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Last Updated: 10/31/2025
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Found 54 publications
Clinical Features of Gollop-Wolfgang Complex in North Africa: A Case Study.
Journal: Cureus
Published: July 13, 2025
Gollop-Wolfgang Complex Is Associated with a Monoallelic Variation in WNT11.
Journal: Genes
Published: December 17, 2023
A case report of Gollop-Wolfgang complex in 12 years old boy.
Journal: International journal of surgery case reports
Published: February 22, 2023
Fatty filum terminale and low-lying conus medullaris in Gollop-Wolfgang complex: a case report and review of literature.
Journal: Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery
Published: August 02, 2022
SHFLD3 phenotypes caused by 17p13.3 triplication/ duplication encompassing Fingerin (BHLHA9) invariably.
Journal: Orphanet journal of rare diseases
Published: March 23, 2022
Newborn Male With Fibular Aplasia, Tibial Campomelia, and Oligosyndactyly Syndrome: A New Case Report Putting the Condition Under Spotlight.
Journal: Cureus
Published: January 28, 2022
Gollop-Wolfgang Complex: Clinical and Imaging Implications.
Journal: The Indian journal of radiology & imaging
Published: November 18, 2021
A rare case of limb deficiency syndrome: Gollop WolfGang syndrome.
Journal: Radiology case reports
Published: May 02, 2021
Split hand/foot malformation with long bone deficiency associated with BHLHA9 gene duplication: a case report and review of literature.
Journal: BMC medical genetics
Published: February 11, 2019
Last Updated: 10/31/2025