Showing results (11-20 of 33) with videos related to
Sort By:
Pageof 4
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 29, 2010
Mandibulofacial dysostosis, severe lower eyelid coloboma, cleft palate, and alopecia: A new distinct form of mandibulofacial dysostosis or a severe form of Johnson-McMillin syndrome?Roseli Maria Zechi-Ceide, Maria Leine Guion-Almeida, Fernanda Sarquis Jehee, et al.American Journal of Medical Genetics. Part A|May 26, 2012
Frontonasal dysplasia, callosal agenesis, basal encephalocele, and eye anomalies syndrome with a partial 21q22.3 deletionMaria Leine Guion-Almeida, Antonio Richieri-Costa, Fernanda Sarquis Jehee, et al.American Journal of Medical Genetics. Part A|May 29, 2024
Hemiarhinia caused by a missense variation in SMCHD1: A mild phenotype in the clinical spectrum of Bosma arhinia microphthalmia syndromeNancy Mizue Kokitsu-Nakata, Vinicius Contrucci Dantas Segarra, Cristiano Tonello, et al.American Journal of Medical Genetics. Part A|May 19, 2009
Holoprosencephaly, ectrodactyly, and bilateral cleft of lip and palate: exclusion of SHH, TGIF, SIX3, GLI2, TP73L, and DHCR7 as candidate genesRoseli Maria Zechi-Ceide, Lucilene Arilho Ribeiro, Salmo Raskin, et al.The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|September 1, 2025
Cognitive and Behavioral Characteristics of Children with Robin Sequence Associated with Stickler Syndrome: A Case SeriesJuliana Garcia Martins, Pâmella de Oliveira Ladeia, Roseli Maria Zechi-Ceide, et al.Clinical Dysmorphology|June 7, 2007
Hydrocephalus and moderate mental retardation in a boy with Van der Woude phenotype and IRF6 gene mutationRoseli Maria Zechi-Ceide, Maria Leine Guion-Almeida, Elaine Sbroggio de Oliveira Rodini, et al.Journal of Pediatric Genetics|May 13, 2017
Multisystem Involvement in a Patient with a PTCH1 Mutation: Clinical and Imaging FindingsAntonio Richieri-Costa, Siulan Vendramini-Pittoli, Nancy Mizue Kokitsu-Nakata, et al.American Journal of Medical Genetics. Part A|May 26, 2012
Saethre-Chotzen phenotype with learning disability and hyper IgE phenotype in a patient due to complex chromosomal rearrangement involving chromosomes 3 and 7Roseli Maria Zechi-Ceide, Melina Guerreiro Rodrigues, Fernanda Sarquis Jehee, et al.American Journal of Medical Genetics. Part A|November 23, 2011
Auriculo-condylar syndrome. Confronting a diagnostic challengeNancy Mizue Kokitsu-Nakata, Roseli Maria Zechi-Ceide, Siulan Vendramini-Pittoli, et al.Pageof 4