Arif O. Khan

Homozygous truncation of SIX6 causes complex microphthalmia in humans

F. Alkuraya, M. Aldahmesh, H. Hijazi, 2013, Clinical genetics.

Genetic investigation of 93 families with microphthalmia or posterior microphthalmos

A. Mansour, F. Alkuraya, M. Dasouki, 2018, Clinical genetics.

WDR19: An ancient, retrograde, intraflagellar ciliary protein is mutated in autosomal recessive retinitis pigmentosa and in Senior‐Loken syndrome

J. Majewski, F. Hildebrandt, E. Otto, 2013, Clinical genetics.