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Focal growth disturbances
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- Journal Article
- A1
- open access
Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly : high incidence of epilepsy
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- Journal Article
- A1
- open access
Consensus recommendations for the diagnosis and management of X-linked hypophosphatemia in Belgium
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Caffey disease is associated with distinct arginine to cysteine substitutions in the proα1(I) chain of type I procollagen
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- Journal Article
- A1
- open access
Destructive juvenile idiopathic arthritis : do not overlook rare genetic skeletal disorders
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- Journal Article
- A1
- open access
Fibrous dysplasia, Paget's disease of bone, and other uncommon sclerotic bone lesions of the craniofacial bones
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- Journal Article
- A2
- open access
Een patiënt met dense botten
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Une patiente avec des os denses
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Camurati-Engelmann disease
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- Journal Article
- A1
- open access
Diagnosing enterovirus meningitis via blood transcriptomics : an alternative for lumbar puncture?