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PARK2 Microduplication: Clinical and Molecular Characterization of a Further Case and Review of the Literature.
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- Molecular Syndromology, 2016, v. 7, n. 5, p. 282, doi. 10.1159/000448852
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Clinical and molecular characterization of an emerging chromosome 22q13.31 microdeletion syndrome.
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- American Journal of Medical Genetics. Part A, 2018, v. 176, n. 2, p. 391, doi. 10.1002/ajmg.a.38559
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- Article
Long QT syndrome in chromosome 7q35q36.3 deletion involving KCNH2 gene: Warning for chlorpheniramine prescription.
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- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 9, p. N.PAG, doi. 10.1002/mgg3.855
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- Article