Quantification of facial skeletal shape variation in fibroblast growth factor receptor‐related craniosynostosis syndromes-Reference-Cited by-同舟云学术

Quantification of facial skeletal shape variation in fibroblast growth factor receptor‐related craniosynostosis syndromes

Published:2014-02-27 Issue:4 Volume:100 Page:250-259
ISSN:1542-0752
Container-title:Birth Defects Research Part A: Clinical and Molecular Teratology
language:en
Short-container-title:Birth Defects Research

Author:

Heuzé Yann¹,Martínez‐Abadías Neus¹,Stella Jennifer M.¹,Arnaud Eric²,Collet Corinne³,García Fructuoso Gemma⁴,Alamar Mariana⁴,Lo Lun‐Jou⁵,Boyadjiev Simeon A.⁶,Di Rocco Federico²,Richtsmeier Joan T.¹

Affiliation:

1. Department of AnthropologyPennsylvania State UniversityUniversity Park Pennsylvania

2. Craniofacial Surgery Unit, Department of Pediatric NeurosurgeryHôpital Necker‐Enfants Malades, University Paris VParis France

3. Laboratoire de Biochimie et de Biologie Moléculaire, INSERM U606Paris France

4. Servei de Neurocirurgia, Hospital Sant Joan de DéuBarcelona Spain

5. Department of Plastic and Reconstructive SurgeryChang Gung Memorial Hospital, Chang Gung UniversityTaoyuan Taiwan

6. Section of Genetics, Department of PediatricsUniversity of California DavisSacramento California

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/bdra.23228

Reference51 articles.

1. Elements of morphology: Standard terminology for the head and face

2. Apert syndrome mutations in fibroblast growth factor receptor 2 exhibit increased affinity for FGF ligand

3. Amphioxus FGF signaling predicts the acquisition of vertebrate morphological traits

4. Landmark methods for forms without landmarks: morphometrics of group differences in outline shape

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