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-Reference-Cited by-同舟云学术

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

Published:2001-09 Issue:2 Volume:237 Page:345-353
ISSN:0012-1606
Container-title:Developmental Biology
language:en
Short-container-title:Developmental Biology

Author:

Bruneau Sylvia,Johnson Kenneth R.,Yamamoto Masakazu,Kuroiwa Atsushi,Duboule Denis

Publisher

Elsevier BV

Subject

Cell Biology,Developmental Biology,Molecular Biology

Reference30 articles.

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3. Absence of radius and ulna in mice lacking Hoxa11 and Hoxd11;Davis;Nature,1995

4. Coordinate expression of the murine HOX-5 homeobox containing gene during limb pattern formation;Dollé;Nature,1989

5. Disruption of the Hoxd-13 gene induces localized heterochrony leading to mice with neotenic limbs;Dollé;Cell,1993

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