Results 181 to 190 of about 7,940 (235)

Genotype-phenotype correlations in 294 pediatric patients with osteogenesis imperfecta. [PDF]

open access: yesJBMR Plus
Byrd JJ   +6 more
europepmc   +1 more source

Orthodontic Management in Pediatric Patients with Rare Diseases: Case Reports. [PDF]

open access: yesJ Clin Med
Luzzi V   +8 more
europepmc   +1 more source

Rare dentin defects: Understanding the pathophysiological mechanisms of COLXVA1 mutations. [PDF]

open access: yesGenes Dis
Bugueno IM   +8 more
europepmc   +1 more source

Home - About - Disclaimer - Privacy