Molecular Analysis of Frasier Syndrome: Mutation in the WT1 Gene in a Girl with Gonadal Dysgenesis and Nephronophthisis

Article

G. Perez de Nanclares, , L. Castaño, , J R. Bilbao, , A. Vallo, , I. Rica, , A. Vela, and P. Martul,

Published/Copyright: July 1, 2002

Published by

Become an author with De Gruyter Brill

Submit Manuscript Author Information Explore this Subject

Published Online: 2002-07

You are currently not able to access this content.

Institutional Access

How does access work?

Winner of the OpenAthens UX Award 2026

Have an idea on how to improve our website?

Please write us.

Downloaded on 6.3.2026 from https://www.degruyterbrill.com/document/doi/10.1515/JPEM.2002.15.7.1047/html