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Whole-exome sequencing, without prior linkage, identifies a mutation in LAMB3 as a cause of dominant hypoplastic amelogenesis imperfecta

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author: James A Poulter  Alan J. Mighell  Jennifer Kirkham  Chris F. Inglehearn  Walid El-Sayed 

Publication date May 1, 2013
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http://eprints.whiterose.ac.uk/75574/

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