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Last Updated: 10/31/2025
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Found 7 publications
Identification of a novel variant of SCARF2 in a Jordanian family with a van den Ende-Gupta Syndrome and literature review.
Journal: Clinical dysmorphology
Published: March 08, 2022
Two novel variants in SCARF2 gene underlie van den Ende-Gupta syndrome.
Journal: American journal of medical genetics. Part A
Published: December 25, 2020
Further delineation of van den Ende-Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndrome.
Journal: American journal of medical genetics. Part A
Published: November 30, 2020
Inclusion of joint laxity, recurrent patellar dislocation, and short distal ulnae as a feature of Van Den Ende-Gupta syndrome: a case report.
Journal: BMC medical genetics
Published: October 09, 2017
Diagnosis of Van den Ende-Gupta syndrome: Approach to the Marden-Walker-like spectrum of disorders.
Journal: American journal of medical genetics. Part A
Published: November 19, 2015
Expanding the clinical spectrum and allelic heterogeneity in van den Ende-Gupta syndrome.
Journal: Clinical genetics
Published: May 02, 2013
Vector control in internal midface distraction using temporary anchorage devices.
Journal: The Journal of craniofacial surgery
Published: November 17, 2012
Showing 1-7 of 7
Last Updated: 10/31/2025