Shuk C. Chong
Sar, China
Last Updated: 09/26/2026
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Found 17 publications
Third-trimester prenatal brain imaging for early diagnosis of glutaric aciduria type 1 in monochorionic diamniotic twins.
Journal: Hong Kong medical journal = Xianggang yi xue za zhi
Published: January 26, 2026
Population-scale genomic medicine with the Hong Kong Genome Project.
Journal: Nature medicine
Published: September 09, 2025
Fragile X syndrome: genetic and clinical profile in the Hong Kong Chinese population.
Journal: Hong Kong medical journal = Xianggang yi xue za zhi
Published: June 05, 2025
Implementation of Public Funded Genome Sequencing in Evaluation of Fetal Structural Anomalies.
Journal: Genes
Published: October 25, 2022
The view of Hong Kong parents on secondary use of dried blood spots in newborn screening program.
Journal: BMC medical ethics
Published: June 30, 2022
Expansion of the clinical and molecular spectrum of WWOX-related epileptic encephalopathy.
Journal: American journal of medical genetics. Part A
Published: June 12, 2022
Case Report: Novel Biallelic Variants in the COL18A1 Gene in a Chinese Family With Knobloch Syndrome.
Journal: Frontiers in neurology
Published: January 13, 2022
Expanded carrier screening using next-generation sequencing of 123 Hong Kong Chinese families: a pilot study.
Journal: Hong Kong medical journal = Xianggang yi xue za zhi
Published: February 19, 2021
Low-pass genome sequencing: a validated method in clinical cytogenetics.
Journal: Human genetics
Published: March 11, 2020
Severe Generalized Epidermolysis Bullosa Simplex in Two Hong Kong Children due to De Novo Variants in KRT14 and KRT5.
Journal: Case reports in pediatrics
Published: December 17, 2019
Neonatal epidermolysis bullosa: lessons to learn about genetic counseling.
Journal: The Journal of dermatological treatment
Published: October 04, 2018
Last Updated: 09/26/2026