(Q34306402)

1 August 2017

1 reference

title

Syndromes involving craniosynostosis and midface hypoplasia (English)

1 reference

1 August 2017

0 references

Katzen JT

1

1 reference

PubMed ID

11449786

1 August 2017

McCarthy JG

series ordinal

2

1 reference

1 August 2017

1 December 2000

1 reference

Otolaryngologic Clinics of North America

1 August 2017

1 reference

1 August 2017

33

1 reference

1 August 2017

1257-84, vi

1 reference

1 August 2017

6

1 reference

Facial asymmetry and abnormalties of palms and ears: A dominantly inherited developmental syndrome

1 August 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Apert's syndrome (a type of acrocephalosyndactyly)-observations on a British series of thirty-nine cases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Chronic tonsillar herniation in Crouzon's and Apert's syndromes: the role of premature synostosis of the lambdoid suture

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

The central nervous system in the Apert syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

New indirect method for estimating the birth prevalence of the Apert syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Upper and lower airway compromise in the Apert syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Growth pattern in the Apert syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Skeletal abnormalities in the Apert syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

A clinical study of the craniofacial features in Apert syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Birth prevalence study of the Apert syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Analysis of the mutational spectrum of the FGFR2 gene in Pfeiffer syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Saethre-Chotzen syndrome: A broad and variable pattern of skeletal malformations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

A study of intracranial volume in Apert syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Morbidity associated with increased intracranial pressure in Apert and Pfeiffer syndromes: the need for long-term evaluation.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Obstructive sleep apnea syndrome and its treatment in children: areas of agreement and controversy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Epidemiological aspects of Mendelian syndromes in a Spanish population sample: II. Autosomal recessive malformation syndromes

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Early Surgery for Craniofacial Synostosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Le Fort III advancement osteotomy in the growing child

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

7 January 2021

Saethre-Chotzen syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Surgical management of the cloverleaf skull deformity

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Favorable prognosis for children with Pfeiffer syndrome types 2 and 3: implications for classification

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Mutations in FGFR1 and FGFR2 cause familial and sporadic Pfeiffer syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Saethre-Chotzen syndrome associated with balanced translocations involving 7p21: three further families

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

Surgical correction of Crouzon syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

inferred from DOI database lookup

7 January 2021

based on heuristic

Early surgery for craniofacial synostosis: an 8-year experience

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

inferred from DOI database lookup

7 January 2021

based on heuristic

Advancement of the orbits and the midface in one piece, combined with frontal repositioning, for the correction of Crouzon's deformities

1 reference

https://api.crossref.org/works/10.1016%2FS0030-6665%2805%2970280-2

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1016/S0030-6665(05)70280-2

1 reference

1 August 2017

1 reference

PubMed ID

11449786