(Q36890936)

16 August 2017

1 reference

title

Genetic analysis of non-syndromic craniosynostosis (English)

1 reference

16 August 2017

0 references

S A Boyadjiev

1

1 reference

PubMed ID

17651129

16 August 2017

International Craniosynostosis Consortium

series ordinal

2

1 reference

16 August 2017

1 August 2007

1 reference

Orthodontics & Craniofacial Research

16 August 2017

1 reference

16 August 2017

10

1 reference

16 August 2017

3

1 reference

16 August 2017

129-137

1 reference

Genetic heterogeneity of Saethre-Chotzen syndrome, due to TWIST and FGFR mutations.

16 August 2017

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Genetic analysis of patients with the Saethre-Chotzen phenotype.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Craniosynostosis. I. Sagittal synostosis: its genetics and associated clinical findings in 214 patients who lacked involvement of the coronal suture(s)

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Genetic study of scaphocephaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Maternal smoking and craniosynostosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Craniosynostosis. II. Coronal synostosis: its familial characteristics and associated clinical findings in 109 patients lacking bilateral polysyndactyly or syndactyly.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Genetic study of nonsyndromic coronal craniosynostosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Syndromal and nonsyndromal primary trigonocephaly: analysis of a series of 237 patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

The differential diagnosis of posterior plagiocephaly: true lambdoid synostosis versus positional molding

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Genetic and environmental risk factors for sagittal craniosynostosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Prevalence of Pro250Arg mutation of fibroblast growth factor receptor 3 in coronal craniosynostosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Two craniosynostotic patients with 11q deletions, and review of 48 cases.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Chromosome breakage hotspots and delineation of the critical region for the 9p-deletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Craniosynostosis: genes and mechanisms

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Mutations in TWIST, a basic helix-loop-helix transcription factor, in Saethre-Chotzen syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Revisiting the craniosynostosis-radial ray hypoplasia association: Baller-Gerold syndrome caused by mutations in the RECQL4 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Precision and error of three-dimensional phenotypic measures acquired from 3dMD photogrammetric images.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Brain morphology in nonsyndromic unicoronal craniosynostosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

Central nervous system phenotypes in craniosynostosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

The International HapMap Project

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1601-6343.2007.00393.X

10.1111/J.1601-6343.2007.00393.X

21 January 2018

Identifiers

DOI

1 reference

16 August 2017

1 reference

PubMed ID

17651129