Syndactyly Type 2 Latest Advances

HOXD12 a candidate gene for a novel form of synpolydactyly.

Journal: Bone

Published: December 10, 2025

Absence of Syndactyly Associated With the Common Apert FGFR2 S252W Mutation: A Clinical Report and Likely Molecular Explanation.

Journal: American journal of medical genetics. Part A

Published: June 01, 2025

Long-Read Whole-Genome Sequencing Uncovers a Deletion Upstream to HOXD13 Causing Synpolydactyly.

Journal: American journal of medical genetics. Part A

Published: April 21, 2025

Central Ray Synpolydactyly with Bilateral Medial Foot Polydactyly and Hydrocephalus: A Case Report.

Journal: Plastic and reconstructive surgery. Global open

Published: February 04, 2025

Unraveling the Genetic Basis of Congenital Limb Anomalies in Eight Families.

Journal: Clinical genetics

Published: September 12, 2024

The Intrarater and Interrater Reliability of the OMT Classification Among Physicians With a Different Background.

Journal: Journal of pediatric orthopedics

Published: April 26, 2024

Biophysical and structural studies of fibulin-2.

Journal: Scientific reports

Published: February 21, 2024

New insight into the development of synpolydactyly caused by expansion of HOXD13 polyalanine based on weighted gene co-expression network analysis.

Journal: BMC medical genomics

Published: September 04, 2023

Paralog-specific TTC30 regulation of Sonic hedgehog signaling.

Journal: Frontiers in molecular biosciences

Published: July 28, 2023

Novel mutation c.2090_2091del in neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities in an 18.5-mo-old boy: A case report.

Journal: World journal of clinical cases

Published: March 14, 2023

An Evolution of the Surgical Management of Synpolydactyly: A Case Series of 21 Hands.

Journal: Annals of plastic surgery

Published: March 07, 2023

HOXD13-associated synpolydactyly: Extending and validating the genotypic and phenotypic spectrum with 38 new and 49 published families.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: January 31, 2023

Syndactyly Type 2 Latest Advances

Find the Latest Research About Syndactyly Type 2

HOXD12 a candidate gene for a novel form of synpolydactyly.

HOXD12 a candidate gene for a novel form of synpolydactyly.

Absence of Syndactyly Associated With the Common Apert FGFR2 S252W Mutation: A Clinical Report and Likely Molecular Explanation.

Absence of Syndactyly Associated With the Common Apert FGFR2 S252W Mutation: A Clinical Report and Likely Molecular Explanation.

Long-Read Whole-Genome Sequencing Uncovers a Deletion Upstream to HOXD13 Causing Synpolydactyly.

Long-Read Whole-Genome Sequencing Uncovers a Deletion Upstream to HOXD13 Causing Synpolydactyly.

Central Ray Synpolydactyly with Bilateral Medial Foot Polydactyly and Hydrocephalus: A Case Report.

Central Ray Synpolydactyly with Bilateral Medial Foot Polydactyly and Hydrocephalus: A Case Report.

Unraveling the Genetic Basis of Congenital Limb Anomalies in Eight Families.

Unraveling the Genetic Basis of Congenital Limb Anomalies in Eight Families.

The Intrarater and Interrater Reliability of the OMT Classification Among Physicians With a Different Background.

The Intrarater and Interrater Reliability of the OMT Classification Among Physicians With a Different Background.

Biophysical and structural studies of fibulin-2.

Biophysical and structural studies of fibulin-2.

New insight into the development of synpolydactyly caused by expansion of HOXD13 polyalanine based on weighted gene co-expression network analysis.

New insight into the development of synpolydactyly caused by expansion of HOXD13 polyalanine based on weighted gene co-expression network analysis.

Paralog-specific TTC30 regulation of Sonic hedgehog signaling.

Paralog-specific TTC30 regulation of Sonic hedgehog signaling.

Novel mutation c.2090_2091del in neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities in an 18.5-mo-old boy: A case report.

Novel mutation c.2090_2091del in neurodevelopmental-craniofacial syndrome with variable renal and cardiac abnormalities in an 18.5-mo-old boy: A case report.

An Evolution of the Surgical Management of Synpolydactyly: A Case Series of 21 Hands.

An Evolution of the Surgical Management of Synpolydactyly: A Case Series of 21 Hands.

HOXD13-associated synpolydactyly: Extending and validating the genotypic and phenotypic spectrum with 38 new and 49 published families.

HOXD13-associated synpolydactyly: Extending and validating the genotypic and phenotypic spectrum with 38 new and 49 published families.