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American Journal of Medical Genetics. Part A|July 11, 2013
A compound heterozygote SLC26A2 mutation resulting in robin sequence, mild limbs shortness, accelerated carpal ossification, and multiple epiphysial dysplasia in two Brazilian sisters. A new intermediate phenotype between diastrophic dysplasia and recessive multiple epiphyseal dysplasiaRoseli Maria Zechi-Ceide, Priscila Padilha Moura, Salmo Raskin, et al.American Journal of Orthodontics and Dentofacial Orthopedics : Official Publication of the American Association of Orthodontists, Its Constituent Societies, and the American Board of Orthodontics|October 18, 2021
Three-dimensional comparison of mandibular morphology in young people with Treacher Collins syndrome and Pierre Robin sequenceRenata Mayumi Kato, Priscila Padilha Moura, Roseli Maria Zechi-Ceide, et al.The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|July 3, 2020
Comparison Between Treacher Collins Syndrome and Pierre Robin Sequence: A Cephalometric StudyRenata Mayumi Kato, Priscila Padilha Moura, Roseli Maria Zechi-Ceide, et al.American Journal of Medical Genetics. Part A|June 7, 2023
Oculoauriculofrontonasal syndrome: Refining the phenotype through a new case series and literature reviewHenrique Regonaschi Serigatto, Nancy Mizue Kokitsu-Nakata, Siulan Vendramini-Pittoli, et al.The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|March 30, 2026
Unusual Association of Orofacial Cleft and Finger-Like Skin Appendages With or Without Constriction Rings: A Disorganization-Like Phenotype?Henrique Regonaschi Serigatto, Siulan Vendramini-Pittoli, Priscila Padilha Moura, et al.American Journal of Human Genetics|March 17, 2015
Mutations in the endothelin receptor type A cause mandibulofacial dysostosis with alopeciaChristopher T Gordon, K Nicole Weaver, Roseli Maria Zechi-Ceide, et al.Pageof 1