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Amelogenesis imperfecta type 2
- ... Registry: Amelogenesis imperfecta, hypocalcification type Genetic Testing Registry: Amelogenesis imperfecta type 1C Genetic Testing Registry: Amelogenesis imperfecta type 1E ...
- ... form of a disorder of tooth development called amelogenesis imperfecta. Autosomal recessive inheritance means that two copies of the MMP20 gene in each cell ...
- ... FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta. Am J Hum Genet. 2008 Feb;82(2):489-94. doi: 10.1016/j.ajhg.2007. ...
- ... COL17A1 in non-Herlitz junctional epidermolysis bullosa and amelogenesis imperfecta. Int J Mol Med. 2006 Aug;18(2):333-7. Citation on PubMed Pasmooij AM, Pas ...