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ArticleAmerican journal of human genetics1995

Further elucidation of the genomic structure of PAX3, and identification of two different point mutations within the PAX3 homeobox that cause Waardenburg syndrome type 1 in two families.

A K Lalwani et al.PubMed ↗Full text ↗

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Full record →Abstract, authors, funding and every citing paper · PMID 7825605