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Rev. méd. Chile ; 126(6): 637-45, jun. 1998. ilus, tab
Artigo em Espanhol | LILACS | ID: lil-229005

RESUMO

Background: Homeotic genes have regulatory functions during development. It has been postulated that the human Msx-1 homeotic gene can be involved in the etiology of non syndromic cleft lip palate, since its homologous Msx-1 is involved in cleft palate of mice. Aim: To perform an association analysis between the genetic variation of Msx-1 and non syndromic cleft lip palate in Chilean subjects. Patients and methods: Seventy patients with non syndromic cleft lip palate, 136 healthy relatives of these patients and 69 non related normal individuals were studied. CA microsatellite in Msx- gene, that was amplified with PCR, was studied. Results: No differences in the genetic frequencies of Msx-1 alleles, were observed in the three groups studied. Allelic heterogeneity for allele 2 seems to be related to cases of non syndromic cleft lip palate from multiplex families and heterogeneity for allele 3 is related with simplex families cases. Conclusions: These results seem to support the hypothesis of genetic heterogeneity in the etiology of non syndromic cleft lip palate


Assuntos
Humanos , Masculino , Feminino , Fenda Labial/genética , Fissura Palatina/genética , Alelos , Modelos Genéticos , Frequência do Gene/genética
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