Hampson, G., Konrad, M. A., & Scoble, J. (2008). Familial hypomagnesaemia with hypercalciuria and nephrocalcinosis (FHHNC): Compound heterozygous mutation in the claudin 16 (CLDN16) gene. BioMed Central.
استشهاد بنمط شيكاغوHampson, Geeta, Martin A. Konrad, و John Scoble. Familial Hypomagnesaemia With Hypercalciuria and Nephrocalcinosis (FHHNC): Compound Heterozygous Mutation in the Claudin 16 (CLDN16) Gene. BioMed Central, 2008.
MLA استشهادHampson, Geeta, Martin A. Konrad, و John Scoble. Familial Hypomagnesaemia With Hypercalciuria and Nephrocalcinosis (FHHNC): Compound Heterozygous Mutation in the Claudin 16 (CLDN16) Gene. BioMed Central, 2008.
تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.