Links
[1] http://ghr.nlm.nih.gov/gene/CHD7
[2] http://ghr.nlm.nih.gov/gene/SEMA3E
[3] https://disorders.eyes.arizona.edu/references/mutation-update-chd7-gene-involved-charge-syndrome
[4] https://disorders.eyes.arizona.edu/references/chd7-mutations-patients-initially-diagnosed-kallmann-syndrome-clinical-overlap-charge
[5] https://disorders.eyes.arizona.edu/references/familial-charge-syndrome-and-chd7-gene-recurrent-missense-mutation-intrafamilial
[6] https://disorders.eyes.arizona.edu/references/spectrum-chd7-mutations-110-individuals-charge-syndrome-and-genotype-phenotype
[7] https://disorders.eyes.arizona.edu/references/updated-diagnostic-criteria-charge-syndrome-proposal