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van buchem disease
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Genetic Markers
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SOST
LRP5
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Pathway Enrichment
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Sclerostin
Sclerostin/Sclerostin domain-containing protein 1
regulation of ossification
GSE6259_BCELL_VS_CD4_TCELL_UP
HEN1_02
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OMIM - van Buchem disease
OMIM - Congenital disorder
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Van Buchem disease: First case report in Taiwan.
Genetics of Sost/SOST in Sclerosteosis and van Buchem Disease Animal Models.
Decompressive surgery in a patient with hyperostosis corticalis generalisata for relief of cognitive…
A rare cause of facial nerve palsy in children: hyperostosis corticalis generalisata (Van Buchem dis…
Van Buchem disease: clinical, biochemical, and densitometric features of patients and disease carrie…
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ECAA Brain MRI: Seeking the Link Between Extracranial Carotid Artery Aneurysms and Small Vessel Dise…
The Role Of FGF23, Klotho, And Sclerostin In Kidney Stone Formers
Bone Response to Exercise in Women on Antiresorptive Medications
Neuroimaging Combining Biomarkers for Identifying Long-term Cognitive Dysfunction and Delirium
Comparison of Anti-coagulation and Anti-Platelet Therapies for Intracranial Vascular Atherostenosis-…
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