Associated Papers
Expanding the clinical and molecular spectrum of TBC1D32-related ciliopathy: case reports and literature Review.
Eiumtrakul W et al.
Journal of Human Genetics, 2025
Contribution of rare coding variants to microcephaly in individuals with neurodevelopmental disorders.
Yoon JG et al.
Genome Medicine, 2025
40770811 (PubMed )
Supplement: 13073_2025_1513_MOESM2_ESM.xlsx › ST3
Clinical and genetic features of childhood-onset congenital combined pituitary hormone deficiency: a retrospective, single-center cohort study.
Lee Y et al.
Annals of Pediatric Endocrinology & Metabolism, 2024
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