Dentinogenesis imperfecta-associated syndromes

American Journal of Medical Genetics

Volumn 104, Issue 1, 2001, Pages 75-78

  Kantaputra, Piranit N ^a  

^a CHIANG MAI UNIVERSITY   (Thailand)

Author keywords

[No Author keywords available]

Indexed keywords

AUTOSOMAL DOMINANT DISORDER; BONE DYSPLASIA; GENE EXPRESSION; GENE MUTATION; HUMAN; LETTER; OSTEOGENESIS IMPERFECTA; PRIORITY JOURNAL; SCHIMKE IMMUNOOSSEOUS DYSPLASIA; TOOTH MALFORMATION;

AGING; BONE DISEASES, DEVELOPMENTAL; DENTINOGENESIS IMPERFECTA; DENTITION, PERMANENT; HUMANS; INFANT; MALE; SYNDROME; TOOTH, DECIDUOUS;

EID: 0035889330     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10031     Document Type: Letter

References (34)

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2. Familial dentinogenesis imperfecta, blue sclerae, and wormian bones without fractures: Another type of osteogenesis imperfecta?
3. Type II collagen defect in two sibs with Goldblatt syndrome, a chondrodysplasia with dentinogenesis imperfecta, and joint laxity
4. COL5A1 exon 14 splice acceptor mutation causes a functional null allele, haploinsufficiency of alpha 1(V) and abnormal heterotypic interstitial fibrils in Ehlers-Danlos syndrome II
5. Osteogenesis imperfecta
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11. A newly recognized skeletal dysplasia with opalescent and rootless teeth
12. A Polish variant of isolated dentinogenesis imperfecta with generalized connective tissue defect
13. The dentition in osteogenesis imperfecta syndromes
14. Scanning electron microscopy of teeth in dominant osteogenesis imperfecta
15. Discrimination of morphological findings in dentin from oseogenesis imperfecta patients using combinations of polarized light microscopy, microradiiography, and scanning electron microscopy
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22. Evaluation of oral problems in an osteogenesis imperfecta population
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24. Heterogeneity of osteogenesis imperfecta type I
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27. Reduced expression of dentin sialophosphoprotein is associated with dysplastic dentin in mice overexpressing transforming growth factor-beta 1 in teeth
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31. Hereditary defects in enamel and dentin
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33. Dentinogenesis imperfecta 1 with or without progressive hearing loss is associated with distinct mutations in DSPP
34. DSPP mutation in dentinogenesis imperfecta Shields type II