Concepedia

Publication | Open Access

X-linked hypophosphatemic rickets: Case report

DOIFull Paper Access

14

Citations

13

References

2014

Year

Vladimir Radlović, Željko Smoljanić, Nedeljko Radlović, Zoran Leković, Dragana Ristić, Siniša Dučić, Polina Pavićević
Srpski arhiv za celokupno lekarstvo

Abstract

Identification of genetic defects is exceptionally significant for diagnosis and differential diagnosis of hereditary HR.

References

YearCitations

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