Triple X syndrome plus translocation between Xp and 6p associated with x-linked hypophosphatemic rickets: identification of breakpoint within the PHEX -gene

Bibliographic Details
Main Authors:	Riedl, S. (Author), Schober, E. (Author), Frisch, H. (Author)
Format:	Article
Language:	Slovak English
Subjects:	syndróm XXX hypofosfatémia trizómia rachitída články z novín a časopisov

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