Kokitsu-Nakata Nancy Mizue - Hospital for Rehabilitation of Craniofacial Anomalies, University of São Paulo

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论文共 59 篇作者统计合作学者相似作者

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Hemiarhinia Caused by a Missense Variation in SMCHD1: A Mild Phenotype in the Clinical Spectrum of Bosma Arhinia Microphthalmia Syndrome

Nancy Mizue Kokitsu-Nakata, Vinicius Contrucci Dantas Segarra,Cristiano Tonello,Michele Madeira Brandao,Nivaldo Alonso,Roseli Maria Zechi-Ceide

American journal of medical genetics Part Ano. 10 (2024): e63640-e63640

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Low-pass Whole Genome Sequencing As a Cost-Effective Alternative to Chromosomal Microarray Analysis for Low- and Middle-Income Countries

Patricia C. Mazzonetto,Darine Villela,Ana C. V. Krepischi,Paulo M. Pierry,Adriano Bonaldi,Luiz Gustavo D. Almeida,Marcelo G. Paula, Matheus Carvalho Burger, Ana Gabriela de Oliveira, Gustavo G. G. Fonseca, Roberto Giugliani, Mariluce Riegel-Giugliani,Debora Bertola,Guilherme Lopes Yamamoto,Maria Rita Passos-Bueno,Gabriele da Silva Campos, Ana Claudia Dantas Machado,Juliana F. Mazzeu,Eduardo Perrone,Roseli M. Zechi-Ceide,Nancy M. Kokitsu-Nakata,Tarsis Paiva Vieira,Carlos Eduardo Steiner,Vera Lucia Gil-da-Silva-Lopes, Daniela Koeller Rodrigues Vieira,Raquel Boy, Joao Monteiro de Pina-Neto,Cristovam Scapulatempo-Neto,Fernanda Milanezi,Carla Rosenberg

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2024)

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Monodactyly in a Patient with CHARGE Syndrome: an Additional Case Report

Henrique Regonaschi Serigatto,Roseli Maria Zechi-Ceide, Isabella Parizotto,Nancy Mizue Kokitsu-Nakata

AMERICAN JOURNAL OF MEDICAL GENETICS PART Ano. 6 (2024)

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Identification of a De Novo PUF60 Variant Associated with Craniofacial Microsomia

Takuya Ogawa,Jingyi Xue,Long Guo,Maristela Sayuri Inoue-Arai,Siulan Vendramini-Pittoli,Roseli Maria Zechi-Ceide,Rosana Maria Candido-Souza,Cristiano Tonello,Michele Madeira Brandao,Terumi Okada Ozawa,Adriano Porto Peixoto, Daniela Maria Cury Ferreira Ruiz,Tomoki Nakashima,Shiro Ikegawa,Keiji Moriyama,Nancy Mizue Kokitsu-Nakata

AMERICAN JOURNAL OF MEDICAL GENETICS PART A（2024）

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Systemic and Oral Abnormalities in Kabuki Syndrome: a Case Series

Lidiane Castro Pinto,Nancy Mizue Kokitsu-Nakata,Gisele da Silva Dalben,Lucas Jose de Azevedo Silva,Ana Lucia Pompe Fraga de Almeida

Oral surgery, oral medicine, oral pathology and oral radiologyno. 5 (2024): e91-e98

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Complex Craniofacial Cleft and Accessory Maxilla in Oculoauriculofrontonasal Syndrome

Henrique R. Serigatto,Nancy M. Kokitsu-Nakata,Priscila P. Moura,Siulan Vendramini-Pittoli,Luiza A. Virmond,Adriano P. Peixoto,Cristiano Tonello,Luciano A. Brito,Maria R. Passos-Bueno,Roseli M. Zechi-Ceide

CLINICAL DYSMORPHOLOGY（2023）

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Oculoauriculofrontonasal Syndrome: Refining the Phenotype Through a New Case Series and Literature Review

Henrique Regonaschi Serigatto,Nancy Mizue Kokitsu‐Nakata,Siulan Vendramini‐Pittoli,Cristiano Tonello,Priscila Padilha Moura,Adriano Porto Peixoto,Luiz Paulo Gomes,Roseli Maria Zechi‐Ceide

American Journal of Medical Genetics Part Ano. 10 (2023): 2493-2507

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Clinical and radiological aspects of 34 Brazilian individuals with oculoauriculofrontonasal syndrome: diagnostic implications

Henrique Serigatto,Nancy Kokitsu-Nakata,Siulan Vendramini-Pittoli, Priscila Moura,Cristiano Tonello, Adriano Peixoto,Roseli Zechi-Ceide

EUROPEAN JOURNAL OF HUMAN GENETICS (2023): 220-220

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Orthodontic Treatment of Mandibular Incisor Agenesis with Herbst Appliance in a Patient with Hanhart Syndrome: A 12-Year Follow-Up

Tiago Turri de Castro Ribeiro, Helena Doneux Van der Laan,Camila Massaro,Rita de Cassia Moura Carvalho Lauris,Nancy Mizue Kokitsu-Nakata,Adriano Porto Peixoto

American journal of orthodontics and dentofacial orthopedics（2022）

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MID1 gene variations in a Brazilian cohort with cleft lip with or without palate and ocular hypertelorism. Implication for diagnosis

Roseli M. Zechi-Ceide,Nancy M. Kokitsu-Nakata,Camila Wenceslau Alvarez,Chiara Migliore,Marina Bigeli Rafacho, Maria Eugenia Siemann,Rosana M. Candido-Souza,Siulan Vendramini-Pittoli,Cristiano Tonello,Luciana P. Maximino,Germana Meroni,Maria Leine Guion-Almeida,John M. Opitz,Antonio Antonio Richieri-Costa

EUROPEAN JOURNAL OF HUMAN GENETICS（2022）

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