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

Author： Bruneau S.   Johnson K.R.   Yamamoto M.   Kuroiwa A.   Duboule D.  

Publisher： Academic Press

ISSN： 0012-1606

Source： Developmental Biology, Vol.237, Iss.2, 2001-09, pp. : 345-353

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