Clinical and genetic characteristics of rare congenital adrenal hyperplasia: a retrospective analysis in a Chinese population. [PDF]
Chan K, Guo Y, Zhang S, Yan L.
europepmc +1 more source
Prevalence of Differences of Sex Development Among Pediatric Endocrine Care Centers in Switzerland From 2000 to 2019. [PDF]
Metzger S +19 more
europepmc +1 more source
Splenic structural and functional abnormalities in individuals with NR5A1/SF-1 variants. [PDF]
Fouatih K +18 more
europepmc +1 more source
Sex chromosome-dependent epigenetic regulation underlies sex-specific H4 acetylation at the aromatase promoter in the developing mouse amygdala. [PDF]
Sosa C +4 more
europepmc +1 more source
When Lifelong Anosmia Reveals Hypogonadism: A Case of Kallmann Syndrome with Primary Amenorrhea. [PDF]
Lubis JYG +3 more
europepmc +1 more source
Clinical Spectrum, Surgical Management, and Outcomes of <i>NR5A1</i>-Related 46,XY Differences of Sex Development: A Narrative Review. [PDF]
Vicario S +6 more
europepmc +1 more source
Embryonic origin of XX/XY chimerism in an in vitro fertilization-conceived individual. [PDF]
Patel A +3 more
europepmc +1 more source
Integrative Bioinformatics Analyses Reveal X Chromosome Inactivation Escape Genes Dosage Dysregulation Is the Primary Contributor to Turner Syndrome. [PDF]
Liang H, Li Z, Zhang F.
europepmc +1 more source
Clinical Presentation and Management of Swyer Syndrome: A Case Report. [PDF]
Errahali Y +4 more
europepmc +1 more source

