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Clinical phenotype, gonadal development, and comorbidity spectrum in 43 children with triple X syndrome: a single-center retrospective descriptive case series with cytogenetic refinement in patients with and without X-monosomy-containing cell lines
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@article{{TP}{153979}, author = {Feng, Y., Li, W., Zou, H., Xu, Q., Yang, L.}, title = {Clinical phenotype, gonadal development, and comorbidity spectrum in 43 children with triple X syndrome: a single-center retrospective descriptive case series with cytogenetic refinement in patients with and without X-monosomy-containing cell lines}, journal = {Translational Pediatrics}, volume = {15}, number = {6}, year = {2026}, url = {https://tp.amegroups.org/article/view/153979} }