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Title
A novel AXIN2
gene mutation in sagittal synostosis
Authors
Keywords
-
Journal
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Volume 176, Issue 9, Pages 1976-1980
Publisher
Wiley
Online
2018-08-08
DOI
10.1002/ajmg.a.40373
References
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Related references
Note: Only part of the references are listed.- De novo mutations in inhibitors of Wnt, BMP, and Ras/ERK signaling pathways in non-syndromic midline craniosynostosis
- (2017) Andrew T. Timberlake et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Increase of prevalence of craniosynostosis
- (2016) Martijn Cornelissen et al. JOURNAL OF CRANIO-MAXILLOFACIAL SURGERY
- Stem cells of the suture mesenchyme in craniofacial bone development, repair and regeneration
- (2016) Takamitsu Maruyama et al. Nature Communications
- Understanding craniosynostosis as a growth disorder
- (2016) Kevin Flaherty et al. Wiley Interdisciplinary Reviews-Developmental Biology
- A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia
- (2015) Haochen Liu et al. PLoS One
- Partial trisomy 17q and partial monosomy 20q in a boy with craniosynostosis
- (2014) Felipe Marques et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Craniosynostosis
- (2012) S. Nagaraja et al. CLINICAL RADIOLOGY
- Cranial Suture Biology
- (2012) Benjamin Levi et al. JOURNAL OF CRANIOFACIAL SURGERY
- Changing Epidemiology of Nonsyndromic Craniosynostosis and Revisiting the Risk Factors
- (2012) Hui Qing Lee et al. JOURNAL OF CRANIOFACIAL SURGERY
- Nonsyndromic Craniosynostosis
- (2012) Rebecca Garza et al. Seminars in Plastic Surgery
- Differential activation of canonical Wnt signaling determines cranial sutures fate: A novel mechanism for sagittal suture craniosynostosis
- (2010) Björn Behr et al. DEVELOPMENTAL BIOLOGY
- Prevalence and Complications of Single-Gene and Chromosomal Disorders in Craniosynostosis
- (2010) A. O. M. Wilkie et al. PEDIATRICS
- The Balance of WNT and FGF Signaling Influences Mesenchymal Stem Cell Fate During Skeletal Development
- (2010) T. Maruyama et al. Science Signaling
- Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis
- (2008) N. Callahan et al. ARCHIVES OF ORAL BIOLOGY
- AXIN2andCDH1polymorphisms, tooth agenesis, and oral clefts
- (2008) Ariadne Letra et al. BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
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