Search Results - Mengxia Ni
- Showing 1 - 2 results of 2
-
1
A novel compound heterozygous mutation of the SMARCAL1 gene leading to mild Schimke immune-osseous dysplasia: a case report by Shuaimei Liu, Mingchao Zhang, Mengxia Ni, Peiran Zhu, Xinyi Xia
Published 2017Call Number: Loading…Connect to this object online.
Located: Loading…
Book -
2
The susceptibility of FSHB -211G > T and FSHR G-29A, 919A > G, 2039A > G polymorphisms to men infertility: an association study and meta-analysis by Qiuyue Wu, Jing Zhang, Peiran Zhu, Weijun Jiang, Shuaimei Liu, Mengxia Ni, Mingchao Zhang, Weiwei Li, Qing Zhou, Yingxia Cui, Xinyi Xia
Published 2017Call Number: Loading…Connect to this object online.
Located: Loading…
Book