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Syndromic Oral Clefts: Challenges of Genetic Assessment in Brazil and Suggestions to Improve Health Policies.
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- Public Health Genomics, 2019, v. 22, n. 1/2, p. 69, doi. 10.1159/000501973
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- Article
Genomic Investigation of Balanced Chromosomal Rearrangements in Patients with Abnormal Phenotypes.
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- Molecular Syndromology, 2017, v. 8, n. 4, p. 187, doi. 10.1159/000477084
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- Article
17p13.3 Microdeletion: Insights on Genotype-Phenotype Correlation.
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- Molecular Syndromology, 2017, v. 8, n. 1, p. 36, doi. 10.1159/000452753
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- Article
22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity.
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- Genes, 2024, v. 15, n. 4, p. 518, doi. 10.3390/genes15040518
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- Article
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
Local Strategies to Address Health Needs of Individuals With Orofacial Clefts in Alagoas, Brazil.
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- Cleft Palate Craniofacial Journal, 2013, v. 50, n. 4, p. 424, doi. 10.1597/11-069
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- Article
Implementing the Brazilian Database on Orofacial Clefts.
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- Plastic Surgery International, 2013, p. 1, doi. 10.1155/2013/641570
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- Article
Preliminary Analysis of the Nonsynonymous Polymorphism rs17563 in BMP4 Gene in Brazilian Population Suggests Protection for Nonsyndromic Cleft Lip and Palate.
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- Plastic Surgery International, 2012, p. 1, doi. 10.1155/2012/247104
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- Article
Brazil's Craniofacial Project: Different approaches on orofacial clefts and 22q11.2 deletion syndrome.
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- American Journal of Medical Genetics. Part C: Seminars in Medical Genetics, 2020, v. 184, n. 4, p. 912, doi. 10.1002/ajmg.c.31852
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- Article
Profile of patients with genitourinary anomalies treated in a clinical genetics service in the Brazilian unified health system.
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- Revista Paulista de Pediatria, 2016, v. 34, n. 1, p. 91, doi. 10.1016/j.rppede.2015.06.024
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- Article
Distúrbios da Diferenciação do Sexo: da diferença anatômica à diferença psíquica.
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- Gerais: Revista Interinstitucional de Psicologia, 2021, v. 14, n. 3, p. 1, doi. 10.36298/gerais202114e16849
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- Article
Functional characterization of five NR5A1 gene mutations found in patients with 46,XY disorders of sex development.
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- Human Mutation, 2018, v. 39, n. 1, p. 114, doi. 10.1002/humu.23353
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- Article