Your browser doesn't support javascript.
loading
Association between single nucleotide polymorphism in Wnt3 and nonsyndromic cleft lip with or without cleft palate in Hui and Han population of Ningxia Autonomous Region / 华西口腔医学杂志
West China Journal of Stomatology ; (6): 397-402, 2013.
Artigo em Chinês | WPRIM | ID: wpr-336310
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the association between rs142167, rs7216231 single nucleotide polymorphism (SNP) in Wnt3 and nonsyndromic cleft lip and palate (NSCL/P) in Hui and Han population of Ningxia Autonomous Region.</p><p><b>METHODS</b>The study consisted of 371 NSCL/P patients from Ningxia Hui and Han population (Han population 166, Hui population 205), their parents (196 fathers, 224 mothers, 150 trios) and 258 normal controls (Han population 190, Hui population 68). Polymerase chain reaction-restriction fragment length polymorphisms (PCR-RFLP) was used to identify rs142167, rs7216231 genotypes of the samples. The data was analyzed by case-control analysis, transmission disequilibrium test (TDT) and family based associated test (FBAT).</p><p><b>RESULTS</b>Case-control study showed that no differences in cleft lip, cleft palate, cleft lip and palate, and the total case group compared with the control group at rs142167 and rs7216231 (P > 0.05) in Hui and Han population and in stratified comparison. TDT test showed that rs142167 and rs7216231's allele had not over-transmitted (P > 0.05) in NSCL/P. FBAT test showed that G-G specific haplotypes showed statistically significant (P < 0.05).</p><p><b>CONCLUSION</b>Wnt3 gene polymorphism is not relevant with NSCL/ P in Ningxia Hui and Han population.</p>
Assuntos
Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Polimorfismo Genético / Anormalidades Congênitas / Encéfalo / Estudos de Casos e Controles / Fenda Labial / Fissura Palatina / Polimorfismo de Nucleotídeo Único / Genótipo Tipo de estudo: Estudo observacional / Fatores de risco Limite: Humanos Idioma: Chinês Revista: West China Journal of Stomatology Ano de publicação: 2013 Tipo de documento: Artigo

Similares

MEDLINE

...
LILACS

LIS

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Assunto principal: Polimorfismo Genético / Anormalidades Congênitas / Encéfalo / Estudos de Casos e Controles / Fenda Labial / Fissura Palatina / Polimorfismo de Nucleotídeo Único / Genótipo Tipo de estudo: Estudo observacional / Fatores de risco Limite: Humanos Idioma: Chinês Revista: West China Journal of Stomatology Ano de publicação: 2013 Tipo de documento: Artigo