Acrofacial Dysostosis Nager Type Latest Advances

Towards consensus on the treatment of congenital craniofacial conditions: the discussion section of a doctoral thesis.

Journal: Journal of plastic surgery and hand surgery

Published: February 16, 2026

Nager Syndrome Revisited: Integrating In Vivo and In Vitro Models to Decipher SF3B4-Dependent Tissue Coordination.

Journal: WIREs mechanisms of disease

Published: August 18, 2025

In silico analysis identified potential interaction between glutathione and spliceosome in Nager Syndrome.

Journal: Free radical biology & medicine

Published: May 29, 2025

PTBP3 Associated With 9q32 Locus Is a Candidate Gene for Nager Syndrome.

Journal: Birth defects research

Published: May 29, 2025

The Development of a European Registry for Facial Dysostosis Syndromes: A Delphi-Guided Approach.

Journal: The Journal of craniofacial surgery

Published: March 25, 2025

Unveiling the Phenotypic Spectrum of Miller Syndrome: A Systematic Review.

Journal: The Journal of craniofacial surgery

Published: March 03, 2025

A New Case of Nager Syndrome as a Rare Cause of Acrofacial Dysostosis.

Journal: Molecular syndromology

Published: December 05, 2024

Complete Agenesis of Right Half of Soft Palate-A Case Report.

Journal: Indian journal of plastic surgery : official publication of the Association of Plastic Surgeons of India

Published: November 18, 2024

Deletion of sf3b4 causes splicing defects and gene dysregulation that disrupt craniofacial development and survival.

Journal: Disease models & mechanisms

Published: October 23, 2024

Management and Outcomes of Neonates with Treacher Collins and Nager Syndromes.

Journal: The Journal of pediatrics

Published: October 04, 2024

Human stem cell model of neural crest cell differentiation reveals a requirement of SF3B4 in survival, maintenance, and differentiation.

Journal: Developmental dynamics : an official publication of the American Association of Anatomists

Published: May 01, 2024

Sf3b4 mutation in Xenopus tropicalis causes RNA splicing defects followed by massive gene dysregulation that disrupt cranial neural crest development.

Journal: bioRxiv : the preprint server for biology

Published: February 14, 2024

Acrofacial Dysostosis Nager Type Latest Advances

Find the Latest Research About Acrofacial Dysostosis Nager Type

Towards consensus on the treatment of congenital craniofacial conditions: the discussion section of a doctoral thesis.

Towards consensus on the treatment of congenital craniofacial conditions: the discussion section of a doctoral thesis.

Nager Syndrome Revisited: Integrating In Vivo and In Vitro Models to Decipher SF3B4-Dependent Tissue Coordination.

Nager Syndrome Revisited: Integrating In Vivo and In Vitro Models to Decipher SF3B4-Dependent Tissue Coordination.

In silico analysis identified potential interaction between glutathione and spliceosome in Nager Syndrome.

In silico analysis identified potential interaction between glutathione and spliceosome in Nager Syndrome.

PTBP3 Associated With 9q32 Locus Is a Candidate Gene for Nager Syndrome.

PTBP3 Associated With 9q32 Locus Is a Candidate Gene for Nager Syndrome.

The Development of a European Registry for Facial Dysostosis Syndromes: A Delphi-Guided Approach.

The Development of a European Registry for Facial Dysostosis Syndromes: A Delphi-Guided Approach.

Unveiling the Phenotypic Spectrum of Miller Syndrome: A Systematic Review.

Unveiling the Phenotypic Spectrum of Miller Syndrome: A Systematic Review.

A New Case of Nager Syndrome as a Rare Cause of Acrofacial Dysostosis.

A New Case of Nager Syndrome as a Rare Cause of Acrofacial Dysostosis.

Complete Agenesis of Right Half of Soft Palate-A Case Report.

Complete Agenesis of Right Half of Soft Palate-A Case Report.

Deletion of sf3b4 causes splicing defects and gene dysregulation that disrupt craniofacial development and survival.

Deletion of sf3b4 causes splicing defects and gene dysregulation that disrupt craniofacial development and survival.

Management and Outcomes of Neonates with Treacher Collins and Nager Syndromes.

Management and Outcomes of Neonates with Treacher Collins and Nager Syndromes.

Human stem cell model of neural crest cell differentiation reveals a requirement of SF3B4 in survival, maintenance, and differentiation.

Human stem cell model of neural crest cell differentiation reveals a requirement of SF3B4 in survival, maintenance, and differentiation.

Sf3b4 mutation in Xenopus tropicalis causes RNA splicing defects followed by massive gene dysregulation that disrupt cranial neural crest development.

Sf3b4 mutation in Xenopus tropicalis causes RNA splicing defects followed by massive gene dysregulation that disrupt cranial neural crest development.