A novel mutation of HOXA11 in a patient with septate uterus-Reference-Cited by-同舟云学术

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A novel mutation of HOXA11 in a patient with septate uterus

Published:2017-12 Issue:1 Volume:12 Page:
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet J Rare Dis

Author:

Zhu Ying,Cheng Zhi,Wang Jing,Liu Beihong,Cheng Longfei,Chen Beili,Cao Yunxia,Wang Binbin

Funder

National Natural Science Foundation of China

central government special funds to guide the development of local science and technology

National Infrastructure of Chinese Genetic Resources

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics (clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13023-017-0727-9.pdf

Reference38 articles.

1. Kobayashi A, Behringer RR. Developmental genetics of the female reproductive tract in mammals. Nat Rev Genet. 2003;4:969–80.

2. Chan YY, Jayaprakasan K, Zamora J, Thornton JG, Raine-Fenning N, Coomarasamy A. The prevalence of congenital uterine anomalies in unselected and high-risk populations: a systematic review. Hum Reprod Update. 2011;17:761–71.

3. Li S, Qayyum A, Coakley FV, Hricak H. Association of renal agenesis and mullerian duct anomalies. J Comput Assist Tomogr. 2000;24:829–34.

4. Golan A, Langer R, Bukovsky I, Caspi E. Congenital anomalies of the mullerian system. Fertil Steril. 1989;51:747–55.

5. Vallerie AM, Breech LL. Update in Mullerian anomalies: diagnosis, management, and outcomes. Current opinion in obstetrics & gynecology. 2010;22:381–7.

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