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Last Updated: 01/07/2026
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Found 48 publications
Clinical and operative risk factors for complications after Apert hand syndactyly reconstruction.
Journal: The Journal of hand surgery, European volume
Published: November 21, 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
A novel autosomal recessive GJA1 missense mutation linked to Craniometaphyseal dysplasia.
Journal: PloS one
Published: April 24, 2013
Congenital heart defects in oculodentodigital dysplasia: Report of two cases.
Journal: American journal of medical genetics. Part A
Published: February 24, 2013
Genetic heterogeneity in type III familial cutaneous syndactyly and linkage to chromosome 7q36.
Journal: American journal of medical genetics. Part A
Published: November 08, 2012
Last Updated: 01/07/2026