Myelomeningocele and Waardenburg syndrome (type 3) in patients with interstitial deletions of 2q35 and the PAX3 gene: possible digenic inheritance of a neural tube defect.

Source:http://linkedlifedata.com/resource/pubmed/id/9482647

Am. J. Med. Genet. 1998 Feb 3 75 4 401-8

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PMID
9482647