Skip to main content
Fig. 1 | BMC Medical Genomics

Fig. 1

From: Consider CUX1 variants in children with a variation of sex development: a case report and review of the literature

Fig. 1

A novel familial variant in CUX1 associated with VSD and neurodevelopmental differences. a picture of the proband highlighting facial features b pedigree illustrating the proband (arrow), the maternally inherited CUX1 variant (4), maternal uncle with hypospadias who has not undergone segregation testing (5), and neurodevelopmental differences on both sides (denoted by the grey shading)

Back to article page

BMC Medical Genomics

ISSN: 1755-8794

Contact us