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Last Updated: 10/31/2025
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Found 8 publications
Multiple rhabdomyomatous mesenchymal hamartomas in a patient with mosaic Barber-Say syndrome.
Journal: Pediatric dermatology
Published: January 24, 2023
Ocular adnexal phenotype and management of a patient with mosaic expression of a mutation in TWIST2.
Ocular adnexal phenotype and management of a patient with mosaic expression of a mutation in TWIST2.
Journal: Orbit (Amsterdam, Netherlands)
Published: June 07, 2021
Barber Say Syndrome (A New Case Report).
Journal: Indian dermatology online journal
Published: April 16, 2019
Multidisciplinary eyelid reconstruction in Barber-Say syndrome: A case report.
Journal: Archivos de la Sociedad Espanola de Oftalmologia
Published: August 23, 2018
Clinical Description, Molecular Analysis of TWIST2 Gene, and Surgical Treatment in a Patient With Barber-Say Syndrome.
Journal: Ophthalmic plastic and reconstructive surgery
Published: January 13, 2018
Transmission of Barber-Say syndrome from a mosaic father to his child in an Indian family.
Journal: Clinical dysmorphology
Published: April 20, 2016
Barber-Say syndrome and Ablepharon-Macrostomia syndrome: An overview.
Journal: American journal of medical genetics. Part A
Published: March 11, 2016
Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes.
Journal: American journal of human genetics
Published: April 06, 2015
Showing 1-8 of 8
Last Updated: 10/31/2025