Research Topics
| M J AldredSummaryCountry: Australia Publications
| Collaborators
|
Detail Information
Publications
Clinical and radiographic features of a family with autosomal dominant amelogenesis imperfecta with taurodontismM J Aldred
Department of Dentistry, Royal Children s Hospital, Melbourne, Australia
Oral Dis 8:62-8. 2002....- Amelogenesis imperfectaPeter J M Crawford
Paediatric Dentistry, Division of Child Dental Health, Dental School, Lower Maudlin St, Bristol BS1 2LY, UK
Orphanet J Rare Dis 2:17. 2007..In infancy, the primary dentition may be protected by the use of preformed metal crowns on posterior teeth. The longer-term care involves either crowns or, more frequently these days, adhesive, plastic restorations... - Oral medicine and oral pathology--the impact of electronic informationMichael J Aldred
Faculty of Oral Pathology, Royal College of Pathologists of Australasia, Surry Hills, New South Wales
Ann R Australas Coll Dent Surg 16:60-2. 2002..Without doubt these mechanisms will be further developed and refined in the present century... - It's only teeth - are there limits to genetic testing?M Aldred
Department of Dentistry, Royal Children s Hospital, Melbourne, Australia
Clin Genet 63:333-9. 2003..The questions we pose are whether these approaches are appropriate. We hope that this review will stimulate debate on these issues... - Amelogenesis imperfecta: a classification and catalogue for the 21st centuryM J Aldred
Department of Dentistry, Royal Children s Hospital, Melbourne, Australia
Oral Dis 9:19-23. 2003..We argue that this system is of more benefit to these individuals and families than previous classifications... - Molecular analysis for genetic counselling in amelogenesis imperfectaM J Aldred
Department of Dentistry, Royal Children s Hospital, Melbourne, Australia
Oral Dis 8:249-53. 2002..To use molecular genetics to establish the mode of inheritance in a family with amelogenesis imperfecta... - Identification of a locus on chromosome 2q11 at which recessive amelogenesis imperfecta and cone-rod dystrophy cosegregateLouise M Downey
Molecular Medicine Unit, CSB, St James s University Hospital, Leeds University, Leeds LS9 7TF UK
Eur J Hum Genet 10:865-9. 2002..It remains to be established whether this pedigree is segregating two closely linked mutations causing disparate phenotypes or whether a single defect is causing pathology in both teeth and eyes... - Enamel defects and Lyonization in focal dermal hypoplasiaRichard Balmer
Leeds Dental Institute, Leeds, United Kingdom
Oral Surg Oral Med Oral Pathol Oral Radiol Endod 98:686-91. 2004..This supports the proposal that focal dermal hypoplasia is X-linked. The authors conclude that the pattern of dental defects in focal dermal hypoplasia is consistent with Lyonization... - DLX3 mutation associated with autosomal dominant amelogenesis imperfecta with taurodontismJuan Dong
Department of Pediatric Dentistry, Dental School, University of Texas Health Science Center at San Antonio, 7703 Floyd Curl Drive, MC 7888, San Antonio, TX 78229, USA
Am J Med Genet A 133:138-41. 2005..Previous studies have shown a DLX3 mutation outside the homeodomain associated with tricho-dento-osseous syndrome (TDO) suggesting TDO and some forms of AIHHT are allelic... - Dental findings in a family with hyperparathyroidism-jaw tumor syndrome and a novel HRPT2 gene mutationMichael J Aldred
Dorevitch Pathology, Victoria 3084, Australia
Oral Surg Oral Med Oral Pathol Oral Radiol Endod 101:212-8. 2006..Cemento-ossifying fibroma is the preferred term to better reflect the pathologies found in most individuals and families,and to emphasize the significance of the jaw lesions in the diagnosis of the syndrome...