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An N-terminal WT1 mutation (P181S) in an XY patient with ambiguous genitalia, normal testosterone production, absence of kidney disease and associated heart defect: enlarging the phenotypic spectrum of WT1 defects by Kohler, B; Pienkowski, C; Audran, F; Delsol, M; Tauber, M; Paris, F; Sultan, C; Lumbroso, S is a Medicine article available to read on EtoBox.

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Author
Kohler, B; Pienkowski, C; Audran, F; Delsol, M; Tauber, M; Paris, F; Sultan, C; Lumbroso, S
Publisher
Bioscientifica; BioScientifica Ltd. (ISSN 0804-4643)
Published
2004
Language
EN
Field
Medicine (Health Sciences)

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