran
- Zhang, Yue-Ping
- Lu, Wei
- Zhang, Ping
- Yang, Bin
- Zhang, Min
- Wu, Hong-Jiang
- Zhou, Wen-Hao
Producer: 20210722
In:
World journal of pediatrics : WJP vol. 16
Availability: No items available.
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Single-cell analysis reveals a nestin [electronic resource] by
- Yin, Zi
- Hu, Jia-Jie
- Yang, Long
- Zheng, Ze-Feng
- An, Cheng-Rui
- Wu, Bing-Bing
- Zhang, Can
- Shen, Wei-Liang
- Liu, Huan-Huan
- Chen, Jia-Lin
- Heng, Boon Chin
- Guo, Guo-Ji
- Chen, Xiao
- Ouyang, Hong-Wei
Producer: 20180709
In:
Science advances vol. 2
Availability: No items available.
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