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Abstract This study was performed to: Explore the presence of MSX1 gene mutation in a sample of Egyptian patients suffering from nonsyndromic cleft lip with or without cleft palate using sequence analysis. Correlate between the genomic data in relation to type of cleft and missing teeth if present. Explore an early genetic diagnostic aid in premarital examination for individuals with familial history of non-syndromic cleft lip with or without cleft palate. |