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Novel molecular, structural and clinical findings in an Italian cohort of congenital cataract.
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- Clinical Genetics, 2024, v. 106, n. 4, p. 403, doi. 10.1111/cge.14568
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Identification of bi‐allelic LFNG variants in three patients and further clinical and molecular refinement of spondylocostal dysostosis 3.
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- Clinical Genetics, 2023, v. 104, n. 2, p. 230, doi. 10.1111/cge.14336
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- Article