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Last Updated: 10/31/2025
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Found 101 publications
Clinical and genetic analysis of ulnar-mammary syndrome caused by a novel TBX3 mutation in a Chinese boy.
Journal: Intractable & rare diseases research
Published: December 29, 2024
Ancient developmental genes underlie evolutionary novelties in walking fish.
Journal: Current biology : CB
Published: June 07, 2024
An inherited TBX3 alteration in a prenatal case of ulnar-mammary syndrome: Clinical assessment and functional characterization in Drosophila melanogaster.
Journal: Journal of cellular physiology
Published: March 11, 2024
A family with an atypical presentation of TBX3-related disorder.
Journal: European journal of medical genetics
Published: February 20, 2024
Generalized Verrucosis on a Background of 3C Syndrome Treated With Subcutaneous IgG Supplementation.
Generalized Verrucosis on a Background of 3C Syndrome Treated With Subcutaneous IgG Supplementation.
Journal: JAMA dermatology
Published: October 18, 2023
Ulnar-Mammary syndrome with TBX3 gene mutation in a Chinese family: A case report and literature review.
Journal: Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences
Published: February 07, 2023
Structure of the endosomal Commander complex linked to Ritscher-Schinzel syndrome.
Journal: Cell
Published: January 12, 2023
Literature review, report, and analysis of genotype and clinical phenotype of a rare case of ulnar-mammary syndrome.
Journal: Frontiers in pediatrics
Published: September 24, 2022
TBX3 and EFNA4 Variant in a Family with Ulnar-Mammary Syndrome and Sagittal Craniosynostosis.
Journal: Genes
Published: August 24, 2022
Mechanical loading is required for initiation of extracellular matrix deposition at the developing murine myotendinous junction.
Journal: Matrix biology : journal of the International Society for Matrix Biology
Published: June 26, 2022
Last Updated: 10/31/2025