(Q30991204)

28 June 2017

title

Clinical features of hereditary progressive arthro-ophthalmopathy (Stickler syndrome): a survey (English)

1 reference

28 June 2017

1 reference

Stickler GB

1

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28 June 2017

Hughes W

series ordinal

2

1 reference

28 June 2017

Houchin P

series ordinal

3

1 reference

28 June 2017

language of work or name

English

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publication date

1 May 2001

1 reference

28 June 2017

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28 June 2017

volume

3

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28 June 2017

issue

3

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28 June 2017

page(s)

192-196

1 reference

https://scigraph.springernature.com/pub.10.1097/00125817-200105000-00008

28 June 2017

exact match

0 references

cites work

Genetics and hearing loss: a review of Stickler syndrome

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00008

The type XI collagenopathies.

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00008

21 January 2018

Hereditary vitreopathy

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00008

Molecular basis of heritable connective tissue disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00008

Weissenbacher-Zweymüller syndrome: a distinct autosomal recessive skeletal dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00008

Splicing mutations of 54-bp exons in the COL11A1 gene cause Marshall syndrome, but other mutations cause overlapping Marshall/Stickler phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00008

The Wagner-Stickler syndrome: A study of 22 families

21 January 2018

1 reference

https://api.crossref.org/works/10.1097%2F00125817-200105000-00008

10.1097/00125817-200105000-00008

21 January 2018

Identifiers

DOI

1 reference

Dimensions Publication ID

28 June 2017

1005410432

0 references

1 reference