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.
Chicago-стиль цитированияHampson, Geeta, Martin A. Konrad, and John Scoble. Familial Hypomagnesaemia With Hypercalciuria and Nephrocalcinosis (FHHNC): Compound Heterozygous Mutation in the Claudin 16 (CLDN16) Gene. BioMed Central, 2008.
MLA-цитированиеHampson, Geeta, Martin A. Konrad, and John Scoble. Familial Hypomagnesaemia With Hypercalciuria and Nephrocalcinosis (FHHNC): Compound Heterozygous Mutation in the Claudin 16 (CLDN16) Gene. BioMed Central, 2008.
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