Medical sequencing of candidate genes for nonsyndromic cleft lip and palate von Vieira, Alexandre R, Avila, Joseph R, Daack-Hirsch, Sandra, Dragan, Ecaterina, Félix, Têmis M, Rahimov, Fedik, Harrington, Jill, Schultz, Rebecca R, Watanabe, Yoriko, Johnson, Marla, Fang, Jennifer, O'Brien, Sarah E, Orioli, Iêda M, Castilla, Eduardo E, Fitzpatrick, David R, Jiang, Rulang, Marazita, Mary L, Murray, Jeffrey C

Volltext

Author Correction: Dental anomaly detection using intraoral photos via deep learning von Ragodos, Ronilo, Wang, Tong, Padilla, Carmencita, Hecht, Jacqueline T., Poletta, Fernando A., Orioli, Iêda M., Buxó, Carmen J., Butali, Azeez, Valencia-Ramirez, Consuelo, Muñeton, Claudia Restrepo, Wehby, George L., Weinberg, Seth M., Marazita, Mary L., Moreno Uribe, Lina M., Howe, Brian J.

Volltext

ECLAMC: The Latin-American Collaborative Study of Congenital Malformations von Castilla, Eduardo E., Orioli, Iêda M.

Volltext

A large, ten‐generation family with autosomal dominant preaxial polydactyly/triphalangeal thumb: Historical, clinical, genealogical, and molecular studies von Álvarez, Luis Francisco González, Tenorio‐Castaño, Jair, Poletta, Fernando A., Santos‐Simarro, Fernando, Arias, Pedro, Gallego, Natalia, Orioli, Iêda Maria, Mundlos, Stefan, Castilla, Eduardo E., Martínez‐Glez, Víctor, Martínez‐Frías, María Luisa, Ruiz‐Pérez, Víctor L., Nevado, Julián, Lapunzina, Pablo

Volltext

Individuals with nonsyndromic orofacial clefts have increased asymmetry of fingerprint patterns von Neiswanger, Katherine, Mukhopadhyay, Nandita, Rajagopalan, Shwetha, Leslie, Elizabeth J, Sanchez, Carla A, Hecht, Jacqueline T, Orioli, Iêda M, Poletta, Fernando A, de Salamanca, Javier Enríquez, Weinberg, Seth M, Marazita, Mary L

Volltext

Dental anomaly detection using intraoral photos via deep learning von Ragodos, Ronilo, Wang, Tong, Padilla, Carmencita, Hecht, Jacqueline T., Poletta, Fernando A., Orioli, Iêda M., Buxó, Carmen J., Butali, Azeez, Valencia-Ramirez, Consuelo, Restrepo Muñeton, Claudia, Wehby, George L., Weinberg, Seth M., Marazita, Mary L., Moreno Uribe, Lina M., Howe, Brian J.

Volltext

Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay von Weber, Megan L, Hsin, Hong-Yuan, Kalay, Ersan, BroŽková, Dana S, Shimizu, Takehiko, Bayram, Merve, Deeley, Kathleen, Küchler, Erika C, Forella, Jessalyn, Ruff, Timothy D, Trombetta, Vanessa M, Sencak, Regina C, Hummel, Michael, Briseño-Ruiz, Jessica, Revu, Shankar K, Granjeiro, José M, Antunes, Leonardo S, Antunes, Livia A, Abreu, Fernanda V, Costa, Marcelo C, Tannure, Patricia N, Koruyucu, Mine, Patir, Asli, Poletta, Fernando A, Mereb, Juan C, Castilla, Eduardo E, Orioli, Iêda M, Marazita, Mary L, Ouyang, Hongjiao, Jayaraman, Thottala, Seymen, Figen, Vieira, Alexandre R

Volltext

Association of methylenetetrahydrofolate reductase gene 677C > T polymorphism and Down syndrome von Costa-Lima, Marcelo Aguiar, Amorim, Márcia Rodrigues, Orioli, Iêda Maria

Volltext

Folic acid flour fortification: Impact on the frequencies of 52 congenital anomaly types in three South American countries von López-Camelo, Jorge S., Castilla, Eduardo E., Orioli, Iêda M.

Volltext

Prevalence and clinical profile of microcephaly in South America pre-Zika, 2005-14: prevalence and case-control study von Orioli, Iêda M, Dolk, Helen, Lopez-Camelo, Jorge S, Mattos, Daniel, Poletta, Fernando A, Dutra, Maria G, Carvalho, Flavia M, Castilla, Eduardo E

Volltext

Prenatal Diagnosis of Skeletal Dysplasias: Contribution of Three-Dimensional Computed Tomography von Ulla, Marina, Aiello, Horacio, Cobos, María Paz, Orioli, Iêda, García-Mónaco, Ricardo, Etchegaray, Adolfo, Igarzábal, María Laura, Otaño, Lucas

Volltext

New SHH and Known SIX3 Variants in a Series of Latin American Patients with Holoprosencephaly von de Castro, Viviane Freitas, Mattos, Daniel, de Carvalho, Flavia Martinez, Cavalcanti, Denise Pontes, Duenas-Roque, Milagros M., Llerena Jr, Juan, Cosentino, Viviana Raquel, Honjo, Rachel Sayuri, Leite, Julio Cesar Loguercio, Sanseverino, Maria Teresa, de Souza, Márcia Pereira Alves, Bernardi, Pricila, Bolognese, Ana Maria, Santana da Silva, Luiz Carlos, Barbero, Pablo, Correia, Patricia Santana, Bueno, Larissa Souza Mario, Savastano, Clarice Pagani, Orioli, Iêda Maria

Volltext

Preliminary data on changes in neural tube defect prevalence rates after folic acid fortification in South America von Castilla, Eduardo E., Orioli, Iêda M., Lopez-Camelo, Jorge S., Dutra, Maria da Graça, Nazer-Herrera, Julio

Volltext

Effects of folic acid fortification on spina bifida prevalence in Brazil von Orioli, Iêda Maria, Lima do Nascimento, Ricardo, López-Camelo, Jorge Santiago, Castilla, Eduardo Enrique

Volltext

Enamel formation genes influence enamel microhardness before and after cariogenic challenge von Shimizu, Takehiko, Ho, Bao, Deeley, Kathleen, Briseño-Ruiz, Jessica, Faraco, Jr, Italo M, Schupack, Brett I, Brancher, João A, Pecharki, Giovana D, Küchler, Erika C, Tannure, Patricia N, Lips, Andrea, Vieira, Thays C S, Patir, Asli, Yildirim, Mine, Poletta, Fernando A, Mereb, Juan C, Resick, Judith M, Brandon, Carla A, Orioli, Iêda M, Castilla, Eduardo E, Marazita, Mary L, Seymen, Figen, Costa, Marcelo C, Granjeiro, José M, Trevilatto, Paula C, Vieira, Alexandre R

Volltext

A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13 von Leslie, Elizabeth J, Carlson, Jenna C, Shaffer, John R, Feingold, Eleanor, Wehby, George, Laurie, Cecelia A, Jain, Deepti, Laurie, Cathy C, Doheny, Kimberly F, McHenry, Toby, Resick, Judith, Sanchez, Carla, Jacobs, Jennifer, Emanuele, Beth, Vieira, Alexandre R, Neiswanger, Katherine, Lidral, Andrew C, Valencia-Ramirez, Luz Consuelo, Lopez-Palacio, Ana Maria, Valencia, Dora Rivera, Arcos-Burgos, Mauricio, Czeizel, Andrew E, Field, L Leigh, Padilla, Carmencita D, Cutiongco-de la Paz, Eva Maria C, Deleyiannis, Frederic, Christensen, Kaare, Munger, Ronald G, Lie, Rolv T, Wilcox, Allen, Romitti, Paul A, Castilla, Eduardo E, Mereb, Juan C, Poletta, Fernando A, Orioli, Iêda M, Carvalho, Flavia M, Hecht, Jacqueline T, Blanton, Susan H, Buxó, Carmen J, Butali, Azeez, Mossey, Peter A, Adeyemo, Wasiu L, James, Olutayo, Braimah, Ramat O, Aregbesola, Babatunde S, Eshete, Mekonen A, Abate, Fikre, Koruyucu, Mine, Seymen, Figen, Ma, Lian, de Salamanca, Javier Enríquez, Weinberg, Seth M, Moreno, Lina, Murray, Jeffrey C, Marazita, Mary L

Volltext

Clinical epidemiology of skeletal dysplasias in South America von Barbosa-Buck, Cecília O., Orioli, Iêda M., da Graça Dutra, Maria, Lopez-Camelo, Jorge, Castilla, Eduardo E., Cavalcanti, Denise P.

Volltext

Aquaporin 5 Interacts with Fluoride and Possibly Protects against Caries von Anjomshoaa, Ida, Briseño-Ruiz, Jessica, Deeley, Kathleen, Poletta, Fernardo A, Mereb, Juan C, Leite, Aline L, Barreta, Priscila A T M, Silva, Thelma L, Dizak, Piper, Ruff, Timothy, Patir, Asli, Koruyucu, Mine, Abbasoğlu, Zerrin, Casado, Priscila L, Brown, Andrew, Zaky, Samer H, Bayram, Merve, Küchler, Erika C, Cooper, Margaret E, Liu, Kai, Marazita, Mary L, Tanboğa, İlknur, Granjeiro, José M, Seymen, Figen, Castilla, Eduardo E, Orioli, Iêda M, Sfeir, Charles, Owyang, Hongjiao, Buzalaf, Marília A R, Vieira, Alexandre R

Volltext

Rare nasal cleft in a patient with holoprosencephaly due to a mutation in the ZIC2 gene von Savastano, Clarice Pagani, Bernardi, Pricila, Seuánez, Hector N., Moreira, Miguel Ângelo Martins, Orioli, Iêda Maria

Volltext

Mothers of children with Down syndrome: a clinical and epidemiological study von Aprigio, Joissy, de Castro, Carolina M. L., Lima, Marcelo A. Costa, Ribeiro, Márcia G., Orioli, Iêda M., Amorim, Márcia R.

Volltext