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Cranial synostosis and Chiari 1 malformation in x-linked hypophosphatemic rickets
Mapping Intimacies
◽
10.26226/morressier.59130382d462b80292385ceb
◽
2017
◽
Author(s):
Anya Rothenbuhler
Keyword(s):
Hypophosphatemic Rickets
◽
Chiari 1 Malformation
Download Full-text
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◽
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◽
10.1016/s0276-1092(08)70038-5
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Late onset autosomal dominant hypophosphatemic rickets; confirmation of the diagnosis with genomic analysis
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Interaction between FGF23 R176W mutation and C716T nonsynonymous change (T239M, rs7955866) in FGF23 on the clinical phenotype in a family with autosomal dominant hypophosphatemic rickets
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◽
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Papilledema in a toddler: An atypical presentation of X-linked hypophosphatemic rickets
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◽
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