Ö. YAVAŞCAN, "A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings," TURKISH JOURNAL OF PEDIATRICS , vol.60, no.1, 2018
YAVAŞCAN, Ö. 2018. A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings. TURKISH JOURNAL OF PEDIATRICS , vol.60, no.1 .
YAVAŞCAN, Ö., (2018). A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings. TURKISH JOURNAL OF PEDIATRICS , vol.60, no.1.
YAVAŞCAN, Önder. "A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings," TURKISH JOURNAL OF PEDIATRICS , vol.60, no.1, 2018
YAVAŞCAN, Önder. "A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings." TURKISH JOURNAL OF PEDIATRICS , vol.60, no.1, 2018
YAVAŞCAN, Ö. (2018) . "A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings." TURKISH JOURNAL OF PEDIATRICS , vol.60, no.1.
@article{article, author={Önder YAVAŞCAN}, title={A novel homozygous W99G mutation in CLDN-16 gene causing familial hypomagnesemic hypercalciuric nephrocalcinosis in Turkish siblings}, journal={TURKISH JOURNAL OF PEDIATRICS}, year=2018}