(Q48610943)

13 February 2018

title

Mutation in the FGFR2 gene in a Taiwanese patient with Beare-Stevenson cutis gyrata syndrome. (English)

1 reference

13 February 2018

Beare-Stevenson cutis gyrata syndrome

main subject

0 references

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6

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13 February 2018

author name string

Wang TJ

1

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13 February 2018

Huang CB

2

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13 February 2018

Tsai FJ

3

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13 February 2018

Wu JY

4

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13 February 2018

Lai RB

5

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13 February 2018

publication date

1 March 2002

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13 February 2018

published in

Clinical Genetics

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13 February 2018

volume

61

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13 February 2018

issue

3

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13 February 2018

page(s)

218-221

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13 February 2018

Beare-Stevenson cutis gyrata syndrome

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610309.X

A cloverleaf skull syndrome probably of Beare-Stevenson type associated with Chiari malformation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610309.X

Fibroblast growth factor receptor 2 mutations in Beare-Stevenson cutis gyrata syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610309.X

Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610309.X

Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610309.X

FGFR2 mutations in Pfeiffer syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610309.X

Crystal structures of two FGF-FGFR complexes reveal the determinants of ligand-receptor specificity

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610309.X

Effective indirect pulp capping (Cp-treatment)

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610309.X

7 January 2021

A severe case of Beare-Stevenson syndrome and associated congenital deformities

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610309.X

7 January 2021

FGFR2 gene mutation (Tyr375Cys) in a new case of Beare-Stevenson syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610309.X

7 January 2021

Jackson-Weiss syndrome: identification of two novel FGFR2 missense mutations shared with Crouzon and Pfeiffer craniosynostotic disorders

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.2002.610309.X

7 January 2021

10.1034/J.1399-0004.2002.610309.X

Identifiers

DOI

1 reference

13 February 2018

1 reference

13 February 2018