For citations:
Buianova A.A., Rozhkova A.V., Parshina O.P., Kudakaeva A.A., Vasilyev E.V., Dantsev I.S., Nikolaeva E.A. Experience of using whole genome sequencing for diagnostics of X-linked hypophosphatemic rickets on the example of two cases. Rossiyskiy Vestnik Perinatologii i Pediatrii (Russian Bulletin of Perinatology and Pediatrics). 2025;70(6):95-103. (In Russ.) https://doi.org/10.21508/1027-4065-2025-70-6-95-103
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