A multi-exon deletion within WWOX is associated with a 46,XY disorder of sex development

Copy Number Variation in Patients with Disorders of Sex Development Due to 46,XY Gonadal Dysgenesis

(2011) Stefan White et al.   PLoS One

Gonadal Development and Tumor Formation at the Crossroads of Male and Female Sex Determination

(2011) M. Cools et al.   Sexual Development

Identification of SOX3 as an XX male sex reversal gene in mice and humans

(2010) Edwina Sutton et al.   JOURNAL OF CLINICAL INVESTIGATION

Copy number variation and mosaicism

(2009) A.J. Notini et al.   CYTOGENETIC AND GENOME RESEARCH

WWOX: Its genomics, partners, and functions

(2009) Sara Del Mare et al.   JOURNAL OF CELLULAR BIOCHEMISTRY

Inhibition of the Wnt/β-catenin pathway by the WWOX tumor suppressor protein

(2009) N Bouteille et al.   ONCOGENE

Targeted Ablation of the WW Domain-Containing Oxidoreductase Tumor Suppressor Leads to Impaired Steroidogenesis

(2008) Rami I. Aqeilan et al.   ENDOCRINOLOGY

Stabilization of β-catenin in XY gonads causes male-to-female sex-reversal

(2008) Danielle M. Maatouk et al.   HUMAN MOLECULAR GENETICS

Stem cell factor as a novel diagnostic marker for early malignant germ cells

(2008) H Stoop et al.   JOURNAL OF PATHOLOGY

FOXL2 and SOX9 as parameters of female and male gonadal differentiation in patients with various forms of disorders of sex development (DSD)

(2008) R Hersmus et al.   JOURNAL OF PATHOLOGY