Links
[1] http://ghr.nlm.nih.gov/gene/ESCO2
[2] http://omim.org/entry/269000
[3] https://disorders.eyes.arizona.edu/disorders/baller-gerold-syndrome
[4] http://omim.org/entry/218600
[5] http://ghr.nlm.nih.gov/gene/RECQL4
[6] https://disorders.eyes.arizona.edu/references/roberts-syndrome-deficit-acetylated-cohesin-leads-nucleolar-dysfunction
[7] https://disorders.eyes.arizona.edu/references/roberts-syndromesc-phocomelia-spectrum-case-report-adult-review-literature
[8] https://disorders.eyes.arizona.edu/references/cytogenetic-findings-roberts-sc-phocomelia-syndromes
[9] https://disorders.eyes.arizona.edu/references/sc-phocomelia-and-roberts-syndrome-nosologic-aspects