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Association between the JAG2 gene polymorphism and the occurrence of nonsyndromic cleft lip with or without cleft palate in northwest Chinese population / 中华医学遗传学杂志
Chinese Journal of Medical Genetics ; (6): 75-79, 2020.
Artigo em Chinês | WPRIM | ID: wpr-781289
ABSTRACT
OBJECTIVE@#To assess the association of JAG2 gene single nucleotide polymorphisms with the occurrence of nonsyndromic cleft lip with or without cleft palate (NSCLP) among northwest Chinese population.@*METHODS@#A case-control study was carried out on 301 NSCLP patients and 304 healthy controls. An iMLDR(TM) genotyping technique was used to detect three single nucleotide polymorphisms (SNPs) [rs741859 (T/C), rs11621316 (A/G) and rs1057744(C/T)] of the JAG2 gene. Allelic and genotypic frequencies and haplotypic distribution among the two groups were compared.@*RESULTS@#A significant difference was found in the frequency of C and T alleles for rs741859 between the two groups. The CT genotype of rs741859 could significantly reduce the risk for NSCLP to 65% (P 0.8), whose distribution difference between the two groups was not statistically significant (P> 0.05).@*CONCLUSION@#The CT genotype of the JAG2 gene rs741859 may confer a protective effect for NSCLP among northwest Chinese population.
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Estudos de Casos e Controles / China / Fenda Labial / Fissura Palatina / Polimorfismo de Nucleotídeo Único / Proteína Jagged-2 / Frequência do Gene / Genética / Genótipo Tipo de estudo: Estudo observacional / Fatores de risco Limite: Humanos País/Região como assunto: Ásia Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2020 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Estudos de Casos e Controles / China / Fenda Labial / Fissura Palatina / Polimorfismo de Nucleotídeo Único / Proteína Jagged-2 / Frequência do Gene / Genética / Genótipo Tipo de estudo: Estudo observacional / Fatores de risco Limite: Humanos País/Região como assunto: Ásia Idioma: Chinês Revista: Chinese Journal of Medical Genetics Ano de publicação: 2020 Tipo de documento: Artigo