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American Journal of Medical Genetics. Part A|November 7, 2007
Cerebro-oculo-nasal syndrome: 13 new Brazilian casesMaria Leine Guion-Almeida, Roseli Maria Zechi-Ceide, Antonio Richieri-Costa
Clinical Dysmorphology|December 1, 2007
Holoprosencephaly spectrum, ano/microphthalmia, and first branchial arch defects: evidence for a new disorderMaria Leine Guion-Almeida, Antonio Richieri-Costa, Roseli Maria Zechi-Ceide
American Journal of Medical Genetics. Part A|October 2, 2007
Occipital atretic cephalocele, striking facial anomalies, and large feet in three siblings of a consanguineous unionRoseli Maria Zechi-Ceide, Maria Leine Guion-Almeida, Sthella Zanchetta, et al.
American Journal of Medical Genetics. Part A|February 14, 2024
Monodactyly in a patient with CHARGE syndrome: An additional case reportHenrique Regonaschi Serigatto, Roseli Maria Zechi-Ceide, Isabella Parizotto, et al.
Clinical Dysmorphology|June 9, 2006
A new syndrome with growth and mental retardation, mandibulofacial dysostosis, microcephaly, and cleft palateMaria Leine Guion-Almeida, Roseli Maria Zechi-Ceide, Siulan Vendramini, et al.
American Journal of Medical Genetics|September 24, 2002
Auriculo-condylar syndrome: additional patientsMaria Leine Guion-Almeida, Roseli Maria Zechi-Ceide, Siulan Vendramini, et al.
American Journal of Medical Genetics. Part A|June 20, 2012
Laryngeal malformation in Richieri-Costa Pereira syndrome: new findingsHaline Coracine Miguel, Christiano Giácomo Carneiro, Alfredo Tabith, et al.
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 Medical Genetics. Part A|November 19, 2009
Mandibulofacial syndrome with growth and mental retardation, microcephaly, ear anomalies with skin tags, and cleft palate in a mother and her son: autosomal dominant or X-linked syndrome?Maria Leine Guion-Almeida, Siulan Vendramini-Pittoli, Maria Rita Santos Passos-Bueno, 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.
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