Vona, B., Nanda, I., Neuner, C., Schröder, J., Kalscheuer, V. M., Shehata-Dieler, W., & Haaf, T. (2014). Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: Review of literature. BioMed Central.

Vona, Barbara, Indrajit Nanda, Cordula Neuner, Jörg Schröder, Vera M. Kalscheuer, Wafaa Shehata-Dieler, and Thomas Haaf. Terminal Chromosome 4q Deletion Syndrome in an Infant With Hearing Impairment and Moderate Syndromic Features: Review of Literature. BioMed Central, 2014.

Vona, Barbara, et al. Terminal Chromosome 4q Deletion Syndrome in an Infant With Hearing Impairment and Moderate Syndromic Features: Review of Literature. BioMed Central, 2014.