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Triple X syndrome plus translocation between Xp and 6p associated with X-linked hypophosphatemic rickets: identification of breakpoint within the PHEX-gene
Title Triple X syndrome plus translocation between Xp and 6p associated with X-linked hypophosphatemic rickets: identification of breakpoint within the PHEX-gene Author info S. Riedl, E. Schober, H. Frisch Title XXX syndróm plus translokácia medzi Xp a 6p združená s X-viazanou hypofosfatemickou krivicou: identifikácia miesta zlomu v PHEX-géne Author Riedl Stefan
Co-authors Schober E.
Frisch H.
Corporation Middle European Workshop of Paediatric Endocrinologists 6., 1999, Emmersdorf, Rakúsko
Note Abstrakta zo 6.Stredoeurópskej konferencie pediatrických endokrinológov. - The 6th Middle European Workshop of Paediatric Endocrinology /MEWPE 1999/,. - Emmersdorf, Austria, November 19-21, 1999 Sign. C 1685 Source Endocrine regulations. - ISSN 1210-0668 . - ISSN 1336-0329 . - Roč. 34, č. 1 (2000), s. 49-50 systematics 616.71-008:575.224:061.3 MeSH Subject rachitída hypofosfatemická familiárna : genetika
trizómia
translokácia genetická
Subj. Headings gén PHEX Language English Country Slovak Republic Document kind Rozpis článkov z periodík Database ARTICLES 
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Number of the records: 1