A novel AXIN2 gene mutation in sagittal synostosis
Author:
Affiliation:
1. Department of Medical Biology and GeneticsAkdeniz University, School of Medicine Antalya Turkey
2. Department of Pediatric GeneticsAkdeniz University, School of Medicine Antalya Turkey
Funder
Akdeniz Üniversitesi
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.40373
Reference34 articles.
1. Craniosynostosis
2. Differential activation of canonical Wnt signaling determines cranial sutures fate: A novel mechanism for sagittal suture craniosynostosis
3. Axis inhibition protein 2 (AXIN2) polymorphisms and tooth agenesis
4. Genetic perspectives on craniosynostosis and syndromes with craniosynostosis
5. Editorial: Perspectives on craniosynostosis
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1. Clinical interest of molecular study in cases of isolated midline craniosynostosis;European Journal of Human Genetics;2023-02-03
2. Craniofacial sutures: Signaling centres integrating mechanosensation, cell signaling, and cell differentiation;European Journal of Cell Biology;2022-06
3. Sagittal Synostosis and Its Association With Cognitive, Behavioral, and Psychological Functioning;JAMA Network Open;2021-09-13
4. Cranial Suture Mesenchymal Stem Cells: Insights and Advances;Biomolecules;2021-07-31
5. An Axin2 mutation and perinatal risk factors contribute to sagittal craniosynostosis: evidence from a Chinese female monochorionic diamniotic twin family;Hereditas;2021-06-16
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