Ozturk, M. N. Et Al. 2016. Kallmann Syndrome Due to a Homozygous Missense c.217C > T (p.R73C) Mutation Detected in the Exon-2 of the PROK2 Gene. HORMONE RESEARCH IN PAEDIATRICS , vol.86 , 431-432.

Ozturk, M. N., Demirbilek, H., KOTAN, L. D., Baysal, B., Ocal, M., & TOPALOĞLU, A. K., (2016). Kallmann Syndrome Due to a Homozygous Missense c.217C > T (p.R73C) Mutation Detected in the Exon-2 of the PROK2 Gene. HORMONE RESEARCH IN PAEDIATRICS , vol.86, 431-432.

Ozturk, Mehmet Et Al. "Kallmann Syndrome Due to a Homozygous Missense c.217C > T (p.R73C) Mutation Detected in the Exon-2 of the PROK2 Gene," HORMONE RESEARCH IN PAEDIATRICS , vol.86, 431-432, 2016

Ozturk, Mehmet N. Et Al. "Kallmann Syndrome Due to a Homozygous Missense c.217C > T (p.R73C) Mutation Detected in the Exon-2 of the PROK2 Gene." HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.431-432, 2016

Ozturk, M. N. Et Al. (2016) . "Kallmann Syndrome Due to a Homozygous Missense c.217C > T (p.R73C) Mutation Detected in the Exon-2 of the PROK2 Gene." HORMONE RESEARCH IN PAEDIATRICS , vol.86, pp.431-432.

@article{article, author={Mehmet Nuri Ozturk Et Al. }, title={Kallmann Syndrome Due to a Homozygous Missense c.217C > T (p.R73C) Mutation Detected in the Exon-2 of the PROK2 Gene}, journal={HORMONE RESEARCH IN PAEDIATRICS}, year=2016, pages={431-432} }