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The Journal of Clinical Endocrinology and Metabolism|July 2, 2025
Approach to the patient with a difference of sexual developmentHannes Syryn, Elfride De Baere, Martine CoolsBest Practice & Research. Clinical Endocrinology & Metabolism|April 22, 2019
Update on the genetics of differences of sex development (DSD)Dorien Baetens, Hannah Verdin, Elfride De Baere, et al.Hormone Research in Paediatrics|September 1, 2021
Ovotesticular Difference of Sex Development: Genetic Background, Histological Features, and Clinical ManagementHannes Syryn, Koen Van De Vijver, Martine CoolsHuman Reproduction (Oxford, England)|September 2, 2024
Biallelic RXFP2 variants lead to congenital bilateral cryptorchidism and male infertility, supporting a role of RXFP2 in spermatogenesisHannes Syryn, Julie Van de Velde, Griet De Clercq, et al.European Journal of Pediatrics|April 22, 2025
Role of the pediatrician in the initial management of a newborn with Differences of Sex Development or hypospadiasSaskia van der Straaten, Hannes Syryn, Arianne Dessens, et al.Hormone Research in Paediatrics|January 18, 2012
FOXL2 impairment in human diseaseHannah Verdin, Elfride De BaereClinical Genetics|March 10, 2023
HRAS-related epidermal nevus syndromes: Expansion of the spectrum with first branchial arch defectsAude Beyens, Charlotte Lietaer, Kathleen Claes, et al.Human Mutation|August 30, 2008
FOXL2 mutations and genomic rearrangements in BPESDiane Beysen, Anne De Paepe, Elfride De BaereFolia Histochemica Et Cytobiologica|January 14, 2010
The transcription factor FOXL2 in ovarian function and dysfunctionElfride De Baere, Marc Fellous, Reiner A VeitiaGenetics in Medicine : Official Journal of the American College of Medical Genetics|August 5, 2016
NR5A1 is a novel disease gene for 46,XX testicular and ovotesticular disorders of sex developmentDorien Baetens, Hans Stoop, Frank Peelman, et al.Pageof 33