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Genotype-phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: Natural history of a patient and review of the literature.
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- American Journal of Medical Genetics. Part A, 2016, v. 170A, n. 3, p. 766, doi. 10.1002/ajmg.a.37494
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A Cytogenomic Approach in a Case of Syndromic XY Gonadal Dysgenesis.
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- Sexual Development, 2016, v. 10, n. 1, p. 23, doi. 10.1159/000444870
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- Article
Implicações diagnosticas de defeitos associados em pacientes com fendas orofaciais típicas.
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- Jornal de Pediatria, 2015, v. 91, n. 5, p. 485, doi. 10.1016/j.jped.2014.12.001
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- Article