Syndactyly Type 3 Latest Advances

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

Clinical and operative risk factors for complications after Apert hand syndactyly reconstruction.

Journal: The Journal of hand surgery, European volume

Published: November 21, 2023

Webplasty using an external fixator for complex syndactyly caused by Apert syndrome.

Journal: Journal of orthopaedic science : official journal of the Japanese Orthopaedic Association

Published: October 23, 2023

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

Journal: Annals of plastic surgery

Published: March 07, 2023

Apert syndrome: a rare clinical image.

Journal: The Pan African medical journal

Published: January 17, 2023

Developments in the Diagnosis and Therapeutic Strategy of the Apert Hand

Journal: Handchirurgie, Mikrochirurgie, plastische Chirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft fur Handchirurgie : Organ der Deutschsprachigen Arbeitsgemeinschaft fur Mikrochirurgie der Peripheren Nerven und Gefasse : Organ der V...

Published: June 10, 2022

Acrosyndactyly: Are we using the term correctly?

Journal: Journal of plastic, reconstructive & aesthetic surgery : JPRAS

Published: May 29, 2020

Apert syndrome - clinical case.

Journal: Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie

Published: May 20, 2017

A de novo 2q35-q36.1 deletion incorporating IHH in a Chinese boy (47,XYY) with syndactyly, type III Waardenburg syndrome, and congenital heart disease.

Journal: Genetics and molecular research : GMR

Published: December 15, 2016

Oculodentodigital dysplasia with massive brain calcification and a new mutation of GJA1 gene.

Journal: Journal of Alzheimer's disease : JAD

Published: October 08, 2015

Dermatoglyphics in kidney diseases: a review.

Journal: SpringerPlus

Published: August 18, 2015

A novel autosomal recessive GJA1 missense mutation linked to Craniometaphyseal dysplasia.

Journal: PloS one

Published: April 24, 2013

Syndactyly Type 3 Latest Advances

Find the Latest Research About Syndactyly Type 3

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.

Clinical and operative risk factors for complications after Apert hand syndactyly reconstruction.

Clinical and operative risk factors for complications after Apert hand syndactyly reconstruction.

Webplasty using an external fixator for complex syndactyly caused by Apert syndrome.

Webplasty using an external fixator for complex syndactyly caused by Apert syndrome.

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.

Apert syndrome: a rare clinical image.

Apert syndrome: a rare clinical image.

Developments in the Diagnosis and Therapeutic Strategy of the Apert Hand

Developments in the Diagnosis and Therapeutic Strategy of the Apert Hand

Acrosyndactyly: Are we using the term correctly?

Acrosyndactyly: Are we using the term correctly?

Apert syndrome - clinical case.

Apert syndrome - clinical case.

A de novo 2q35-q36.1 deletion incorporating IHH in a Chinese boy (47,XYY) with syndactyly, type III Waardenburg syndrome, and congenital heart disease.

A de novo 2q35-q36.1 deletion incorporating IHH in a Chinese boy (47,XYY) with syndactyly, type III Waardenburg syndrome, and congenital heart disease.

Oculodentodigital dysplasia with massive brain calcification and a new mutation of GJA1 gene.

Oculodentodigital dysplasia with massive brain calcification and a new mutation of GJA1 gene.

Dermatoglyphics in kidney diseases: a review.

Dermatoglyphics in kidney diseases: a review.

A novel autosomal recessive GJA1 missense mutation linked to Craniometaphyseal dysplasia.

A novel autosomal recessive GJA1 missense mutation linked to Craniometaphyseal dysplasia.