Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay.

Source:http://linkedlifedata.com/resource/pubmed/id/12605448

Am. J. Med. Genet. A 2003 Apr 1 118A 1 82-5

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PMID
12605448