Robinow Syndrome Latest Advances

Find the Latest Research About Robinow Syndrome

Last Updated: 02/24/2026

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Found 213 publications

Local Misalignment Scoring Reveals Spatially Uniform Chondrocyte Disorganization in a Wnt5a-C83S Knock-in Model of Robinow Syndrome.

Local Misalignment Scoring Reveals Spatially Uniform Chondrocyte Disorganization in a Wnt5a-C83S Knock-in Model of Robinow Syndrome.

Journal: Research square
Published: January 09, 2026

Robinow Syndrome Mimicking Congenital Adrenal Hyperplasia.

Robinow Syndrome Mimicking Congenital Adrenal Hyperplasia.

Journal: JCEM case reports
Published: November 10, 2025

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
Showing 1-12 of 213

Last Updated: 02/24/2026