Fig. 2From: Clinical profile of comorbidity of rare diseases in a Tunisian patient: a case report associating incontinentia pigmenti and Noonan syndromeSequencing results. a IGV browser visualization of the targeted NGS sequencing results showing the heterozygous c.788 T > G substitution in the RAF1 gene in the patient, (reverse sequence) which is absent in another NS patient (used as a control); b Sanger sequencing confirming the de novo appearance of the mutation in the patient, given its absence in the parents’ DNA samplesBack to article page