Sequence variant in the CDC42BPB gene is potentially associated with Mullerian duct anomalies-Reference-Cited by-同舟云学术

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Sequence variant in the CDC42BPB gene is potentially associated with Mullerian duct anomalies

Published:2020-02-10 Issue:5 Volume:46 Page:684-693
ISSN:1341-8076
Container-title:Journal of Obstetrics and Gynaecology Research
language:en
Short-container-title:J. Obstet. Gynaecol. Res.

Author:

Luo Li‐Jing¹,Feng Fan²,Li Sheng‐Hui¹,Lu Dan¹,Li Lin³^ORCID,Zhou Qi¹

Affiliation:

1. Department of GynecologyBeijing Obstetrics and Gynecology Hospital, Capital Medical University Beijing China

2. Department of Basic Medical SciencesSchool of Medicine, Tsinghua University Beijing China

3. Central LaboratoryBeijing Obstetrics and Gynecology Hospital, Capital Medical University Beijing China

Funder

Beijing Obstetrics and Gynecology Hospital, Capital Medical University

Publisher

Wiley

Subject

Obstetrics and Gynaecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jog.14211

Reference41 articles.

1. The ESHRE/ESGE consensus on the classification of female genital tract congenital anomalies

2. Estimated Prevalence of Müllerian Anomalies

3. Incidence of Mullerian defects in fertile and infertile women

4. Heritable aspects of uterine anomalies. I. Three familial aggregates with Müllerian fusion anomalies**Supported in part by NIH grants HD 11021 and HD 02841, and grants from the March of Dimes.

5. Three sisters with septate uteri: another reference to bidirectional theory

Cited by 1 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

1. Studying Müllerian duct anomalies – from cataloguing phenotypes to discovering causation;Disease Models & Mechanisms;2021-06-01

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