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Fig. 3 | BMC Medical Genetics

Fig. 3

From: Detection of a heterozygous germline APC mutation in a three-generation family with familial adenomatous polyposis using targeted massive parallel sequencing in Vietnam

Fig. 3

Validation of the deletion in affected members using Sanger sequencing. (Top) The heterozygous deletion c.3927_3931delAAAGA in proband II-2: the deletion causes a frameshift and creates a Stop codon downstream. (Bottom) The complete sequence in unaffected members. The blue vertical line represents the last base before deletion

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BMC Medical Genetics

ISSN: 1471-2350

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