| Preview | Issue Date | Title | Author(s) | Advisor | Type |
| 2013 | Contribution of polymorphisms in genes associated with craniofacial development to the risk of nonsyndromic cleft lip and/or palate in the Brazilian population | Paranaiba, LMR; de Aquino, SN; Bufalino, A; Martelli, H; Graner, E; Brito, LA; Passos-Bueno, MRDE; Coletta, RD; Swerts, MSO | - | Artigo de periódico |
| 2012 | Cleidocranial dysplasia: oral features and genetic analysis of 11 patients | Bufalino, A; Paranaiba, LMR; Gouvea, AF; Gueiros, LA; Martelli, H; Junior, JJ; Lopes, MA; Graner, E; de Almeida, OP; Vargas, PA; Coletta, RD | - | Artigo de periódico |
| 2011 | A NEWBORN WITH MULTIPLE CONGENITAL ABNORMALITIES OF FACE, GENITALIA, AND EXTREMITIES | Paranaiba, LMR; Martelli, H; Coletta, RD | - | Artigo de periódico |
| 2010 | Maternal Polymorphisms in Folic Acid Metabolic Genes Are Associated with Nonsyndromic Cleft Lip and/or Palate in the Brazilian Population | Bufalino, A; Paranaiba, LMR; de Aquino, SN; Martelli, H; Swerts, MSO; Coletta, RD | - | Artigo de periódico |
| 2010 | Ectrodactyly-Ectodermal Dysplasia-Clefting Syndrome Associated With p63 Mutation and an Uncommon Phenotype | Paranaiba, LMR; Martelli, H; de Miranda, RT; Bufalino, A; Abdo, RC; Coletta, RD | - | Artigo de periódico |
| 2008 | Apert Syndrome: Report of a Case With Emphasis on Craniofacial and Genetic Features | Martelli, H; Paranaiba, LMR; de Miranda, RT; Orsi, J; Coletta, RD | - | Artigo de periódico |
| 2013 | Prevalence of Dental Anomalies in Patients With Nonsyndromic Cleft Lip and/or Palate in a Brazilian Population | Paranaiba, LMR; Coletta, RD; Swerts, MSO; Quintino, RP; de Barros, LM; Martelli, H | - | Artigo de periódico |
| 2016 | Waardenburg syndrome type I: Dental phenotypes and genetic analysis of an extended family | Solia-Nasser, L; de Aquino, SN; Paranaiba, LMR; Gomes, Alexandre; dos-Santos-Neto, P; Coletta, RD; Cardoso, AF; Frota, AC; Martelli-Junior, H | - | Artigo |
| 2010 | Goldenhar syndrome: clinical features with orofacial emphasis | Martelli, H; de Miranda, RT; Fernandes, CM; Bonan, PRF; Paranaiba, LMR; Graner, E; Coletta, RD | - | Artigo de periódico |
| 2013 | Polymorphisms in GABRB3 and Oral Clefting in the Brazilian Population | Filezio, MR; Bagordakis, E; de Aquino, SN; Messetti, ACP; Martelli, H; Swerts, MSO; Graner, E; Coletta, RD; Paranaiba, LMR | - | Artigo de periódico |
| 2013 | Immunoexpression of alpha 2-integrin and Hsp47 in hereditary gingival fibromatosis and gingival fibromatosis-associated dental abnormalities | Vieira, JR; de Oliveira-Santos, C; Della-Coletta, R; Cristianismo-Costa, D; Paranaiba, LMR; Martelli, H | - | Artigo de periódico |
| 2010 | Lack of association between IRF6 polymorphisms (rs2235371 and rs642961) and non-syndromic cleft lip and/or palate in a Brazilian population | Paranaiba, LMR; Bufalino, A; Martelli, H; de Barros, LM; Graner, E; Coletta, RD | - | Artigo de periódico |
| 2008 | Novel mutations in the IRF6 gene in Brazilian families with Van der Woude syndrome | Paranaiba, LMR; Martelli, H; Swerts, MSO; Line, SRP; Coletta, RD | - | Artigo de periódico |
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