(Q46687481)

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A hole in the head

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scholarly article

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Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/10742087

A hole in the head (English)

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/10742087

author name string

Ferguson MW

1

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/10742087

language of work or name

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publication date

1 April 2000

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/10742087

Nature Genetics

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Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/10742087

24

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/10742087

4

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/10742087

330-331

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/10742087

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

1 reference

https://api.crossref.org/works/10.1038%2F74132

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F74132

7 January 2021

based on heuristic

inferred from DOI database lookup

MSX1 mutation is associated with orofacial clefting and tooth agenesis in humans

1 reference

https://api.crossref.org/works/10.1038%2F74132

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F74132

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1038%2F74132

7 January 2021

based on heuristic

inferred from DOI database lookup

A human MSX1 homeodomain missense mutation causes selective tooth agenesis

1 reference

https://api.crossref.org/works/10.1038%2F74132

7 January 2021

based on heuristic

inferred from DOI database lookup

Association of MSX1 and TGFB3 with nonsyndromic clefting in humans

1 reference

https://api.crossref.org/works/10.1038%2F74132

7 January 2021

based on heuristic

inferred from DOI database lookup

Transforming growth factor-beta 3 is required for secondary palate fusion

1 reference

https://api.crossref.org/works/10.1038%2F74132

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/10742087

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

24 December 2017

http://europepmc.org/abstract/MED/10742087

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