Riedl, S., Schober, E., & Frisch, H. Triple X syndrome plus translocation between Xp and 6p associated with x-linked hypophosphatemic rickets: Identification of breakpoint within the PHEX -gene.
Citácia podľa Chicago (17th ed.)Riedl, S., E. Schober, a H. Frisch. Triple X Syndrome Plus Translocation Between Xp and 6p Associated with X-linked Hypophosphatemic Rickets: Identification of Breakpoint Within the PHEX -gene.
Citácia podľa MLA (8th ed.)Riedl, S., et al. Triple X Syndrome Plus Translocation Between Xp and 6p Associated with X-linked Hypophosphatemic Rickets: Identification of Breakpoint Within the PHEX -gene.
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