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Spleen function is reduced in individuals with NR5A1 variants with or without a difference of sex development : a cross-sectional study
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Individuals with NR5A1 (SF1) mutations and atypical sex development and their asymptomatic family member carriers are at high risk of hyposplenism
(2021) HORMONE RESEARCH IN PAEDIATRICS. In Hormone Research in Paediatrics 94(supplement 1). p.42-43 -
Diagnostiek bij disorders/differences of sex development (dsd)
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Complete androgen insensitivity syndrome: factors influencing gonadal histology including germ cell pathology
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Advanced pubertal development in two adolescents with new SF-1 mutations