(Q46258979)

20 December 2017

title

Function of the Msx2 gene in the morphogenesis of the skull (English)

1 reference

20 December 2017

1 reference

Liu YH

1 reference

20 December 2017

Ma L

1 reference

20 December 2017

Kundu R

1 reference

20 December 2017

Ignelzi M

1 reference

20 December 2017

Sangiorgi F

1 reference

20 December 2017

Wu L

1 reference

20 December 2017

Luo W

1 reference

20 December 2017

Snead ML

1 reference

20 December 2017

Maxson R

1 reference

20 December 2017

language of work or name

English

0 references

publication date

1 June 1996

1 reference

20 December 2017

Annals of the New York Academy of Sciences

published in

1 reference

20 December 2017

volume

785

1 reference

20 December 2017

page(s)

48-58

1 reference

20 December 2017

Sutural biology and the correlates of craniosynostosis

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

The function and evolution of Msx genes: pointers and paradoxes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

Developmental expression of the endogenous TIMP gene and a TIMP-lacZ fusion gene in transgenic mice.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

Jackson-Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

Regulation of the Msx2 homeobox gene during mouse embryogenesis: a transgene with 439 bp of 5' flanking sequence is expressed exclusively in the apical ectodermal ridge of the developing limb

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

Premature suture closure and ectopic cranial bone in mice expressing Msx2 transgenes in the developing skull

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

Homeodomain Proteins: Cooperating to be different

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

Newly recognized autosomal dominant disorder with craniosynostosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1749-6632.1996.TB56243.X

10.1111/J.1749-6632.1996.TB56243.X

21 January 2018

Identifiers

DOI

1 reference

20 December 2017

1 reference

20 December 2017