An association of 19p13.2 microdeletions with Malan syndrome and Chiari malformation-Reference-Cited by-同舟云学术

An association of 19p13.2 microdeletions with Malan syndrome and Chiari malformation

Author:

Shimojima Keiko¹²,Okamoto Nobuhiko³,Tamasaki Akiko⁴,Sangu Noriko²⁵,Shimada Shino²⁶,Yamamoto Toshiyuki²

Affiliation:

1. Precursory Research for Embryonic Science and Technology (PRESTO); Japan Science and Technology Agency (JST); Kawaguchi Japan

2. Tokyo Women's Medical University Institute for Integrated Medical Sciences; Tokyo Japan

3. Department of Medical Genetics; Osaka Medical Center and Research Institute for Maternal and Child Health; Osaka Japan

4. Division of Child Neurology; Tottori University; Tottori Japan

5. Department of Dental surgery; Tokyo Women's Medical University; Tokyo Japan

6. Department of Pediatrics; Tokyo Women's Medical University; Tokyo Japan

Funder

grant from the Japan Epilepsy Research Foundation (JERF)

grant from the Kanae Foundation for the promotion of Medical Science in Japan (KS)

Grant-in-Aid for Scientific Research from Health Labor Sciences Research Grants from the Ministry of Health

Grant-in-Aid for Young Scientists (B), from the Japan Society for the Promotion of Science (JSPS)

Precursory Research for Embryonic Science and Technology (PRESTO) grant), from the Japan Science and Technology Agency (JST)

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

Reference20 articles.

Cited by 17 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