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PedAM

Pediatric Disease Annotations & Medicines




Disease dentinogenesis imperfecta
Phenotype C0031106|juvenile periodontitis
Sentences 1
PubMedID- 23633784 A linkage study on a dentinogenesis imperfecta-iii kindred with juvenile periodontitis (jp) has also suggested that this disease may be linked to the long arm (q) of human chromosome 4. furthermore, the autosomal domininant local hypoplastic form of amelogenesis imperfecta has also been recently linked to a 15.2 cm region of human chromosome 4 in the region 4q11-4q13.

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