(Q44960264)

7 December 2017

title

RUNX2 gene status in a cleidocranial dysplasia patient without supernumerary teeth (English)

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7 December 2017

main subject

cleidocranial dysplasia

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Robert P Anthonappa

1

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7 December 2017

Nigel M King

series ordinal

2

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7 December 2017

Abou-Bakr Mahmoud Rabie

series ordinal

3

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7 December 2017

publication date

27 November 2012

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Journal of investigative and clinical dentistry

7 December 2017

published in

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7 December 2017

volume

4

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7 December 2017

issue

2

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7 December 2017

page(s)

124-127

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Mutations involving the transcription factor CBFA1 cause cleidocranial dysplasia

7 December 2017

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJICD.12019

Mutations in the RUNX2 gene in patients with cleidocranial dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJICD.12019

Functional analysis of RUNX2 mutations in cleidocranial dysplasia: novel insights into genotype–phenotype correlations

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJICD.12019

RUNX2 mutations in cleidocranial dysplasia patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJICD.12019

Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJICD.12019

21 January 2018

Identifiers

DOI

10.1111/JICD.12019

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7 December 2017

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