(Q40434670)

20 September 2017

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title

Perspectives on craniofacial asymmetry. V. The craniosynostoses (English)

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20 September 2017

Cohen MM Jr

1

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20 September 2017

language of work or name

English

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publication date

1 June 1995

1 reference

International Journal of Oral and Maxillofacial Surgery

20 September 2017

published in

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20 September 2017

volume

24

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20 September 2017

issue

3

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20 September 2017

page(s)

191-194

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Craniostenosis: A review of the etiology and a report of new cases

20 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0901-5027%2806%2980125-6

7 January 2021

Craniosynostosis update 1987.

1 reference

https://api.crossref.org/works/10.1016%2FS0901-5027%2806%2980125-6

7 January 2021

Sutural biology and the correlates of craniosynostosis

1 reference

https://api.crossref.org/works/10.1016%2FS0901-5027%2806%2980125-6

7 January 2021

The central nervous system in the Apert syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0901-5027%2806%2980125-6

7 January 2021

Birth prevalence studies of the Crouzon syndrome: comparison of direct and indirect methods

1 reference

https://api.crossref.org/works/10.1016%2FS0901-5027%2806%2980125-6

7 January 2021

Growth pattern in the Apert syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0901-5027%2806%2980125-6

7 January 2021

Hands and feet in the Apert syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0901-5027%2806%2980125-6

7 January 2021

Birth prevalence study of the Apert syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0901-5027%2806%2980125-6

7 January 2021

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/10.1016%2FS0901-5027%2806%2980125-6

7 January 2021

Comparative three-dimensional analysis of CT-scans of the calvaria and cranial base in Apert and Crouzon syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0901-5027%2806%2980125-6

7 January 2021

Genetic heterogeneity among craniosynostosis syndromes: mapping the Saethre-Chotzen syndrome locus between D7S513 and D7S516 and exclusion of Jackson-Weiss and Crouzon syndrome loci from 7p

1 reference

https://api.crossref.org/works/10.1016%2FS0901-5027%2806%2980125-6

7 January 2021

Two craniosynostotic syndrome loci, Crouzon and Jackson-Weiss, map to chromosome 10q23-q26

1 reference

https://api.crossref.org/works/10.1016%2FS0901-5027%2806%2980125-6

7 January 2021

A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10.

1 reference

https://api.crossref.org/works/10.1016%2FS0901-5027%2806%2980125-6

7 January 2021

Linkage of Pfeiffer syndrome to chromosome 8 centromere and evidence for genetic heterogeneity

1 reference

https://api.crossref.org/works/10.1016%2FS0901-5027%2806%2980125-6

7 January 2021

GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families

1 reference

https://api.crossref.org/works/10.1016%2FS0901-5027%2806%2980125-6

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0901-5027%2806%2980125-6

7 January 2021

10.1016/S0901-5027(06)80125-6

Identifiers

DOI

1 reference

20 September 2017

1 reference