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American Journal of Medical Genetics. Part A|March 31, 2016
Apert and Crouzon syndromes-Cognitive development, brain abnormalities, and molecular aspectsMarilyse B L Fernandes, Luciana P Maximino, Gimol B Perosa, et al.American Journal of Medical Genetics. Part A|November 26, 2010
Identification of a microdeletion at the 7q33-q35 disrupting the CNTNAP2 gene in a Brazilian stuttering caseAline L Petrin, Célia M Giacheti, Luciana P Maximino, et al.American Journal of Medical Genetics. Part A|January 29, 2011
Richieri-Costa-Pereira syndrome: a unique acrofacial dysostosis type. An overview of the Brazilian casesFrancine Pinheiro Favaro, Roseli Maria Zechi-Ceide, Camila Wenceslau Alvarez, et al.The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|February 27, 2010
Saethre-Chotzen syndrome, Pro136His TWIST mutation, hearing loss, and external and middle ear structural anomalies: report on a Brazilian familyDionísia A C Lamônica, Luciana P Maximino, Mariza Ribeiro Feniman, et al.American Journal of Medical Genetics. Part A|April 28, 2009
Possible new syndrome: Left ventricular noncompaction, partial agenesis of the corpus callosum, and developmental delay in a Brazilian childDionisia A C Lamonica, Dagma V M Abramides, Luciana P Maximino, et al.Pageof 1