Ulnar-Mammary Syndrome Latest Advances

TBX3- Related Disorder.

Journal: American journal of medical genetics. Part A

Published: May 08, 2025

An Unusual Mainly Skeletal Prenatal Presentation of Cornelia de Lange Syndrome Due To a Novel Variant in NIPBL.

Journal: Prenatal diagnosis

Published: April 07, 2025

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.

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

Ulnar-Mammary Syndrome Latest Advances

Find the Latest Research About Ulnar-Mammary Syndrome

TBX3- Related Disorder.

TBX3- Related Disorder.

An Unusual Mainly Skeletal Prenatal Presentation of Cornelia de Lange Syndrome Due To a Novel Variant in NIPBL.

An Unusual Mainly Skeletal Prenatal Presentation of Cornelia de Lange Syndrome Due To a Novel Variant in NIPBL.

Clinical and genetic analysis of ulnar-mammary syndrome caused by a novel TBX3 mutation in a Chinese boy.

Clinical and genetic analysis of ulnar-mammary syndrome caused by a novel TBX3 mutation in a Chinese boy.

Ancient developmental genes underlie evolutionary novelties in walking fish.

Ancient developmental genes underlie evolutionary novelties in walking fish.

An inherited TBX3 alteration in a prenatal case of ulnar-mammary syndrome: Clinical assessment and functional characterization in Drosophila melanogaster.

An inherited TBX3 alteration in a prenatal case of ulnar-mammary syndrome: Clinical assessment and functional characterization in Drosophila melanogaster.

A family with an atypical presentation of TBX3-related disorder.

A family with an atypical presentation of TBX3-related disorder.

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.

Ulnar-Mammary syndrome with TBX3 gene mutation in a Chinese family: A case report and literature review.

Ulnar-Mammary syndrome with TBX3 gene mutation in a Chinese family: A case report and literature review.

Structure of the endosomal Commander complex linked to Ritscher-Schinzel syndrome.

Structure of the endosomal Commander complex linked to Ritscher-Schinzel syndrome.

Literature review, report, and analysis of genotype and clinical phenotype of a rare case of ulnar-mammary syndrome.

Literature review, report, and analysis of genotype and clinical phenotype of a rare case of ulnar-mammary syndrome.

TBX3 and EFNA4 Variant in a Family with Ulnar-Mammary Syndrome and Sagittal Craniosynostosis.

TBX3 and EFNA4 Variant in a Family with Ulnar-Mammary Syndrome and Sagittal Craniosynostosis.

Mechanical loading is required for initiation of extracellular matrix deposition at the developing murine myotendinous junction.

Mechanical loading is required for initiation of extracellular matrix deposition at the developing murine myotendinous junction.