T. GÜRAN Et Al. , "PPP2R3C gene variants cause syndromic 46,XY gonadal dysgenesis and impaired spermatogenesis in humans," European Journal of Endocrinology , vol.180, no.5, pp.291-309, 2019
GÜRAN, T. Et Al. 2019. PPP2R3C gene variants cause syndromic 46,XY gonadal dysgenesis and impaired spermatogenesis in humans. European Journal of Endocrinology , vol.180, no.5 , 291-309.
GÜRAN, T., YEŞİL SAYIN, G., DEMİRCİOĞLU, S., ATAY, Z., BOZKURTLAR, E., Aghayev, A., ... Gul, S.(2019). PPP2R3C gene variants cause syndromic 46,XY gonadal dysgenesis and impaired spermatogenesis in humans. European Journal of Endocrinology , vol.180, no.5, 291-309.
GÜRAN, TÜLAY Et Al. "PPP2R3C gene variants cause syndromic 46,XY gonadal dysgenesis and impaired spermatogenesis in humans," European Journal of Endocrinology , vol.180, no.5, 291-309, 2019
GÜRAN, TÜLAY Et Al. "PPP2R3C gene variants cause syndromic 46,XY gonadal dysgenesis and impaired spermatogenesis in humans." European Journal of Endocrinology , vol.180, no.5, pp.291-309, 2019
GÜRAN, T. Et Al. (2019) . "PPP2R3C gene variants cause syndromic 46,XY gonadal dysgenesis and impaired spermatogenesis in humans." European Journal of Endocrinology , vol.180, no.5, pp.291-309.
@article{article, author={TÜLAY GÜRAN Et Al. }, title={PPP2R3C gene variants cause syndromic 46,XY gonadal dysgenesis and impaired spermatogenesis in humans}, journal={European Journal of Endocrinology}, year=2019, pages={291-309} }