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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 : The 6th Middle European Workshop on Paediatric Endocrinology (MEWPE 1999), Emmersdorf, Austria, November 19-21, 1999. Abstrakt
S. Riedl, E. Schober, H. Frisch
Endocrine regulations.
2000 ;
Roč. 34 (č. 1) :
s. 49-50.
Language English Country Slovakia
Document type Case Reports
Persistent link
https://www.medvik.cz/link/bmc00008759
Online
NLK
ROAD: Directory of Open Access Scholarly Resources
from 1998
- MeSH
- X Chromosome pathology MeSH
- Chromosome Aberrations diagnosis complications therapy MeSH
- Child MeSH
- Hypophosphatemia drug therapy genetics complications MeSH
- Infant MeSH
- Drug Therapy, Combination MeSH
- Humans MeSH
- Infant, Newborn MeSH
- Rickets drug therapy genetics complications MeSH
- Check Tag
- Child MeSH
- Infant MeSH
- Humans MeSH
- Infant, Newborn MeSH
- Female MeSH
- Publication type
- Case Reports MeSH
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