Skip to main content
Fig. 1 | BMC Medical Genomics

Fig. 1

From: Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literature

Fig. 1

The pedigrees, and chromatogram of studied patients. I: Family I, A: pedigree of the family, B: Sanger sequencing data of the normal, mutant hemizygous, and heterozygous female carrier of the family; II: Family II, A: pedigree of the family, B: Sanger sequencing data of the normal, mutant hemizygous and the heterozygous female carrier of the family; III: Family III, A: pedigree of the family, B: Sanger sequencing data of the normal, mutant hemizygous and the heterozygous female carrier of the family; IV: Family IV, A: pedigree of the family, B: Sanger sequencing data of the normal, mutant hemizygous and the heterozygous female carrier of the family

Back to article page

BMC Medical Genomics

ISSN: 1755-8794

Contact us