Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum

M. Castori; D. Castiglia; F. Brancati; M. Foglio; S. Heath; G. Floriddia; S. Madonna; J. Fischer; G. Zambruno

doi:10.1111/j.1399-0004.2010.01513.x

Two families confirm Schöpf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum

M. Castori, D. Castiglia, F. Brancati, M. Foglio, S. Heath, G. Floriddia, S. Madonna, J. Fischer, G. Zambruno

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	92-95
Number of pages	4
Journal	Clinical Genetics
Volume	79
Issue number	1
DOIs	https://doi.org/10.1111/j.1399-0004.2010.01513.x
Publication status	Published - Jan 2011

ASJC Scopus subject areas

Genetics(clinical)
Genetics

Access to Document

10.1111/j.1399-0004.2010.01513.x

Cite this

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title = "Two families confirm Sch{\"o}pf-Schulz-Passarge syndrome as a discrete entity within the WNT10A phenotypic spectrum",

author = "M. Castori and D. Castiglia and F. Brancati and M. Foglio and S. Heath and G. Floriddia and S. Madonna and J. Fischer and G. Zambruno",

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AU - Heath, S.

AU - Floriddia, G.

AU - Madonna, S.

AU - Fischer, J.

AU - Zambruno, G.

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