Fig. 1From: An integration into the diagnostic workflow in a pediatric patient suspected of having Marfan syndromeDiagram of the pedigree tree for the missense c.5371 T > A mutation in the FBN1 gene. IGV software (Integrative genomics viewer) displays FBN1 genotypes for the father (T/T), mother (T/T), and proband (A/T), with validation using Sanger sequencingBack to article page