Meier-Gorlin Syndrome Latest Advances

Find the Latest Research About Meier-Gorlin Syndrome

Last Updated: 09/19/2026

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Found 99 publications

Revision Anterior Cruciate Ligament Reconstruction in an Adult Twin With Meier-Gorlin Syndrome.

Revision Anterior Cruciate Ligament Reconstruction in an Adult Twin With Meier-Gorlin Syndrome.

Journal: Ochsner journal
Published: June 18, 2026

Identification of a novel and a recurrent CDC45 variant in a Chinese family with Meier-Gorlin syndrome 7 and a literature review.

Identification of a novel and a recurrent CDC45 variant in a Chinese family with Meier-Gorlin syndrome 7 and a literature review.

Journal: Frontiers in genetics
Published: May 28, 2026

Endocrine Phenotypes and Hormonal Treatment in Meier-Gorlin Syndrome: Report of Two Cases and a Systematic Review of Literature.

Endocrine Phenotypes and Hormonal Treatment in Meier-Gorlin Syndrome: Report of Two Cases and a Systematic Review of Literature.

Journal: Clinical endocrinology
Published: May 04, 2026

A Meier-Gorlin syndrome mutation impairs the loading of the MCM2-7 complex during DNA replication initiation.

A Meier-Gorlin syndrome mutation impairs the loading of the MCM2-7 complex during DNA replication initiation.

Journal: Proceedings of the National Academy of Sciences of the United States of America
Published: February 20, 2026

Research advance on the clinical phenotypes and molecular genetic mechanisms of Microcephalic primordial dwarfism

Research advance on the clinical phenotypes and molecular genetic mechanisms of Microcephalic primordial dwarfism

Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: February 01, 2026

Bi-allelic WDHD1 variants cause microcephalic primordial dwarfism.

Bi-allelic WDHD1 variants cause microcephalic primordial dwarfism.

Journal: American journal of human genetics
Published: December 18, 2025

Molecular impacts of Meier-Gorlin syndrome mutations on human origin licensing.

Molecular impacts of Meier-Gorlin syndrome mutations on human origin licensing.

Journal: The Journal of biological chemistry
Published: November 16, 2025

Meier-Gorlin syndrome due to a recurrent DONSON variant in a Turkish family: first report of thumb aplasia and long-term growth data.

Meier-Gorlin syndrome due to a recurrent DONSON variant in a Turkish family: first report of thumb aplasia and long-term growth data.

Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: August 17, 2025

Anesthetic management in a child with Meier-Gorlin syndrome: a case report.

Anesthetic management in a child with Meier-Gorlin syndrome: a case report.

Journal: BMC anesthesiology
Published: August 01, 2025

Congenital Absence of Bilateral Patella in an Active Military Personnel Case Report.

Congenital Absence of Bilateral Patella in an Active Military Personnel Case Report.

Journal: Journal of orthopaedic case reports
Published: June 09, 2025

Unexpected molecular mechanism of Orc6-based Meier-Gorlin syndrome: insights from a humanized Drosophila model.

Unexpected molecular mechanism of Orc6-based Meier-Gorlin syndrome: insights from a humanized Drosophila model.

Journal: Genetics
Published: May 06, 2025

Diagnostic Yield of Exome Sequencing for Pregnancies With and Without Fetal Anomalies and for Stillbirth.

Diagnostic Yield of Exome Sequencing for Pregnancies With and Without Fetal Anomalies and for Stillbirth.

Journal: Prenatal diagnosis
Published: December 25, 2024
Showing 1-12 of 99

Last Updated: 09/19/2026