Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2 (Q55670708)

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Language	Label	Description	Also known as
English	Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2	article

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instance of

scholarly article

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title

Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2 (English)

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main subject

Parietal foramina with cleidocranial dysplasia

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author

Andrew Oliver Mungo Wilkie

object named as

Andrew O M Wilkie

series ordinal

7

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author name string

Sixto Garcia-Miñaur

series ordinal

1

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Lampros A Mavrogiannis

series ordinal

2

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Sahan V Rannan-Eliya

series ordinal

3

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Michael A Hendry

series ordinal

4

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William A Liston

series ordinal

5

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Mary E M Porteous

series ordinal

6

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language of work or name

English

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publication date

November 2003

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published in

European Journal of Human Genetics

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volume

11

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issue

11

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page(s)

892-5

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cites work

Functional haploinsufficiency of the human homeobox gene MSX2 causes defects in skull ossification

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201062

retrieved

21 January 2018

Identification of mutations in the MSX2 homeobox gene in families affected with foramina parietalia permagna

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201062

retrieved

21 January 2018

The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201062

retrieved

21 January 2018

Haploinsufficiency of the human homeobox gene ALX4 causes skull ossification defects

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201062

retrieved

21 January 2018

Mutations in the RUNX2 gene in patients with cleidocranial dysplasia

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201062

retrieved

21 January 2018

Derivation of the mammalian skull vault

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201062

retrieved

21 January 2018

Development of the clavicles in birds and mammals

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201062

retrieved

21 January 2018

Mouse clavicular development: Analysis of wild-type and cleidocranial dysplasia mutant mice

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201062

retrieved

21 January 2018

Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation

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stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201062

retrieved

21 January 2018

Parietal foramina in Saethre-Chotzen syndrome.

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201062

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Parietal foramina clavicular hypoplasia. An autosomal dominant syndrome

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201062

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1038/SJ.EJHG.5201062

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Dimensions Publication ID

1047192362

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PubMed publication ID

14571277

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ResearchGate publication ID

231586497

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