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1
A generalized skeletal hyperostosis in two siblings caused by a novel mutation in the SOST gene
A generalized skeletal hyperostosis in two siblings caused by a novel mutation in the SOST gene
Balemans, W., | Elsevier Inc | 2005 ,
2
An intermediate form of juvenile Paget's disease caused by a truncating TNFRSF11B mutation
An intermediate form of juvenile Paget's disease caused by a truncating TNFRSF11B mutation
Janssens, K., | Elsevier Inc | 2005 ,
3
Identification of the first deletion in the LRP5 gene in a patient with Autosomal Dominant Osteopetrosis type I
Identification of the first deletion in the LRP5 gene in a patient with Autosomal Dominant Osteopetrosis type I
Pangrazio, A., | Elsevier Inc | 2011 ,
4
Genetic analysis and effect of triiodothyronine and prednisone trial on bone turnover in a patient with craniotubular hyperostosis
Genetic analysis and effect of triiodothyronine and prednisone trial on bone turnover in a patient with craniotubular hyperostosis
López, J. M., | Elsevier Inc | 2008 ,
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