A. Avunduk Et Al. , "High myopia, hypertelorism, iris coloboma, exomphalos, absent corpus callosum, and sensorineural deafness: Report of a case and further evidence for autosomal recessive inheritance," ACTA OPHTHALMOLOGICA SCANDINAVICA , vol.78, no.2, pp.221-222, 2000
Avunduk, A. Et Al. 2000. High myopia, hypertelorism, iris coloboma, exomphalos, absent corpus callosum, and sensorineural deafness: Report of a case and further evidence for autosomal recessive inheritance. ACTA OPHTHALMOLOGICA SCANDINAVICA , vol.78, no.2 , 221-222.
Avunduk, A., Aslan, Y., Kapicioglu, Z., & Elmas, R., (2000). High myopia, hypertelorism, iris coloboma, exomphalos, absent corpus callosum, and sensorineural deafness: Report of a case and further evidence for autosomal recessive inheritance. ACTA OPHTHALMOLOGICA SCANDINAVICA , vol.78, no.2, 221-222.
Avunduk, AM Et Al. "High myopia, hypertelorism, iris coloboma, exomphalos, absent corpus callosum, and sensorineural deafness: Report of a case and further evidence for autosomal recessive inheritance," ACTA OPHTHALMOLOGICA SCANDINAVICA , vol.78, no.2, 221-222, 2000
Avunduk, AM Et Al. "High myopia, hypertelorism, iris coloboma, exomphalos, absent corpus callosum, and sensorineural deafness: Report of a case and further evidence for autosomal recessive inheritance." ACTA OPHTHALMOLOGICA SCANDINAVICA , vol.78, no.2, pp.221-222, 2000
Avunduk, A. Et Al. (2000) . "High myopia, hypertelorism, iris coloboma, exomphalos, absent corpus callosum, and sensorineural deafness: Report of a case and further evidence for autosomal recessive inheritance." ACTA OPHTHALMOLOGICA SCANDINAVICA , vol.78, no.2, pp.221-222.
@article{article, author={AM Avunduk Et Al. }, title={High myopia, hypertelorism, iris coloboma, exomphalos, absent corpus callosum, and sensorineural deafness: Report of a case and further evidence for autosomal recessive inheritance}, journal={ACTA OPHTHALMOLOGICA SCANDINAVICA}, year=2000, pages={221-222} }