Hyperplastic callus and osteogenesis imperfecta

Lancet

Volumn 357, Issue 9252, 2001, Pages 248-249

  Smith, Roger ^a  

^a NUFFIELD ORTHOPAEDIC CENTRE   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

COLLAGEN TYPE 1;

AUTOSOMAL DOMINANT DISORDER; CALLUS; DISEASE CLASSIFICATION; GENE MUTATION; HUMAN; HYPERPLASTIC CALLUS; NOTE; OSTEOGENESIS IMPERFECTA; PRIORITY JOURNAL; SYNDROME;

EID: 0035956664     PISSN: 01406736     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0140-6736(00)03607-2     Document Type: Note

References (9)

1. The brittle bone syndrome: An update
2. Familial occurrence of hyperplastic callus in osteogenesis imperfecta
3. Type V osteogenesis imperfecta: A new form of brittle bone disease
4. Osteoporosis-pseudoglioma syndrome, a disorder affecting skeletal strength and vision, is assigned to chromosome region 11q12-13
5. Osteogenesis imperfecta with arthrogryposis multiplex congenita (Bruck syndrome): Evidence for possible autosomal recessive inheritance
6. Osteogenesis imperfecta
7. MRI and CT features of hyperplastic callus in osteogenesis imperfecta tarda
8. Progressive osseous heteroplasia
9. Stem cells near the century mark