Skip to main content
Fig. 3 | BMC Medical Genetics

Fig. 3

From: Premature ovarian insufficiency as a variable feature of blepharophimosis, ptosis, and epicanthus inversus syndrome associated with c.223C > T p.(Leu75Phe) FOXL2 mutation: a case report

Fig. 3

Sequencing results: a Pedigree of studied family, proband is marked with black arrow. b Next-generation Sequencing results of c.223C > T p.(Leu75Phe) variant in the FOXL2 gene in the proband using Integrative Genomic Viewer (IGV). c Amplicon deep sequencing (ADS) results in the FOXL2 gene in the studied family (IGV view)

Back to article page

BMC Medical Genetics

ISSN: 1471-2350

Contact us