D. Moretti-Ferreira

Papers authored by D. Moretti-Ferreira

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2012 Andréa Jeanne Lourenço Nozabieli, Claudia Regina Sgobbi de Faria, Alessandra Rezende Martinelli, Alessandra Madia Mantovani

, C. R. Faria, Dalva Minonroze Albuquerque Ferreira

, Cristina Elena Prado Teles Fregonesi

Análise do equilíbrio postural de indivíduos diabéticos por meio de baropodometria

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George L. Wehby, Norman Goco, Danilo Moretti-Ferreira

, Temis Felix, Antonio Richieri-Costa, Carla Padovani, Fernanda Queiros, Camilla Vila Nova Guimaraes, Camilla Vila Nova Guimaraes, Guimaraes Rui Pereira, Steve Litavecz, Tyler Hartwell, Hrishikesh Chakraborty

, Lorette Javois, Jeffrey C. Murray

Oral cleft prevention program (OCPP)

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Marcelo Razera Baruffi, Deise Helena de Souza, Rosana Aparecida Bicudo da Silva, Ester Silveira Ramos, Danilo Moretti-Ferreira

Autism Spectrum Disorder in a Girl with aDe NovoX;19 Balanced Translocation

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2011 Lamônica,Dionísia Aparecida Cusin, Greyce Kelly da Silva, Dionísia Aparecida Cusin Lamônica, Greyce Kelly da Silva, Silva,Greyce Kelly Da, Renata Heloísa Furlan, Furlan,Renata Heloísa, Dagma Venturini Marques Abramides, Gustavo Henrique Vieira, Abramides,Dagma Venturini Marques, Vieira,Gustavo Henrique, Danilo Moretti-Ferreira

, Célia Maria Giacheti, Giacheti,Célia Maria

Características clínicas, comportamentais, cognitivas e comunicativa na síndrome Smith-Magenis

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Gustavo H. Vieira, Jayson D. Rodriguez, Paulina Carmona-Mora

, Lei Cao, Bruno F. Gamba, Daniel R. Carvalho, Andréa de Rezende Duarte, Andréa de Rezende Duarte, Suely R. Santos, Deise H. de Souza, Deise H. de Souza, Barbara R. DuPont, Katherina Walz, Danilo Moretti-Ferreira

, Anand K. Srivastava

Detection of classical 17p11.2 deletions, an atypical deletion and RAI1 alterations in patients with features suggestive of Smith–Magenis syndrome

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Nicholas K. Rorick, Akira Kinoshita, Jason L. Weirather, Myriam Peyrard-Janvid, Renata L. L. Ferreira de Lima, Renata L. L. Ferreira de Lima, Martine Dunnwald, Alan L. Shanske, Danilo Moretti-Ferreira

, Hannele Koillinen, Juha Kere, Maria A. Mansilla, Jeffrey C. Murray, Steve L. Goudy, Brian C. Schutte

Genomic Strategy Identifies a Missense Mutation in WD-Repeat Domain 65 (WDR65) in an Individual with Van der Woude Syndrome

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Gustavo H. Vieira, Jayson D. Rodriguez, Raquel Boy, Isaias Soares de Paiva, Isaias Soares de Paiva, Barbara R. Dupont, Danilo Moretti-Ferreira

, Anand K. Srivastava

Differential diagnosis of Smith-Magenis syndrome: 1p36 deletion syndrome

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Changsoo Kang, Bianca Santos Domingues, Eduardo Sainz, Carlos Eduardo Frigério Domingues, Carlos Eduardo Frigerio Domingues, Dennis Drayna, Danilo Moretti-Ferreira

Evaluation of the association between polymorphisms at the DRD2 locus and stuttering

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Regina Helena Garcia Martins

, Tm M. Goncalves, Ds S. Neves, Ta A. Fracalossi, Fracalossi Ta, Elm L. M. Tavares, D. Moretti-Ferreira

Sulcus vocalis: evidence for autosomal dominant inheritance

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B. F. Gamba, G. H. Vieira, D. H. Souza, F. F. Monteiro, J. J. Lorenzini, D. R. Carvalho, D. Morreti-Ferreira

Smith-Magenis syndrome: clinical evaluation in seven Brazilian patients

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2009 Jane W. Kimani, Koh-Ichiro Yoshiura, Min Shi, Astanand Jugessur, Danilo Moretti-Ferreira

, Kaare Christensen, Jeffrey C. Murray

Search for Genomic Alterations in Monozygotic Twins Discordant for Cleft Lip And/Or Palate

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Rossi,Natalia Freitas, Natalia Freitas Rossi, Deise Helena de Souza, Souza,Deise Helena De, Danilo Moretti-Ferreira

, Célia Maria Giacheti, Giacheti,Célia Maria

Perfil da fluência da fala na síndrome de Williams-Beuren: estudo preliminar

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N. F. Rossi, A. R. Gatto, P. C. Cola, D. H. Souza, D. Moretti-Ferreira

, C. M. Giacheti

Case Report Oropharyngeal dysphagia and language delay in partial trisomy 9p: case report

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Renata L. L. Ferreira de Lima, Renata L. L. Ferreira de Lima, Renata L. L. Ferreira de Lima, Sarah A. Hoper, Michella Ghassibé

, Margaret E. Cooper, Nicholas K. Rorick, Shinji Kondo, Lori Katz, Mary L. Marazita, John Compton, Sherri Bale, Ute Hehr, Michael J. Dixon, Sandra Daack-Hirsch and 11 other authors

Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syndrome.

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2008 Daniel Rocha de Carvalho, Daniel Rocha de Carvalho, Natalia Freitas Rossi, Silvana Artioli Schellini, Danilo Moretti-Ferreira

, Antonio Richieri-Costa

Schilbach-Rott/blepharofacioskeletal syndrome in a Brazilian patient

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C. T. Giunco, D. Moretti-Ferreira

, A. E. Silva, S. S. Rocha, A. C. Fett-Conte

MOMO syndrome associated with autism: a case report

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D. Moretti-Ferreira

Macrossomia e habilidades neuropsicolingüísticas

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D. Moretti-Ferreira

Atuação fonoaudiológica no serviço de aconselhamento genético: relato de experiência.

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2007 Martins,Regina Helena Garcia, Silva,Rafael, Regina Helena Garcia Martins, Rafael Silva, Danilo Moretti Ferreira

, Ferreira,Danilo Moretti, Norimar Hernandes Dias, Dias,Norimar Hernandes

Sulco vocal: provável etiologia genética. Relato de quatro casos em familiares

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Natalia Freitas Rossi, Danilo Moretti-Ferreira

, Célia Maria Giacheti

Perfil comunicativo de indivíduos com a síndrome de Williams-Beuren

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Papers authored by D. Moretti-Ferreira