Oropharyngeal skeletal disease accompanying high bone mass and novel LRP5 mutation. [electronic resource]
Producer: 20050819Description: 878-85 p. digitalISSN:- 0884-0431
- Alleles
- Base Sequence
- Bone Density -- genetics
- Bone Diseases -- genetics
- Bone and Bones -- pathology
- Exons
- Female
- Heterozygote
- Humans
- Intercellular Signaling Peptides and Proteins -- metabolism
- LDL-Receptor Related Proteins -- genetics
- Low Density Lipoprotein Receptor-Related Protein-5
- Male
- Mandible -- diagnostic imaging
- Middle Aged
- Models, Genetic
- Molecular Sequence Data
- Mutation
- Mutation, Missense
- Osteogenesis -- physiology
- Palate -- pathology
- Pedigree
- Phenotype
- Radiography
- Signal Transduction
- Skull -- diagnostic imaging
- Syndrome
- Wnt Proteins
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
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