Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 4 of 4 for Amelogenesis imperfecta type 2
  1. ... Registry: Amelogenesis imperfecta, hypocalcification type Genetic Testing Registry: Amelogenesis imperfecta type 1C Genetic Testing Registry: Amelogenesis imperfecta type 1E ...
  2. ... form of a disorder of tooth development called amelogenesis imperfecta. Autosomal recessive inheritance means that two copies of the MMP20 gene in each cell ...
  3. ... 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. ...
  4. ... 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 ...