Clinical exome sequencing identifies novel compound heterozygous mutations of the WEE2 gene in primary infertile women with fertilization failure-Reference-Cited by-同舟云学术

Clinical exome sequencing identifies novel compound heterozygous mutations of the WEE2 gene in primary infertile women with fertilization failure

Author:

Wang Ancong¹²,Huang Shan³,Liu Min¹²,Wang Baosong¹²,Wu Fengxia⁴,Zhu Dongyi¹²,Zhao Xiangyu⁵^ORCID

Affiliation:

1. Department of Reproductive Medicine, Linyi People’s Hospital, Linyi, PR China

2. Department of Obstetrics and Gynecology, Linyi People’s Hospital, Linyi, PR China

3. Department of Respiratory Medicine, Linyi Hospital of traditional Chinese Medicine, Linyi, PR China

4. Department of Anatomy and Neurobiology, School of Basic Medical Science, Shandong University, Jinan, PR China

5. Department of Medical Genetics, Linyi People’s Hospital, Linyi, PR China

Funder

Shandong Provincial Natural Science Foundation, China

National Natural Science Fund of China

the Shandong Provincial Medical Health Science and Technology Development Project, China

Publisher

Informa UK Limited

Subject

Obstetrics and Gynaecology,Endocrinology,Endocrinology, Diabetes and Metabolism

Link

Reference19 articles.

Cited by 8 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献