A female infant with Frasier syndrome showing splice site mutation in Wilms' tumor gene (WT1) intron 9.
Fujita S; Sugimoto K; Miyazawa T; Yanagida H; Tabata N; Okada M; Takemura T; Clinical Nephrology, 2010, vol. 73, issue 6, p 487, ISSN 03010430. ISBN 03010430.

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