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This method was used not only to quantify the copy numbers of highly homogenous telomeric <jats:italic>SMN<\/jats:italic> (<jats:italic>SMN1<\/jats:italic>)<jats:italic>\/<\/jats:italic>centromeric <jats:italic>SMN<\/jats:italic> genes in exons 7 and 8 but also to determine intragenic mutations in all nine exons for complete diagnosis of spinal muscular atrophy (SMA). Additionally, we utilized the \u201cuniversal fluorescent PCR\u201d for simultaneously fluorescent labeling of eleven gene fragments (nine exons in SMN and two internal standards). Such technique is very beneficial for multi\u2010exon analysis due to only requirement of one universal fluorescent primer which could fluorescently amplify all gene fragments. Of all 262 detected individuals, three subjects possessing different ratios of <jats:italic>SMN1\/<\/jats:italic>centromeric <jats:italic>SMN<\/jats:italic> in the two exons were determined as gene conversion, and we also detected three interesting intragenic mutations (c.1 \u201039A&gt;G, c.22_23insA in exon 1, c.84C&gt;T in exon 2a) which were associated with the SMA patients owning one copy of <jats:italic>SMN1<\/jats:italic> including two mutations never reported previously. This high\u2010resolved method provided better potential technique for genotyping and identifying SMA, carrier and normal controls in large population.<\/jats:p>","DOI":"10.1002\/elps.201000124","type":"journal-article","created":{"date-parts":[[2010,7,12]],"date-time":"2010-07-12T11:26:10Z","timestamp":1278933970000},"page":"2396-2404","source":"Crossref","is-referenced-by-count":16,"title":["Multi\u2010exon genotyping of <i>SMN<\/i> gene in spinal muscular atrophy by universal fluorescent PCR and capillary 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