Clara T. Chung
Randwick, NSW, Australia
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 10 publications
Multicystic Kidney Disease in a Family With Tuberous Sclerosis Complex.
Journal: Nephrology (Carlton, Vic.)
Published: August 27, 2025
Diagnosis and Management of Children With Tuberous Sclerosis Complex.
Journal: Journal of paediatrics and child health
Published: April 16, 2025
RICTOR variants are associated with neurodevelopmental disorders.
Journal: European journal of human genetics : EJHG
Published: August 01, 2024
Deep Sequencing and Phenotyping in an Australian Tuberous Sclerosis Complex "No Mutations Identified" Cohort.
Journal: Molecular genetics & genomic medicine
Published: June 27, 2024
A cell-based functional assay that accurately links genotype to phenotype in familial HLH.
Journal: Blood
Published: September 13, 2022
Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndrome.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: June 06, 2022
Congenital subpendymal giant cell astrocytoma in children with tuberous sclerosis complex: growth patterns and neurological outcome.
Journal: Pediatric research
Published: March 05, 2020
Gene selection for the Australian Reproductive Genetic Carrier Screening Project ("Mackenzie's Mission").
Journal: European journal of human genetics : EJHG
Published: February 13, 2020
RASA1 mosaic mutations in patients with capillary malformation-arteriovenous malformation.
Journal: Journal of medical genetics
Published: January 19, 2019
Early Detection of Tuberous Sclerosis Complex: An Opportunity for Improved Neurodevelopmental Outcome.
Journal: Pediatric neurology
Published: February 27, 2017
Showing 1-10 of 10
Last Updated: 09/26/2026