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Clin Genet. 2009 Apr;75(4):401-4. doi: 10.1111/j.1399-0004.2008.01112.x. Epub 2009 Feb 11.

Novel FAM83H mutations in Turkish families with autosomal dominant hypocalcified amelogenesis imperfecta.

PMID:
19220331
PMCID:
PMC4264522
DOI:
10.1111/j.1399-0004.2008.01112.x
[PubMed - indexed for MEDLINE]
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