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Last Updated: 01/07/2026

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Found 211 publications

Genetic Variants in DVL3 are Associated With Root Maldevelopment, Tooth Agenesis, Mesiodens, and Oral Exostoses.

Genetic Variants in DVL3 are Associated With Root Maldevelopment, Tooth Agenesis, Mesiodens, and Oral Exostoses.

Journal: International dental journal
Published: August 31, 2025

Wnt5a gain- and loss-of-function present distinctly in craniofacial bone.

Wnt5a gain- and loss-of-function present distinctly in craniofacial bone.

Journal: bioRxiv : the preprint server for biology
Published: August 08, 2025

Wnt5a gain- and loss-of-function present distinctly in craniofacial bone.

Wnt5a gain- and loss-of-function present distinctly in craniofacial bone.

Journal: bioRxiv : the preprint server for biology
Published: August 08, 2025

Pathogenic DVL frameshifting variants in Robinow syndrome disrupt WNT signaling and cellular dynamics.

Pathogenic DVL frameshifting variants in Robinow syndrome disrupt WNT signaling and cellular dynamics.

Journal: bioRxiv : the preprint server for biology
Published: August 06, 2025

Nucleoredoxin regulates WNT signaling during pituitary stem cell differentiation.

Nucleoredoxin regulates WNT signaling during pituitary stem cell differentiation.

Journal: bioRxiv : the preprint server for biology
Published: February 20, 2025

Nucleoredoxin regulates WNT signaling during pituitary stem cell differentiation.

Nucleoredoxin regulates WNT signaling during pituitary stem cell differentiation.

Journal: Human molecular genetics
Published: February 04, 2025

Robinow syndrome DVL1 variants disrupt morphogenesis and appendage formation in a Drosophila disease model.

Robinow syndrome DVL1 variants disrupt morphogenesis and appendage formation in a Drosophila disease model.

Journal: Developmental dynamics : an official publication of the American Association of Anatomists
Published: December 20, 2024

Human Genetics of Ventricular Septal Defect.

Human Genetics of Ventricular Septal Defect.

Journal: Advances in experimental medicine and biology
Published: June 17, 2024

Fetal phenotype and diagnosis of autosomal dominant Robinow syndrome due to novel DVL1 variant.

Fetal phenotype and diagnosis of autosomal dominant Robinow syndrome due to novel DVL1 variant.

Journal: Prenatal diagnosis
Published: May 06, 2024

Prenatal diagnosis of ROR-2 related Robinow syndrome presenting with fetal ultrasound findings of mesomelia, vertebral, digital and genital abnormalities.

Prenatal diagnosis of ROR-2 related Robinow syndrome presenting with fetal ultrasound findings of mesomelia, vertebral, digital and genital abnormalities.

Journal: Prenatal diagnosis
Published: November 19, 2023

Craniofacial studies in chicken embryos confirm the pathogenicity of human FZD2 variants associated with Robinow syndrome.

Craniofacial studies in chicken embryos confirm the pathogenicity of human FZD2 variants associated with Robinow syndrome.

Journal: Disease models & mechanisms
Published: November 07, 2023

Non-canonical WNT5A-ROR signaling: New perspectives on an ancient developmental pathway.

Non-canonical WNT5A-ROR signaling: New perspectives on an ancient developmental pathway.

Journal: Current topics in developmental biology
Published: March 26, 2023
Showing 1-12 of 211

Last Updated: 01/07/2026