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Last Updated: 10/31/2025
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Found 1160 publications
A Child With Cleidocranial Dysplasia Presenting With Seizure Disorder.
Journal: Cureus
Published: August 10, 2025
A Chinese premature infant with cleidocranial dysplasia characterized by heterozygous RUNX2 mutation and cerebral infarction: a case report.
Journal: Frontiers in pediatrics
Published: June 11, 2025
Skeletal dysplasias-Multidisciplinary orthopedics
Journal: Orthopadie (Heidelberg, Germany)
Published: June 05, 2025
Cleidocranial Dysplasia: A Case Report Highlighting Dental, Craniofacial, and Skeletal Complexity.
Journal: Clinical case reports
Published: May 21, 2025
Identification and splicing analysis of the first deep intronic FIG4 variant causing Yunis-Varon syndrome.
Journal: Frontiers in genetics
Published: May 08, 2025
Downregulation of Nesprin1 by Runx2 deficiency is critical for the development of skeletal laminopathy-like pathology.
Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: April 10, 2025
Disturbances of Dental Development in Cleidocranial Dysplasia.
Journal: The Journal of craniofacial surgery
Published: February 22, 2025
Neonatal Familiar Cleidocranial Dysplasia: A Case Report.
Journal: The American journal of case reports
Published: January 26, 2025
Unveiling Cleidocranial Dysplasia: An Antenatal Journey Through Ultrasound and Delivering the Importance of Taking Phenotype History; "Echoes of the Past".
Journal: Journal of clinical ultrasound : JCU
Published: January 15, 2025
Clinicoradiological findings in a case of cleidocranial dysplasia.
Journal: BMJ case reports
Published: July 29, 2024
Last Updated: 10/31/2025