(Q28507098)

24 January 2017

title

Mouse model of split hand/foot malformation type I (English)

1 reference

24 January 2017

main subject

Distal-less homeobox 6

1 reference

GOA release 2020-03-11

Distal-less homeobox 5

1 reference

GOA release 2020-03-11

Giorgio R. Merlo

1 reference

24 January 2017

Laura Paleari

1 reference

24 January 2017

Stefano Mantero

1 reference

24 January 2017

Francesca Genova

1 reference

24 January 2017

Annemiek Beverdam

1 reference

24 January 2017

Giulio L. Palmisano

1 reference

24 January 2017

Ottavia Barbieri

1 reference

24 January 2017

Giovanni Levi

1 reference

24 January 2017

publication date

1 June 2002

1 reference

24 January 2017

1 reference

24 January 2017

1 reference

24 January 2017

1 reference

24 January 2017

page(s)

97–101

1 reference

X-chromosomally inherited split-hand/split-foot anomaly in a Pakistani kindred.

24 January 2017

cites work

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10098

Heterozygous germline mutations in the p53 homolog p63 are the cause of EEC syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10098

Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10098

An epidemiological study of isolated split hand/foot in Hungary, 1975-1984.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10098

Targeted replacement of the homeobox gene Hox-3.1 by the Escherichia coli lacZ in mouse chimeric embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10098

A second autosomal split hand/split foot locus maps to chromosome 10q24-q25.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10098

Distal-less function during Drosophila appendage and sense organ development

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10098

Refined mapping of a gene for split hand-split foot malformation (SHFM3) on chromosome 10q25

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10098

Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10098

Distal limb malformations: underlying mechanisms and clinical associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10098

Cloning and characterization of two members of the vertebrate Dlx gene family

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10098

Split hand/split foot malformation with hearing loss: first report of families linked to the SHFM1 locus in 7q21.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10098

Heterodimerization of Msx and Dlx homeoproteins results in functional antagonism

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10098

On the inheritance of the split hand/split foot malformation

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10098

Dlx5 and Dlx6: an evolutionary conserved pair of murine homeobox genes expressed in the embryonic skeleton

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10098

inferred from DOI database lookup

7 January 2021

based on heuristic

A highly conserved enhancer in the Dlx5/Dlx6 intergenic region is the site of cross-regulatory interactions between Dlx genes in the embryonic forebrain.

1 reference

https://api.crossref.org/works/10.1002%2FGENE.10098

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1002/GENE.10098

0 references

1 reference