Mutations in the humanTWIST gene
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Reference27 articles.
1. Recommendations for a nomenclature system for human gene mutations
2. The mapping of a gene for craniosynostosis: evidence for linkage of the Saethre-Chotzen syndrome to distal chromosome 7p.
3. The myogenic regulatory gene Mef2 is a direct target for transcriptional activation by Twist during Drosophila myogenesis
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1. Tcf12 controls dynamic calvarial bone growth and motor learning in mice;2024-01-09
2. Postnatal Progressive Craniosynostosis in Syndromic Conditions: Two Patients With Saethre-Chotzen Due to TWIST1 Gene Deletions and Review of the Literature;The Cleft Palate-Craniofacial Journal;2022-03-30
3. De novo ALX4 variant detected in child with non-syndromic craniosynostosis;Brazilian Journal of Medical and Biological Research;2021
4. Cranial Suture Regeneration Mitigates Skull and Neurocognitive Defects in Craniosynostosis;Cell;2021-01
5. Lateral and Frontal Cephalometric Measurements in a Cohort With Saethre-Chotzen Syndrome;The Cleft Palate-Craniofacial Journal;2020-11-06
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