Phenotypic heterogeneity in 22q11.2 deletion syndrome: Copy Number Variants as genetic modifiers for congenital heart disease in a Brazilian cohort by Zamariolli, M., Dantas, A. G., Nunes, N., Moysés‐Oliveira, M., Sgardioli, I. C., Soares, D. C. Q., Gil‐Da‐Silva‐Lopes, V. L., Kim, C. A., Melaragno, M. I.

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Phenotype comparison among individuals with developmental delay/intellectual disability with or without genomic imbalances by Souza, L. C., Santos, A. P., Sgardioli, I. C., Viguetti‐Campos, N. L., Marques Prota, J. R., Oliveira‐Sobrinho, R. P., Vieira, T. P., Gil‐da‐Silva‐Lopes, V. L.

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Study of IRF6 and 8q24 region in non-syndromic oral clefts in the Brazilian population by de Souza, LT, Kowalski, TW, Ferrari, J, Monlléo, IL, Ribeiro, EM, de Souza, J, Fett-Conte, AC, de Araujo, TK, Gil-da-Silva-Lopes, VL, Ribeiro-dos-Santos, ÂKC, dos Santos, SEB, Félix, TM

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Investigation of the 22q11.2 candidate region in patients with midline facial defects with hypertelorism by Simioni, M., Freitas, É. Lopes, Vieira, T. Paiva, Lopes-Cendes, I., Gil-da-Silva-Lopes, V. Lúcia

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Central nervous system abnormalities on midline facial defects with hypertelorism detected by magnetic resonance image and computed tomography by Gil-da-Silva-Lopes, Vera Lúcia, Giffoni, Silvio David Araújo

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A clinical study of 31 individuals with midline facial defects with hypertelorism and a guideline for follow-up by Gil-da-Silva-Lopes, Vera Lúcia, Maciel-Guerra, Andréa Trevas

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Congenital Temporomandibular Joint Ankylosis: Clinical Characterization and Natural History of Four Unrelated Affected Individuals by Gil-da-Silva-Lopes, Vera Lúcia, Luquetti, Daniela Varela

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Q289P Mutation in FGFR2 Gene Causes Saethre-Chotzen Syndrome: Some Considerations About Familial Heterogeneity by de Freitas, Érika Cristina Lopes Burrone, Nascimento, Sandra Regina Dantas, de Mello, Maricilda Palandi, Gil-da-Silva-Lopes, Vera Lúcia

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Study of IRF 6 and 8q24 region in non‐syndromic oral clefts in the Brazilian population by de Souza, LT, Kowalski, TW, Ferrari, J, Monlléo, IL, Ribeiro, EM, de Souza, J, Fett‐Conte, AC, de Araujo, TK, Gil‐da‐Silva‐Lopes, VL, Ribeiro‐dos‐Santos, ÂKC, dos Santos, SEB, Félix, TM

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Ohdo syndrome: report on a Brazilian girl with additional findings by Lopes, Vera Lúcia Gil da Silva, Guion‐Almeida, Maria Leine

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A dup(17)(p11.2p11.2) detected by fluorescence in situ hybridization in a boy with Alport syndrome by Balarin, Marly Aparecida Spadotto, Lopes, Vera Lúcia Gil da Silva, Varella-Garcia, Marileila

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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 by Fontes, Marshall I. B., Santos, Ana P., Molck, Miriam C., Simioni, Milena, Nascimento, Diogo L. L., Andrade, Ana K. M., Rosenberg, Carla, Krepischi, Ana C. V., Appenzeller, Simone, Monlleó, Isabella L., Gil-da-Silva-Lopes, Vera Lúcia

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