High myopia, hypertelorism, iris coloboma, exomphalos, absent corpus callosum, and sensorineural deafness: Report of a case and further evidence for autosomal recessive inheritance


Avunduk A., Aslan Y., Kapicioglu Z., Elmas R.

ACTA OPHTHALMOLOGICA SCANDINAVICA, vol.78, no.2, pp.221-222, 2000 (SCI-Expanded) identifier identifier identifier