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The Mouse Hoxd13spdh Mutation, a Polyalanine Expansion Similar to Human Type II Synpolydactyly (SPD), Disrupts the Function but Not the Expression of Other Hoxd Genes

By Sylvia Bruneau, Kenneth R. Johnson, Masakazu Yamamoto, Atsushi Kuroiwa and Denis Duboule
Publisher: Elsevier BV
Year: 2002
DOI identifier: 10.1006/dbio.2001.0382
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Provided by: MUCC (Crossref)
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