Links
[1] http://ghr.nlm.nih.gov/gene/HCCS
[2] http://ghr.nlm.nih.gov/gene/COX7B
[3] https://disorders.eyes.arizona.edu/disorders/focal-dermal-hypoplasia
[4] http://www.ncbi.nlm.nih.gov/omim/305600
[5] http://disorders.eyes.arizona.edu/disorders/focal-dermal-hypoplasia
[6] http://ghr.nlm.nih.gov/gene/PORCN
[7] https://disorders.eyes.arizona.edu/disorders/incontinentia-pigmenti
[8] http://www.ncbi.nlm.nih.gov/omim/308300
[9] https://disorders.eyes.arizona.edu/disorders/aicardi-syndrome
[10] http://www.ncbi.nlm.nih.gov/omim/304050
[11] http://ghr.nlm.nih.gov/gene/IKBKG
[12] https://disorders.eyes.arizona.edu/references/mutations-cox7b-cause-microphthalmia-linear-skin-lesions-unconventional-mitochondrial
[13] https://disorders.eyes.arizona.edu/references/hccs-loss-function-missense-mutation-female-bilateral-microphthalmia-and-sclerocornea
[14] https://disorders.eyes.arizona.edu/references/mutations-mitochondrial-holocytochrome-c-type-synthase-x-linked-dominant-microphthalmia
[15] https://disorders.eyes.arizona.edu/references/microphthalmia-linear-skin-defects-syndrome-mosaic-female-infant-monosomy-xp22-region