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Investigating deafness genes as a cause of sudden sensorineural hearing loss
(Sociedade Brasileira de Genática - SBGÁguas de Lindóia, 2013-09-16)
Hearing loss is a very heterogeneous genetic condition, meaning that identical or similar phenotypes result from
mutations in many di erent genes, with diverse inheritance mechanisms. Sudden sensorineural hearing loss ...
The importance of genetic studies in children with hearing loss ascertained after universal neonatal hearing screening (UNHS)
(Sociedade Brasileira de Genática - SBGÁguas de Lindóia, 2013-09)
Universal Neonatal Hearing Screening (UNHS) is mandatory in the state of São Paulo and it has been performed as a
routine in all public hospitals from “Rede de Proteção Mãe Paulistana” in the city of São Paulo, since ...
Phenotypic refinement of the mandibulofacial dysostosis Bauru type
(Universidade de São Paulo, Hospital de Reabilitação de Anomalias CraniofaciaisBauru, 2013-11-08)
Purpose: Refine the MFD Bauru type syndrome phenotype; Investigate the mandible, maxilla, zigomatic arch on the sample, using radiological evaluation. Methods: 11 subjects were included on this study with clinical diagnosis ...