(Q34230565)

31 July 2017

Split hand foot malformation is associated with a reduced level of Dactylin gene expression (English)

1 reference

31 July 2017

1 reference

Basel D

1

1 reference

31 July 2017

DePaepe A

series ordinal

2

1 reference

31 July 2017

Kilpatrick MW

series ordinal

3

1 reference

31 July 2017

Tsipouras P

series ordinal

4

1 reference

31 July 2017

language of work or name

1 reference

1 October 2003

1 reference

31 July 2017

1 reference

31 July 2017

64

1 reference

31 July 2017

350-354

1 reference

31 July 2017

4

1 reference

Cloning, chromosomal organization and expression analysis of Neurl, the mouse homolog of Drosophila melanogaster neuralized gene

31 July 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00153.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00153.X

7 January 2021

Mapping of the gene for X-chromosomal split-hand/split-foot anomaly to Xq26-q26.1.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00153.X

7 January 2021

Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00153.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00153.X

7 January 2021

Fine mapping of the split-hand/split-foot locus (SHFM3) at 10q24: evidence for anticipation and segregation distortion.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00153.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00153.X

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00153.X

7 January 2021

Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00153.X

7 January 2021

Dactylaplasia in mice a two-locus model for development anomalies

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00153.X

7 January 2021

Mapping the mouse dactylaplasia mutation, Dac, and a gene that controls its expression, mdac

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00153.X

7 January 2021

A novel human gene encoding an F-box/WD40 containing protein maps in the SHFM3 critical region on 10q24

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00153.X

7 January 2021

A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00153.X

7 January 2021

Genomic organization and embryonic expression of Suppressor of Fused, a candidate gene for the split-hand/split-foot malformation type 3.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00153.X

7 January 2021

Defect in the maintenance of the apical ectodermal ridge in the Dactylaplasia mouse

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00153.X

7 January 2021

The gene for triphalangeal thumb maps to the subtelomeric region of chromosome 7q.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2003.00153.X

7 January 2021

10.1034/J.1399-0004.2003.00153.X

Identifiers

DOI

1 reference

31 July 2017

1 reference