FG syndrome: Report of three new families with linkage to xq12-q22.1

Author:

Graham John M.,Tackels Darci,Dibbern Kurt,Superneau Duane,Rogers Curtis,Corning Ken,Schwartz Charles E.

Publisher

Wiley

Subject

Genetics (clinical)

Cited by 25 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

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4. Broadening the phenotype associated with mutations in UPF3B: Two further cases with renal dysplasia and variable developmental delay;European Journal of Medical Genetics;2012-08

5. Behavioral features in young adults with FG syndrome (Opitz-Kaveggia syndrome);American Journal of Medical Genetics Part C: Seminars in Medical Genetics;2010-10-27

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