Authors: | Bruneau S; Johnson KR; Yamamoto M; Kuroiwa A; Duboule D, 2001 [PMID:11543619] , Indexed by GXD, Spatially Mapped by EMAGE. |
Submitted by: | EMAGE EDITOR, Institute of Genetics and Molecular Medicine, Western General Hospital, Crewe Road, Edinburgh, UK EH4 2XU |
Experiment type: | non-screen |
References: | [ doi:10.1006/dbio.2001.0382] [ PMID:11543619] Bruneau S, Johnson KR, Yamamoto M, Kuroiwa A, Duboule D 2001 The mouse Hoxd13(spdh) mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes. Dev Biol (237):345-53 |
Links: | MGI:2153099 same experiment |
| Ensembl same gene |
| Allen Brain Atlas same gene |
| BioGPS same gene |
| International Mouse Knockout Project Status same gene |
| GEISHA Chicken ISH Database same gene |
| EMBL-EBI Gene Expression Atlas same gene |
| BrainStars same gene |
| ViBrism same gene |
Data Source |  |