(Q33538468)

27 July 2017

1 reference

title

The genetic basis of normal and abnormal craniofacial development (English)

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27 July 2017

Thesleff I

1

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27 July 2017

language of work or name

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1 December 1998

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Acta Odontologica Scandinavica

27 July 2017

published in

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27 July 2017

volume

56

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27 July 2017

issue

6

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27 July 2017

page(s)

321-325

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Msx1 deficient mice exhibit cleft palate and abnormalities of craniofacial and tooth development

27 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1080%2F000163598428248

Null mutation of Dlx-2 results in abnormal morphogenesis of proximal first and second branchial arch derivatives and abnormal differentiation in the forebrain

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F000163598428248

Requirement for Lim1 in head-organizer function

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F000163598428248

Development of several organs that require inductive epithelial-mesenchymal interactions is impaired in LEF-1-deficient mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F000163598428248

Role of the Dlx homeobox genes in proximodistal patterning of the branchial arches: mutations of Dlx-1, Dlx-2, and Dlx-1 and -2 alter morphogenesis of proximal skeletal and soft tissue structures derived from the first and second arches

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F000163598428248

Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F000163598428248

Bone morphogenetic proteins in development

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F000163598428248

Tooth morphogenesis and cell differentiation

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F000163598428248

Fibroblast growth factors induce additional limb development from the flank of chick embryos

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F000163598428248

Vertebrate limb development

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F000163598428248

The bone morphogenetic protein family and osteogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F000163598428248

Mutations in the human Sonic Hedgehog gene cause holoprosencephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F000163598428248

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F000163598428248

A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F000163598428248

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/10.1080%2F000163598428248

Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F000163598428248

X-linked anhidrotic (hypohidrotic) ectodermal dysplasia is caused by mutation in a novel transmembrane protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F000163598428248

Cbfa1, a candidate gene for cleidocranial dysplasia syndrome, is essential for osteoblast differentiation and bone development

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F000163598428248

The Tabby phenotype is caused by mutation in a mouse homologue of the EDA gene that reveals novel mouse and human exons and encodes a protein (ectodysplasin-A) with collagenous domains

21 January 2018

1 reference

https://api.crossref.org/works/10.1080%2F000163598428248

21 January 2018

Identifiers

DOI

10.1080/000163598428248

1 reference

27 July 2017

1 reference