m. n. özbek Et Al. , "Kallmann Syndrome Due to a Homozygous Missense c.217CT (p.R73C) Mutation Detected in the Exon-2 of the PROK2 Gene," European Society for Paediatric Endocrinology 2016 , 2016
özbek, m. n. Et Al. 2016. Kallmann Syndrome Due to a Homozygous Missense c.217CT (p.R73C) Mutation Detected in the Exon-2 of the PROK2 Gene. European Society for Paediatric Endocrinology 2016 .
özbek, m. n., DEMİRBİLEK, H., KOTAN GEDİK, L. D., BAYSAL, B., ocal, m., & TOPALOĞLU, A. K., (2016). Kallmann Syndrome Due to a Homozygous Missense c.217CT (p.R73C) Mutation Detected in the Exon-2 of the PROK2 Gene . European Society for Paediatric Endocrinology 2016
özbek, mehmet Et Al. "Kallmann Syndrome Due to a Homozygous Missense c.217CT (p.R73C) Mutation Detected in the Exon-2 of the PROK2 Gene," European Society for Paediatric Endocrinology 2016, 2016
özbek, mehmet n. Et Al. "Kallmann Syndrome Due to a Homozygous Missense c.217CT (p.R73C) Mutation Detected in the Exon-2 of the PROK2 Gene." European Society for Paediatric Endocrinology 2016 , 2016
özbek, m. n. Et Al. (2016) . "Kallmann Syndrome Due to a Homozygous Missense c.217CT (p.R73C) Mutation Detected in the Exon-2 of the PROK2 Gene." European Society for Paediatric Endocrinology 2016 .
@conferencepaper{conferencepaper, author={mehmet nuri özbek Et Al. }, title={Kallmann Syndrome Due to a Homozygous Missense c.217CT (p.R73C) Mutation Detected in the Exon-2 of the PROK2 Gene}, congress name={European Society for Paediatric Endocrinology 2016}, city={}, country={}, year={2016}}