(Q50958600)

26 March 2018

title

WNT1 mutation with recessive osteogenesis imperfecta and profound neurological phenotype. (English)

1 reference

26 March 2018

main subject

osteogenesis imperfecta

0 references

3

Fowzan S Alkuraya

1 reference

26 March 2018

2

Ranad Shaheen

1 reference

26 March 2018

author name string

Eissa Faqeih

series ordinal

1

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26 March 2018

language of work or name

English

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publication date

24 May 2013

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26 March 2018

Journal of Medical Genetics

published in

1 reference

26 March 2018

volume

50

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26 March 2018

issue

7

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26 March 2018

page(s)

491-492

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26 March 2018

Mutations in WNT1 cause different forms of bone fragility

cites work

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101750

WNT1 mutations in families affected by moderately severe and progressive recessive osteogenesis imperfecta

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101750

The Wnt-1 (int-1) proto-oncogene is required for development of a large region of the mouse brain

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101750

Study of autosomal recessive osteogenesis imperfecta in Arabia reveals a novel locus defined by TMEM38B mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1136%2FJMEDGENET-2013-101750

10.1136/JMEDGENET-2013-101750

21 January 2018

Identifiers

DOI

1 reference

26 March 2018

PubMed ID

23709755

1 reference

26 March 2018